Academic

Jon Ellman

Chemistry · 0000-0001-9320-5512 · Yale University

Citations received by year

Google Scholar profile

Series: Citations received.0500100015002000250030001994 Citations received 2021995 Citations received 2751996 Citations received 6241997 Citations received 7591998 Citations received 8881999 Citations received 10272000 Citations received 10012001 Citations received 10022002 Citations received 11512003 Citations received 13142004 Citations received 13642005 Citations received 13442006 Citations received 15282007 Citations received 15972008 Citations received 15892009 Citations received 19842010 Citations received 19692011 Citations received 22132012 Citations received 23322013 Citations received 27562014 Citations received 29922015 Citations received 29622016 Citations received 28082017 Citations received 26322018 Citations received 25302019 Citations received 23532020 Citations received 20792021 Citations received 21582022 Citations received 18922023 Citations received 16512024 Citations received 16452025 Citations received 15922026 Citations received 10721994200020052010201520202026Citations receivedCalendar year
Series: Citations received.0500100015002000250030001994 Citations received 2021995 Citations received 2751996 Citations received 6241997 Citations received 7591998 Citations received 8881999 Citations received 10272000 Citations received 10012001 Citations received 10022002 Citations received 11512003 Citations received 13142004 Citations received 13642005 Citations received 13442006 Citations received 15282007 Citations received 15972008 Citations received 15892009 Citations received 19842010 Citations received 19692011 Citations received 22132012 Citations received 23322013 Citations received 27562014 Citations received 29922015 Citations received 29622016 Citations received 28082017 Citations received 26322018 Citations received 25302019 Citations received 23532020 Citations received 20792021 Citations received 21582022 Citations received 18922023 Citations received 16512024 Citations received 16452025 Citations received 15922026 Citations received 10721994200020052010201520202026Citations receivedCalendar year

Citations received in each calendar year across this verified Scholar profile. Bars are annual counts; missing years are unknown. 2026 is an incomplete calendar year.

Publications

394 rows, 15 from the Scholar profile only, 92 need review

Scholar profile verified; its publication list is only partly imported (300 records fetched). Publication-based totals may be incomplete. The annual citation chart uses the profile’s separate citation history.

2026 Biocatalytic Enantioselective Oxidation of N-Acyl-S-Methyl Sulfenamides for the Asymmetric Synthesis of S-Methyl Sulfoximines Organic Letters article journal CV OA GS

CV span

lines 100–102 · CV · published

1002. Patel, S.; Finnigan, J. D.; Lim, J.; Greenwood, N. S.; Ellman, J. A. “Biocatalytic Enantioselective101Oxidation of N-Acyl-S-Methyl Sulfenamides for the Asymmetric Synthesis of S-Methyl102Sulfoximines” Org. Lett. 28, 304-309 (2026).

Institution fields

Peer reviewed
yes
First author
Patel
Co-authors
Patel, S.; Finnigan, J. D.; Lim, J.; Greenwood, N. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Biocatalytic Enantioselective Oxidation of N-Acyl-S-Methyl Sulfenamides for the Asymmetric Synthesis of S-Methyl SulfoximinesBiocatalytic Enantioselective Oxidation of N -Acyl- S -Methyl Sulfenamides for the Asymmetric Synthesis of S -Methyl Sulfoximines
year cv 20262025
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.5c0470110.1021/acs.orglett.5c04701
first author openalex PatelPatel

Citations

OpenAlex
3
Scholar
none
DOI
10.1021/acs.orglett.5c04701
OpenAlex
W4417519249

Match decisions

  • doi merged · 1.00 · Run 18
2026 Visible Light Promoted Alkenyl C–H Bond Addition to Dienes and Aldehydes for the Synthesis of Frameworks Relevant to Polyketide Natural Products ACS Catalysis article journal CV OA GS

CV span

lines 95–98 · CV · published

951. Ohno, S.; Goodner, R. M.;Confair, D. N.; Mercado, B. Q.; Ellman, J. A. “Visible Light Promoted96Alkenyl C–H Bond Addition to Dienes and Aldehydes for the Synthesis of Frameworks Relevant to97Polyketide Natural Products” ACS Catal. 15, ASAP (2026).98https://pubs.acs.org/doi/10.1021/acscatal.5c05961

Institution fields

Peer reviewed
yes
First author
Ohno
Co-authors
Ohno, S.; Goodner, R. M.; Confair, D. N.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Visible Light Promoted Alkenyl C–H Bond Addition to Dienes and Aldehydes for the Synthesis of Frameworks Relevant to Polyketide Natural ProductsVisible Light Promoted Alkenyl C–H Bond Addition to Dienes and Aldehydes for the Synthesis of Frameworks Relevant to Polyketide Natural Products
year cv 20262025
venue crossref ACS Catal.ACS CatalysisACS Catalysis
kind cv articlearticle
DOI cv 10.1021/acscatal.5c0596110.1021/acscatal.5c05961
first author openalex OhnoOhno

Citations

OpenAlex
1
Scholar
none
DOI
10.1021/acscatal.5c05961
OpenAlex
W7117255197

Match decisions

  • doi merged · 1.00 · Run 18
2025 Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects ACS Central Science article journal CV OA GS

CV span

lines 108–112 · CV · published

1084. Vigneron, S. F.; Ohno, S.; Braz, J.; Kim, J. Y.; Kweon, O. S.; Webb, C.; Billesbølle, C. B.;109Srinivasan, K.; Bhardwaj, K.; Irwin, J. J.; Manglik, A.; Basbaum, A. I.; Ellman, J. A.; Shoichet, B.110K. “Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals111Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects” ACS Cent. Sci. 11, 770–790112(2025).

Institution fields

Peer reviewed
yes
First author
Vigneron
Co-authors
Vigneron, S. F.; Ohno, S.; Braz, J.; Kim, J. Y.; Kweon, O. S.; Webb, C.; Billesbølle, C. B.; Srinivasan, K.; Bhardwaj, K.; Irwin, J. J.; Manglik, A.; Basbaum, A. I.; Ellman, J. A.; Shoichet, B. K.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal EffectsDocking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effectsDocking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
year cv 202520252025
venue crossref ACS Cent. Sci.bioRxiv (Cold Spring Harbor Laboratory)ACS Central ScienceACS Central Science
kind cv articleworking_paperarticle
DOI crossref 10.1021/acscentsci.5c0005210.1101/2025.01.09.63203310.1021/acscentsci.5c00052
preprint DOI openalex 10.1101/2025.01.09.632033
first author openalex VigneronVigneronVigneron

Citations

OpenAlex
10
Scholar
none
OpenAlex with related records
13
DOI
10.1021/acscentsci.5c00052
OpenAlex
W4409916335

Match decisions

  • doi merged · 1.00 · Run 18
2025 Ruthenium-Catalyzed Enantioselective Alkylation of Sulfenamides: A General Approach for the Synthesis of Drug Relevant S-Methyl and S-Cyclopropyl Sulfoximines Journal of the American Chemical Society article journal CV OA GS

CV span

lines 114–116 · CV · published

1145. Boyer, Z. W.; Kwon, N. Y.; Ellman, J. A.; Gnamm, C. “Ruthenium-Catalyzed Enantioselective115Alkylation of Sulfenamides: A General Approach for the Synthesis of Drug Relevant S-Methyl and116S-Cyclopropyl Sulfoximines” J. Am. Chem. Soc. 147, 14954–14959 (2025).

Institution fields

Peer reviewed
yes
First author
Boyer
Co-authors
Boyer, Z. W.; Kwon, N. Y.; Ellman, J. A.; Gnamm, C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Ruthenium-Catalyzed Enantioselective Alkylation of Sulfenamides: A General Approach for the Synthesis of Drug Relevant S-Methyl and S-Cyclopropyl SulfoximinesRuthenium-Catalyzed Enantioselective Alkylation of Sulfenamides: A General Approach for the Synthesis of Drug Relevant S -Methyl and S -Cyclopropyl SulfoximinesRuthenium-catalyzed enantioselective alkylation of sulfenamides: A general approach for the synthesis of drug relevant S-methyl and S-cyclopropyl sulfoximines
year cv 202520252025
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.5c0384110.1021/jacs.5c03841
first author openalex BoyerBoyerBoyer

Citations

OpenAlex
44
Scholar
40
DOI
10.1021/jacs.5c03841
OpenAlex
W4409868524

Match decisions

  • doi merged · 1.00 · Run 18
2025 Studies on the Mechanism of Styrene Elimination from Sulfilimines: Hammett and Kinetic Isotope Effect Analysis and Computation The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 104–106 · CV · published

1043. Patel, S.; Cerny, N. P.; Zimmer, L. G.; Chen, S.; Ellman, J. A. “Studies on the Mechanism of105Styrene Elimination from Sulfilimines: Hammett and Kinetic Isotope Effect Analysis and106Computation” J. Org. Chem. 90, 11597–11604 (2025).

Institution fields

Peer reviewed
yes
First author
Patel
Co-authors
Patel, S.; Cerny, N. P.; Zimmer, L. G.; Chen, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Studies on the Mechanism of Styrene Elimination from Sulfilimines: Hammett and Kinetic Isotope Effect Analysis and ComputationStudies on the Mechanism of Styrene Elimination from Sulfilimines: Hammett and Kinetic Isotope Effect Analysis and Computation
year cv 20252025
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/acs.joc.5c0122810.1021/acs.joc.5c01228
first author openalex PatelPatel

Citations

OpenAlex
3
Scholar
none
DOI
10.1021/acs.joc.5c01228
OpenAlex
W4412792701

Match decisions

  • doi merged · 1.00 · Run 18
2025 Sulfilimines from a Medicinal Chemist’s Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 118–122 · CV · published

1186. Greenwood, N. S.; Boyer, Z. W.; Ellman, J. A.; Gnamm, C. “Sulfilimines from a Medicinal119Chemist’s Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery” J.120Med. Chem. 68, 4079–4100 (2025) [Feature Article with a Viewpoint by Prof. Arvidsson121“Sulfilimines: An Underexplored Bioisostere for Drug Design?” J. Med. Chem. 68, 4056–4058122(2025)].

Institution fields

Peer reviewed
yes
First author
Greenwood
Co-authors
Greenwood, N. S.; Boyer, Z. W.; Ellman, J. A.; Gnamm, C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Sulfilimines from a Medicinal Chemist’s Perspective: Physicochemical and in Vitro Parameters Relevant for Drug DiscoverySulfilimines from a Medicinal Chemist’s Perspective: Physicochemical and in Vitro Parameters Relevant for Drug DiscoverySulfilimines from a medicinal chemist’s perspective: physicochemical and in vitro parameters relevant for drug discovery
year cv 202520252025
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.jmedchem.4c0271410.1021/acs.jmedchem.4c02714
first author openalex GreenwoodGreenwoodGreenwood

Citations

OpenAlex
50
Scholar
49
DOI
10.1021/acs.jmedchem.4c02714
OpenAlex
W4406207660

Match decisions

  • doi merged · 1.00 · Run 18
2024 C–H Activation and Sequential Addition to Dienes and Imines: Synthesis of Amines with β-Quaternary Centers and Mechanistic Studies on the Complex Interplay Between the Catalyst and Three Reactants ACS Catalysis article journal CV OA GS

CV span

lines 124–127 · CV · published

1247. Goodner, R. M.; Brandes, D. S.; Morais, G. N.; Tao, Q.; Tassone, J. P.; Mercado, B. Q.; Chen, S.;125Ellman, J. A. “C–H Activation and Sequential Addition to Dienes and Imines: Synthesis of Amines126with β-Quaternary Centers and Mechanistic Studies on the Complex Interplay Between the Catalyst127and Three Reactants” ACS Catal. 14, 18124–18133 (2024).

Institution fields

Peer reviewed
yes
First author
Goodner
Co-authors
Goodner, R. M.; Brandes, D. S.; Morais, G. N.; Tao, Q.; Tassone, J. P.; Mercado, B. Q.; Chen, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv C–H Activation and Sequential Addition to Dienes and Imines: Synthesis of Amines with β-Quaternary Centers and Mechanistic Studies on the Complex Interplay Between the Catalyst and Three ReactantsC–H Activation and Sequential Addition to Dienes and Imines: Synthesis of Amines with β-Quaternary Centers and Mechanistic Studies on the Complex Interplay Between the Catalyst and Three Reactants
year cv 20242024
venue crossref ACS Catal.ACS CatalysisACS Catalysis
kind cv articlearticle
DOI crossref 10.1021/acscatal.4c0586610.1021/acscatal.4c05866
first author openalex GoodnerGoodner

Citations

OpenAlex
9
Scholar
none
DOI
10.1021/acscatal.4c05866
OpenAlex
W4404650722

Match decisions

  • doi merged · 1.00 · Run 18
2024 Copper-Catalyzed Three-Component Synthesis of Highly Substituted Morpholines Organic Letters article journal CV OA GS

CV span

lines 146–147 · CV · published

14613. Chu, D.; Zoll, A. J.; Ellman, J. A. “Copper-Catalyzed Three-Component Synthesis of Highly147Substituted Morpholines” Org. Lett. 26, 4803–4807 (2024).

Institution fields

Peer reviewed
yes
First author
Chu
Co-authors
Chu, D.; Zoll, A. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Copper-Catalyzed Three-Component Synthesis of Highly Substituted MorpholinesCopper-Catalyzed Three-Component Synthesis of Highly Substituted Morpholines
year cv 20242024
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.4c0163410.1021/acs.orglett.4c01634
first author openalex ChuChu

Citations

OpenAlex
9
Scholar
none
DOI
10.1021/acs.orglett.4c01634
OpenAlex
W4399116838

Match decisions

  • doi merged · 1.00 · Run 18
2024 Disulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wide ACS Chemical Biology article journal CV OA GS

CV span

lines 135–137 · CV · published

13510. Moon, M. H.; Vock, I. W.; Streit, A. D.; Connor, L. J.; Senkina, J.; Ellman, J. A.; Simon, M. D.136“Disulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wide” ASC Chem. Biol.13719, 2081–2086 (2024).

Institution fields

Peer reviewed
yes
First author
Moon
Co-authors
Moon, M. H.; Vock, I. W.; Streit, A. D.; Connor, L. J.; Senkina, J.; Ellman, J. A.; Simon, M. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Disulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wideDisulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wide
year cv 20242024
venue crossref ASC Chem. Biol.ACS Chemical BiologyACS Chemical Biology
kind cv articlearticle
DOI crossref 10.1021/acschembio.4c0053810.1021/acschembio.4c00538
first author openalex MoonMoon

Citations

OpenAlex
4
Scholar
none
DOI
10.1021/acschembio.4c00538
OpenAlex
W4401959876

Match decisions

  • doi merged · 1.00 · Run 18
2024 Enantioselective S-Alkylation of Sulfenamides by Phase-Transfer Catalysis Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 139–140 · CV · published

13911. Champlin, A. T.; Kwon, N. Y.; Ellman, J. A. “Enantioselective S-Alkylation of Sulfenamides by140Phase-Transfer Catalysis” Angew. Chem. Int. Ed. 63, e202408820 (2024).

Institution fields

Peer reviewed
yes
First author
Champlin
Co-authors
Champlin, A. T.; Kwon, N. Y.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective S-Alkylation of Sulfenamides by Phase-Transfer CatalysisEnantioselective S‐Alkylation of Sulfenamides by Phase‐Transfer CatalysisEnantioselective S‐Alkylation of Sulfenamides by Phase‐Transfer CatalysisEnantioselective S‐Alkylation of Sulfenamides by Phase‐Transfer Catalysis
year cv 2024202420242024
venue crossref Angew. Chem. Int. Ed.Angewandte ChemieAngewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20240882010.1002/ange.20240882010.1002/anie.202408820
first author openalex ChamplinChamplinChamplinChamplin

Also recorded as

Citations

OpenAlex
52
Scholar
69
DOI
10.1002/anie.202408820
OpenAlex
W4401019496

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2024 Rh(II)-Catalyzed Enantioselective S-Alkylation of Sulfenamides with Acceptor–Acceptor Diazo Compounds Enables the Synthesis of Sulfoximines Displaying Diverse Functionality Organic Letters article journal CV OA GS

CV span

lines 142–144 · CV · published

14212. Patel, S.; Greenwood, N. S.; Mercado, B. Q.; Ellman, J. A. “Rh(II)-Catalyzed Enantioselective S-143Alkylation of Sulfenamides with Acceptor–Acceptor Diazo Compounds Enables the Synthesis of144Sulfoximines Displaying Diverse Functionality” Org. Lett. 26, 6295–6300 (2024).

Institution fields

Peer reviewed
yes
First author
Patel
Co-authors
Patel, S.; Greenwood, N. S.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(II)-Catalyzed Enantioselective S-Alkylation of Sulfenamides with Acceptor–Acceptor Diazo Compounds Enables the Synthesis of Sulfoximines Displaying Diverse FunctionalityRh(II)-Catalyzed Enantioselective S -Alkylation of Sulfenamides with Acceptor–Acceptor Diazo Compounds Enables the Synthesis of Sulfoximines Displaying Diverse FunctionalityRh (II)-catalyzed enantioselective S-alkylation of sulfenamides with acceptor-acceptor diazo compounds enables the synthesis of sulfoximines displaying diverse functionality
year cv 202420242024
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.4c0240210.1021/acs.orglett.4c02402
first author openalex PatelPatelPatel

Citations

OpenAlex
29
Scholar
28
DOI
10.1021/acs.orglett.4c02402
OpenAlex
W4400660528

Match decisions

  • doi merged · 1.00 · Run 18
2024 Synthesis of Monodehydro-Diketopiperazines Enabled by Cp*Rh(III)-Catalyzed Amine-Directed N–H Functionalization Organic Letters article journal CV OA GS

CV span

lines 132–133 · CV · published

1329. Molas, J. C.; Poag, E. M.; Ellman, J. A. “Synthesis of Monodehydro-Diketopiperazines Enabled by133Cp*Rh(III)-Catalyzed Amine-Directed N–H Functionalization” Org. Lett. 26, 8527–8531 (2024).

Institution fields

Peer reviewed
yes
First author
Molas
Co-authors
Molas, J. C.; Poag, E. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Monodehydro-Diketopiperazines Enabled by Cp*Rh(III)-Catalyzed Amine-Directed N–H FunctionalizationSynthesis of Monodehydro-Diketopiperazines Enabled by Cp*Rh(III)-Catalyzed Amine-Directed N–H Functionalization
year cv 20242024
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.4c0310510.1021/acs.orglett.4c03105
first author openalex MolasMolas

Citations

OpenAlex
3
Scholar
none
DOI
10.1021/acs.orglett.4c03105
OpenAlex
W4402906052

Match decisions

  • doi merged · 1.00 · Run 18
2024 Synthesis of N-Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One-Pot Sulfur-Arylation and Dealkylation Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 149–151 · CV · published

14914. Greenwood, N. S.; Cerny, N. P.; Deziel, A. P.; Ellman, J. A. “Synthesis of N-Acylsulfenamides150from (Hetero)Aryl Iodides and Boronic Acids by One-Pot Sulfur-Arylation and Dealkylation”151Angew. Chem. Int. Ed. 63, e202315701 (2024).

Institution fields

Peer reviewed
yes
First author
Greenwood
Co-authors
Greenwood, N. S.; Cerny, N. P.; Deziel, A. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of N-Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One-Pot Sulfur-Arylation and DealkylationSynthesis of N‐Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One‐Pot Sulfur‐Arylation and DealkylationSynthesis of N‐Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One‐Pot Sulfur‐Arylation and DealkylationSynthesis of N‐Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One‐Pot Sulfur‐Arylation and Dealkylation
year cv 2024202320232024
venue crossref Angew. Chem. Int. Ed.Angewandte ChemieAngewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20231570110.1002/ange.20231570110.1002/anie.202315701
first author openalex GreenwoodGreenwoodGreenwoodGreenwood

Also recorded as

  • W4389078065 (DOI 10.1002/ange.202315701) · same title · 2023 Synthesis of N‐Acylsulfenamides from (Hetero)Aryl Iodides and Boronic Acids by One‐Pot Sulfur‐Arylation and Dealkylation

Citations

OpenAlex
28
Scholar
27
DOI
10.1002/anie.202315701
OpenAlex
W4389078100

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2024 Synthesis of α-Quaternary Amides via Cp*Co(III)-Catalyzed Sequential C–H Bond Addition to 1,3-Dienes and Isocyanates Organic Letters article journal CV OA GS

CV span

lines 129–130 · CV · published

1298. Yeo, J.; Tassone, J. P.; Ellman, J. A. “Synthesis of α-Quaternary Amides via Cp*Co(III)-Catalyzed130Sequential C–H Bond Addition to 1,3-Dienes and Isocyanates” Org. Lett. 26, 9769–9774 (2024).

Institution fields

Peer reviewed
yes
First author
Yeo
Co-authors
Yeo, J.; Tassone, J. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of α-Quaternary Amides via Cp*Co(III)-Catalyzed Sequential C–H Bond Addition to 1,3-Dienes and IsocyanatesSynthesis of α-Quaternary Amides via Cp*Co(III)-Catalyzed Sequential C–H Bond Addition to 1,3-Dienes and Isocyanates
year cv 20242024
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.4c0374010.1021/acs.orglett.4c03740
first author openalex YeoYeo

Citations

OpenAlex
9
Scholar
none
DOI
10.1021/acs.orglett.4c03740
OpenAlex
W4403926291

Match decisions

  • doi merged · 1.00 · Run 18
2023 Imine Directed Cp*Rh(III)-Catalyzed N–H Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo Compounds Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 174–176 · CV · published

17421. Zoll, A. J.; Molas, J. C.; Mercado, B. Q.; Ellman, J. A. “Imine Directed Cp*Rh(III)-Catalyzed N–H175Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo Compounds” Angew.176Chem. Int. Ed. 62, e202210822 (2023).

Institution fields

Peer reviewed
yes
First author
Zoll
Co-authors
Zoll, A. J.; Molas, J. C.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Imine Directed Cp*Rh(III)-Catalyzed N–H Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo CompoundsImine Directed Cp*RhIII‐Catalyzed N−H Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo CompoundsImine Directed Cp*RhIII‐Catalyzed N−H Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo Compounds
year cv 202320222022
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticle
DOI crossref 10.1002/anie.20221082210.1002/anie.20221082210.1002/ange.202210822
first author openalex ZollZollZoll

Also recorded as

  • W4308327778 (DOI 10.1002/ange.202210822) · platform twin · 2022 Imine Directed Cp*RhIII‐Catalyzed N−H Functionalization and Annulation with Amino Amides, Aldehydes, and Diazo Compounds

Citations

OpenAlex
14
Scholar
none
DOI
10.1002/anie.202210822
OpenAlex
W4308188095

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2023 Preparation of Sulfilimines by Sulfur-Alkylation of N-Acyl Sulfenamides with Alkyl Halides The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 159–160 · CV · published

15917. Champlin, A. T.; Ellman, J. A. “Preparation of Sulfilimines by Sulfur-Alkylation of N-Acyl160Sulfenamides with Alkyl Halides” J. Org. Chem. 88, 7607–7614 (2023).

Institution fields

Peer reviewed
yes
First author
Champlin
Co-authors
Champlin, A. T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Preparation of Sulfilimines by Sulfur-Alkylation of N-Acyl Sulfenamides with Alkyl HalidesPreparation of Sulfilimines by Sulfur-Alkylation of N -Acyl Sulfenamides with Alkyl HalidesPreparation of sulfilimines by sulfur-alkylation of N-acyl sulfenamides with alkyl halides
year cv 202320232023
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.3c0075010.1021/acs.joc.3c00750
first author openalex ChamplinChamplinChamplin

Citations

OpenAlex
71
Scholar
68
DOI
10.1021/acs.joc.3c00750
OpenAlex
W4377938939

Match decisions

  • doi merged · 1.00 · Run 18
2023 Small Molecule PI5P4K Alpha/Beta Inhibitors and Methods of Treatment Using Same US Patent No. US 11,773,096 other CV OA GS

CV span

lines 1395–1397 · CV · published

13951. Ha, Y.; Ellman, J.; Chen, S.; Chandra-Tjin, C.; Micheli, F.’ Cianciulli, A.; Beato, C. “Small1396Molecule PI5P4K Alpha/Beta Inhibitors and Methods of Treatment Using Same” US (2023), Patent1397No. US 11,773,096.

Institution fields

Peer reviewed
none
First author
Ha
Co-authors
Ha, Y.; Ellman, J.; Chen, S.; Chandra-Tjin, C.; Micheli, F.’ Cianciulli, A.; Beato, C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Small Molecule PI5P4K Alpha/Beta Inhibitors and Methods of Treatment Using Same
year cv 2023
venue cv US Patent No. US 11,773,096
kind cv other
first author cv Ha

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2023 Stereospecific Synthesis of Unprotected, α,β-Disubstituted Tryptamines and Phenethylamines from 1,2-Disubstituted Alkenes via a One-Pot Reaction Sequence Organic Letters article journal CV OA GS

CV span

lines 162–164 · CV · published

16218. Chu, D.; Ellman, J. A. “Stereospecific Synthesis of Unprotected, α,β-Disubstituted Tryptamines and163Phenethylamines from 1,2-Disubstituted Alkenes via a One-Pot Reaction Sequence” Org. Lett. 25,1643654–3658 (2023).

Institution fields

Peer reviewed
yes
First author
Chu
Co-authors
Chu, D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Stereospecific Synthesis of Unprotected, α,β-Disubstituted Tryptamines and Phenethylamines from 1,2-Disubstituted Alkenes via a One-Pot Reaction SequenceStereospecific Synthesis of Unprotected, α,β-Disubstituted Tryptamines and Phenethylamines from 1,2-Disubstituted Alkenes via a One-Pot Reaction Sequence
year cv 20232023
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.3c0102110.1021/acs.orglett.3c01021
first author openalex ChuChu

Citations

OpenAlex
21
Scholar
none
DOI
10.1021/acs.orglett.3c01021
OpenAlex
W4376254063

Match decisions

  • doi merged · 1.00 · Run 18
2023 Sulfur-Arylation of Sulfenamides via Chan–Lam Coupling with Boronic Acids: Access to High Oxidation State Sulfur Pharmacophores Organic Letters article journal CV OA GS

CV span

lines 166–168 · CV · published

16619. Greenwood, N. S.; Ellman, J. A. “Sulfur-Arylation of Sulfenamides via Chan–Lam Coupling with167Boronic Acids: Access to High Oxidation State Sulfur Pharmacophores” Org. Lett. 25, 2830–2834168(2023).

Institution fields

Peer reviewed
yes
First author
Greenwood
Co-authors
Greenwood, N. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Sulfur-Arylation of Sulfenamides via Chan–Lam Coupling with Boronic Acids: Access to High Oxidation State Sulfur PharmacophoresSulfur-Arylation of Sulfenamides via Chan–Lam Coupling with Boronic Acids: Access to High Oxidation State Sulfur PharmacophoresSulfur-arylation of sulfenamides via Chan-Lam coupling with boronic acids: Access to high oxidation state sulfur pharmacophores
year cv 202320232023
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.3c0077910.1021/acs.orglett.3c00779
first author openalex GreenwoodGreenwoodGreenwood

Citations

OpenAlex
86
Scholar
82
DOI
10.1021/acs.orglett.3c00779
OpenAlex
W4365135691

Match decisions

  • doi merged · 1.00 · Run 18
2023 Sulfur-Arylation of Sulfenamides via Ullmann-Type Coupling with (Hetero)aryl Iodides Organic Letters article journal CV OA GS

CV span

lines 156–157 · CV · published

15616. Greenwood, N. S.; Ellman, J. A. “Sulfur-Arylation of Sulfenamides via Ullmann-Type Coupling157with (Hetero)aryl Iodides” Org. Lett. 25, 4759–4764 (2023).

Institution fields

Peer reviewed
yes
First author
Greenwood
Co-authors
Greenwood, N. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Sulfur-Arylation of Sulfenamides via Ullmann-Type Coupling with (Hetero)aryl IodidesSulfur-Arylation of Sulfenamides via Ullmann-Type Coupling with (Hetero)aryl IodidesSulfur-arylation of sulfenamides via Ullmann-type coupling with (hetero) aryl iodides
year cv 202320232023
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.3c0187410.1021/acs.orglett.3c01874
first author openalex GreenwoodGreenwoodGreenwood

Citations

OpenAlex
65
Scholar
61
DOI
10.1021/acs.orglett.3c01874
OpenAlex
W4381244777

Match decisions

  • doi merged · 1.00 · Run 18
2023 Synthesis of N-Acylsulfenamides from Amides and N-Thiosuccinimides Synthesis article journal CV OA GS

CV span

lines 170–172 · CV · published

17020. Liu, J. T.; Brandes, D. S.; Greenwood, N. S.; Ellman, J. A. “Synthesis of N-Acylsulfenamides from171Amides and N-Thiosuccinimides” Synthesis 55, 2353–2360 (2023) [Special Issue dedicated to172Prof. David A. Evans].

Institution fields

Peer reviewed
yes
First author
Liu
Co-authors
Liu, J. T.; Brandes, D. S.; Greenwood, N. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Synthesis of N-Acylsulfenamides from Amides and N-ThiosuccinimidesSynthesis of N-Acylsulfenamides from Amides and N-Thiosuccinimides
year cv 20232022
venue crossref SynthesisSynthesis
kind cv articlearticle
DOI crossref 10.1055/s-0041-173843010.1055/s-0041-1738430
first author openalex LiuLiu

Citations

OpenAlex
24
Scholar
none
DOI
10.1055/s-0041-1738430
OpenAlex
W4313455410

Match decisions

  • doi merged · 1.00 · Run 18
2023 Visible-Light-Mediated, Diastereoselective Epimerization of Exocyclic Amines Organic Letters article journal CV OA GS

CV span

lines 153–154 · CV · published

15315. Vargas-Rivera, M. A.; Ellman, J. A. “Visible-Light-Mediated, Diastereoselective Epimerization of154Exocyclic Amines” Org. Lett. 25, 9197–9201 (2023).

Institution fields

Peer reviewed
yes
First author
Vargas-Rivera
Co-authors
Vargas-Rivera, M. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Visible-Light-Mediated, Diastereoselective Epimerization of Exocyclic AminesVisible-Light-Mediated, Diastereoselective Epimerization of Exocyclic Amines
year cv 20232023
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.3c0380110.1021/acs.orglett.3c03801
first author openalex Vargas-RiveraVargas-Rivera

Citations

OpenAlex
6
Scholar
none
DOI
10.1021/acs.orglett.3c03801
OpenAlex
W4389965510

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/acscatal.2c03672 for epimerization of morpholines and piperazines.
2022 Bespoke library docking for 5-HT2A receptor agonists with antidepressant activity Nature article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Bespoke library docking for 5-HT2A receptor agonists with antidepressant activityBespoke library docking for 5-HT2A receptor agonists with antidepressant activityBespoke library docking for 5-HT2A receptor agonists with antidepressant activity
year openalex 202220242022
venue openalex NatureCarolina Digital Repository (University of North Carolina at Chapel Hill)Nature
kind openalex articlearticleother
DOI openalex 10.1038/s41586-022-05258-z10.17615/s14n-1x62
first author openalex KaplanShoichetKaplan

Also recorded as

Citations

OpenAlex
260
Scholar
286
DOI
10.1038/s41586-022-05258-z
OpenAlex
W4297497355

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: repository_copy
2022 Catalytic Enantioselective Sulfur Alkylation of Sulfenamides for the Asymmetric Synthesis of Sulfoximines Journal of the American Chemical Society article journal CV OA GS

CV span

lines 193–195 · CV · published

19325. Greenwood, N. S.; Champlin, A. T.; Ellman, J. A. “Catalytic Enantioselective Sulfur Alkylation of194Sulfenamides for the Asymmetric Synthesis of Sulfoximines” J. Am. Chem. Soc. 144, 17808–17814195(2022).

Institution fields

Peer reviewed
yes
First author
Greenwood
Co-authors
Greenwood, N. S.; Champlin, A. T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Sulfur Alkylation of Sulfenamides for the Asymmetric Synthesis of SulfoximinesCatalytic Enantioselective Sulfur Alkylation of Sulfenamides for the Asymmetric Synthesis of SulfoximinesCatalytic enantioselective sulfur alkylation of sulfenamides for the asymmetric synthesis of sulfoximines
year cv 202220222022
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.2c0915810.1021/jacs.2c09158
first author openalex GreenwoodGreenwoodGreenwood

Citations

OpenAlex
173
Scholar
161
DOI
10.1021/jacs.2c09158
OpenAlex
W4297242765

Match decisions

  • doi merged · 1.00 · Run 18
2022 C–H Bond Activation and Sequential Addition to Two Different Coupling Partners: A Versatile Approach to Molecular Complexity Chemical Society Reviews article journal CV OA GS

CV span

lines 202–204 · CV · published

20227. Brandes, D. S.; Elman, J. A. “C–H Bond Activation and Sequential Addition to Two Different203Coupling Partners: A Versatile Approach to Molecular Complexity” Chem. Soc. Rev. 51, 6738-2046756 (2022).

Institution fields

Peer reviewed
yes
First author
Brandes
Co-authors
Brandes, D. S.; Elman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv C–H Bond Activation and Sequential Addition to Two Different Coupling Partners: A Versatile Approach to Molecular ComplexityC–H bond activation and sequential addition to two different coupling partners: a versatile approach to molecular complexityC–H bond activation and sequential addition to two different coupling partners: a versatile approach to molecular complexity
year cv 202220222022
venue crossref Chem. Soc. Rev.Chemical Society ReviewsChemical Society ReviewsChemical Society Reviews
kind cv articlereviewother
DOI crossref 10.1039/d2cs00012a10.1039/d2cs00012a
first author openalex BrandesBrandesBrandes

Citations

OpenAlex
50
Scholar
44
DOI
10.1039/d2cs00012a
OpenAlex
W4285128479

Match decisions

  • doi merged · 1.00 · Run 18
2022 Defining the Structure-Activity Relationship for a Novel Class of Allosteric MKP5 Inhibitors European Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 197–200 · CV · published

19726. Gannam, Z. T. K.; Jamali, H.; Kweon, O. S.; Herrington, J.; Shillingford, S. R.; Papini, C.; Gentzel,198E.; Lolis, E.; Bennett, A. M.; Ellman, J. A.; Anderson, K. S. “Defining the Structure-Activity199Relationship for a Novel Class of Allosteric MKP5 Inhibitors” Eur. J. Med. Chem. 243, 114712200(2022).

Institution fields

Peer reviewed
yes
First author
Gannam
Co-authors
Gannam, Z. T. K.; Jamali, H.; Kweon, O. S.; Herrington, J.; Shillingford, S. R.; Papini, C.; Gentzel, E.; Lolis, E.; Bennett, A. M.; Ellman, J. A.; Anderson, K. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Defining the Structure-Activity Relationship for a Novel Class of Allosteric MKP5 InhibitorsDefining the structure-activity relationship for a novel class of allosteric MKP5 inhibitors
year cv 20222022
venue crossref Eur. J. Med. Chem.European Journal of Medicinal ChemistryEuropean Journal of Medicinal Chemistry
kind cv articlearticle
DOI crossref 10.1016/j.ejmech.2022.11471210.1016/j.ejmech.2022.114712
first author openalex GannamGannam

Citations

OpenAlex
8
Scholar
none
DOI
10.1016/j.ejmech.2022.114712
OpenAlex
W4294203325

Match decisions

  • doi merged · 1.00 · Run 18
2022 Docking a Bespoke Ultra-Large Tetrahydropyridine Library Identifies 5-HT2A Receptor Agonists Conferring New Biology Nature article journal CV OA GS

CV span

lines 182–187 · CV · published

18223. Kaplan, A. L.; Confair, D. N.; Kim. K.; Barros-Alvarez, X.; Rodriquez, R. M.; Yang, Y.; Kweon,183O. S.; Che, T.; McCorvy, J. Kamber, D. N.; Phelan, J. P.; Martins, L. C.; Pogorelov, V. M.;184DiBerto, J. F.’ Slocum, S. T.; Huang, X.-P.; Kumar, J. M.p; Robertson, M. J.; Panova, O.; Seven,185A. B.; Wetsel, W. C.; Irwin, J. J.; Skiniotis, G.; Shoichet, B. K.; Roth, B. L.; Ellman, J. A.186“Docking a Bespoke Ultra-Large Tetrahydropyridine Library Identifies 5-HT2A Receptor Agonists187Conferring New Biology” Nature 610, 582–591 (2022).

Institution fields

Peer reviewed
yes
First author
Kaplan
Co-authors
Kaplan, A. L.; Confair, D. N.; Kim. K.; Barros-Alvarez, X.; Rodriquez, R. M.; Yang, Y.; Kweon, O. S.; Che, T.; McCorvy, J.; Kamber, D. N.; Phelan, J. P.; Martins, L. C.; Pogorelov, V. M.; DiBerto, J. F.; Slocum, S. T.; Huang, X.-P.; Kumar, J. M.p; Robertson, M. J.; Panova, O.; Seven, A. B.; Wetsel, W. C.; Irwin, J. J.; Skiniotis, G.; Shoichet, B. K.; Roth, B. L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Docking a Bespoke Ultra-Large Tetrahydropyridine Library Identifies 5-HT2A Receptor Agonists Conferring New Biology
year cv 2022
venue cv Nature
kind cv article
first author cv Kaplan

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2022 Stereoselective Synthesis of Allenyl Alcohols by Cobalt(III)-Catalyzed Sequential C−H Bond Addition to 1,3-Enynes and Aldehydes Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 210–212 · CV · published

21029. Xu, C.; Tassone, J. P.; Mercado, B. Q.; Ellman, J. A. “Stereoselective Synthesis of Allenyl211Alcohols by Cobalt(III)-Catalyzed Sequential C−H Bond Addition to 1,3-Enynes and Aldehydes”212Angew. Chem. Int. Ed. 61, e202202364 (2022) [Hot Paper].

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, C.; Tassone, J. P.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Stereoselective Synthesis of Allenyl Alcohols by Cobalt(III)-Catalyzed Sequential C−H Bond Addition to 1,3-Enynes and AldehydesStereoselective Synthesis of Allenyl Alcohols by Cobalt(III)‐Catalyzed Sequential C−H Bond Addition to 1,3‐Enynes and AldehydesStereoselective Synthesis of Allenyl Alcohols by Cobalt(III)‐Catalyzed Sequential C−H Bond Addition to 1,3‐Enynes and Aldehydes
year cv 202220222022
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticle
DOI crossref 10.1002/anie.20220236410.1002/anie.20220236410.1002/ange.202202364
first author openalex XuXuXu

Also recorded as

  • W4226301486 (DOI 10.1002/ange.202202364) · same title · 2022 Stereoselective Synthesis of Allenyl Alcohols by Cobalt(III)‐Catalyzed Sequential C−H Bond Addition to 1,3‐Enynes and Aldehydes

Citations

OpenAlex
24
Scholar
none
DOI
10.1002/anie.202202364
OpenAlex
W4224077374

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2022 Tetrahydropyridine derivatives as selective agonists of 5-HT2A receptor and methods of use PCT Int. Appl. other CV OA GS

CV span

lines 1454–1456 · CV · published

14541. Ellman, J.; Confair, D.; Kweon, O. S.; Roth, B.; Kim, K.; Shoichet, B.; Levit, A.; Irwin, J. J.1455“Tetrahydropyridine derivatives as selective agonists of 5-HT2A receptor and methods of use” PCT1456Int. Appl. (2022), WO2022067165 A1 20220331.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J.; Confair, D.; Kweon, O. S.; Roth, B.; Kim, K.; Shoichet, B.; Levit, A.; Irwin, J. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Tetrahydropyridine derivatives as selective agonists of 5-HT2A receptor and methods of use
year cv 2022
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2022 Three-Component Carboformylation: α-Quaternary Aldehyde Synthesis via Co(III)-Catalysed Sequential C–H Bond Addition to Dienes and Acetic Formic Anhydride Chemical Science article journal CV OA GS

CV span

lines 178–180 · CV · published

17822. Tassone, J. P.; Yeo, J. Ellman, J. A. “Three-Component Carboformylation: α-Quaternary Aldehyde179Synthesis via Co(III)-Catalysed Sequential C–H Bond Addition to Dienes and Acetic Formic180Anhydride” Chem. Sci. 13, 14320–14326 (2022).

Institution fields

Peer reviewed
yes
First author
Tassone
Co-authors
Tassone, J. P.; Yeo, J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Three-Component Carboformylation: α-Quaternary Aldehyde Synthesis via Co(III)-Catalysed Sequential C–H Bond Addition to Dienes and Acetic Formic AnhydrideThree-component carboformylation: α-quaternary aldehyde synthesis via Co( iii )-catalysed sequential C–H bond addition to dienes and acetic formic anhydride
year cv 20222022
venue crossref Chem. Sci.Chemical ScienceChemical Science
kind cv articlearticle
DOI crossref 10.1039/d2sc05599f10.1039/d2sc05599f
first author openalex TassoneTassone

Citations

OpenAlex
11
Scholar
none
DOI
10.1039/d2sc05599f
OpenAlex
W4312112790

Match decisions

  • doi merged · 1.00 · Run 18
2022 Three-Component Friedel–Crafts Transformations: Synthesis of Alkyl and Alkenyl Trifluoromethyl Sulfides and Alkenyl Iodides Organic Letters article journal CV OA GS

CV span

lines 214–215 · CV · published

21430. Chu, D.; Ellman, J. A. “Three-Component Friedel–Crafts Transformations: Synthesis of Alkyl and215Alkenyl Trifluoromethyl Sulfides and Alkenyl Iodides” Org. Lett. 24, 2921–2925 (2022).

Institution fields

Peer reviewed
yes
First author
Chu
Co-authors
Chu, D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Three-Component Friedel–Crafts Transformations: Synthesis of Alkyl and Alkenyl Trifluoromethyl Sulfides and Alkenyl IodidesThree-Component Friedel–Crafts Transformations: Synthesis of Alkyl and Alkenyl Trifluoromethyl Sulfides and Alkenyl Iodides
year cv 20222022
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.2c0092410.1021/acs.orglett.2c00924
first author openalex ChuChu

Citations

OpenAlex
11
Scholar
none
DOI
10.1021/acs.orglett.2c00924
OpenAlex
W4223411289

Match decisions

  • doi merged · 1.00 · Run 18
2022 Visible Light-Mediated, Highly Diastereoselective Epimerization of Lactams from the Most Accessible to the More Stable Stereoisomer ACS Catalysis article journal CV OA GS

CV span

lines 206–208 · CV · published

20628. Kazerouni, A. M.; Brandes, D. S.; Davies, C. C.; Cotter, L. F.; Mayer, J. M.; Chen, S.; Ellman, J. A.207“Visible Light-Mediated, Highly Diastereoselective Epimerization of Lactams from the Most208Accessible to the More Stable Stereoisomer” ACS Catal. 12, 7798–7803 (2022).

Institution fields

Peer reviewed
yes
First author
Kazerouni
Co-authors
Kazerouni, A. M.; Brandes, D. S.; Davies, C. C.; Cotter, L. F.; Mayer, J. M.; Chen, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Visible Light-Mediated, Highly Diastereoselective Epimerization of Lactams from the Most Accessible to the More Stable StereoisomerVisible Light-Mediated, Highly Diastereoselective Epimerization of Lactams from the Most Accessible to the More Stable Stereoisomer
year cv 20222022
venue crossref ACS Catal.ACS CatalysisACS Catalysis
kind cv articlearticle
DOI crossref 10.1021/acscatal.2c0223210.1021/acscatal.2c02232
first author openalex KazerouniKazerouni

Citations

OpenAlex
21
Scholar
none
DOI
10.1021/acscatal.2c02232
OpenAlex
W4283013426

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/acscatal.2c03672 for epimerization of morpholines and piperazines.
2022 Visible Light-Mediated, Highly Stereoselective Epimerization of Morpholines and Piperazines to the More Stable Isomers ACS Catalysis article journal CV OA GS

CV span

lines 189–191 · CV · published

18924. Shen, Z.; Vargas-Rivera, M.; Rigby, E. L.; Chen, S.; Ellman, J. A. “Visible Light-Mediated, Highly190Stereoselective Epimerization of Morpholines and Piperazines to the More Stable Isomers” ACS191Catal. 12, 12860–12868 (2022).

Institution fields

Peer reviewed
yes
First author
Shen
Co-authors
Shen, Z.; Vargas-Rivera, M.; Rigby, E. L.; Chen, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Visible Light-Mediated, Highly Stereoselective Epimerization of Morpholines and Piperazines to the More Stable IsomersVisible Light-Mediated, Diastereoselective Epimerization of Morpholines and Piperazines to More Stable Isomers
year cv 20222022
venue crossref ACS Catal.ACS CatalysisACS Catalysis
kind cv articlearticle
DOI crossref 10.1021/acscatal.2c0367210.1021/acscatal.2c03672
first author openalex ShenShen

Citations

OpenAlex
17
Scholar
none
DOI
10.1021/acscatal.2c03672
OpenAlex
W4304014637

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/acscatal.2c03672 for epimerization of morpholines and piperazines.
2021 General Light-Mediated, Highly Diastereoselective Piperidine Epimerization: From Most Accessible to Most Stable Stereoisomer Journal of the American Chemical Society article journal CV OA GS

CV span

lines 233–235 · CV · published

23335. Shen, Z.; Walker, M. M.; Chen, S.; Parada, G. A.; Chu, D. M.; Dongbang, S.; Mayer, J. M.; Houk,234K. N.; Ellman, J. A. “General Light-Mediated, Highly Diastereoselective Piperidine Epimerization:235From Most Accessible to Most Stable Stereoisomer” J. Am. Chem. Soc. 143, 126-131 (2021).

Institution fields

Peer reviewed
yes
First author
Shen
Co-authors
Shen, Z.; Walker, M. M.; Chen, S.; Parada, G. A.; Chu, D. M.; Dongbang, S.; Mayer, J. M.; Houk, K. N.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General Light-Mediated, Highly Diastereoselective Piperidine Epimerization: From Most Accessible to Most Stable StereoisomerGeneral Light-Mediated, Highly Diastereoselective Piperidine Epimerization: From Most Accessible to Most Stable StereoisomerGeneral light-mediated, highly diastereoselective piperidine epimerization: from most accessible to most stable stereoisomer
year cv 202120202021
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.0c1191110.1021/jacs.0c11911
first author openalex ShenShenShen

Citations

OpenAlex
42
Scholar
48
DOI
10.1021/jacs.0c11911
OpenAlex
W3113667217

Match decisions

  • doi merged · 1.00 · Run 18
2021 Pharmacological Inhibition of PI5P4Kα/β Disrupts Cell Energy Metabolism and Selectively Kills p53-Null Tumor Cells Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 221–223 · CV · published

22132. Chen, S.; Chandra Tjin, C.; Gao, X.; Xue, Y.; Jiao, H.; Zhang, R.; Wu, M.; He, Z.; Ellman, J. A.;222Ha, Y. Pharmacological Inhibition of PI5P4Kα/β Disrupts Cell Energy Metabolism and Selectively223Kills p53-Null Tumor Cells. Proc. Natl. Acad. Sci. USA 118, e2002486118 (2021).

Institution fields

Peer reviewed
yes
First author
Chen
Co-authors
Chen, S.; Chandra Tjin, C.; Gao, X.; Xue, Y.; Jiao, H.; Zhang, R.; Wu, M.; He, Z.; Ellman, J. A.; Ha, Y.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Pharmacological Inhibition of PI5P4Kα/β Disrupts Cell Energy Metabolism and Selectively Kills p53-Null Tumor CellsPharmacological inhibition of PI5P4Kα/β disrupts cell energy metabolism and selectively kills p53-null tumor cellsPharmacological inhibition of PI5P4Kα/β disrupts cell energy metabolism and selectively kills p53-null tumor cells
year cv 202120212021
venue crossref Proc. Natl. Acad. Sci. USAProceedings of the National Academy of SciencesProceedings of the National Academy of SciencesProceedings of the National Academy of Sciences
kind cv articlearticleother
DOI crossref 10.1073/pnas.200248611810.1073/pnas.2002486118
first author openalex ChenChenChen

Citations

OpenAlex
31
Scholar
46
DOI
10.1073/pnas.2002486118
OpenAlex
W3162907812

Match decisions

  • doi merged · 1.00 · Run 18
2021 Rhodium-Catalyzed C–H Alkenylation/Electro-cyclization Cascade Provides Dihydropyridines That Serve as Versatile Intermediates to Diverse Nitrogen Heterocycles Accounts of Chemical Research article journal CV OA GS

CV span

lines 229–231 · CV · published

22934. Dongbang, S.; Confair, D. N.; Ellman, J. A. “Rhodium-Catalyzed C–H Alkenylation/Electro-230cyclization Cascade Provides Dihydropyridines That Serve as Versatile Intermediates to Diverse231Nitrogen Heterocycles” Acc. Chem. Res. 54, 1766-1778 (2021).

Institution fields

Peer reviewed
yes
First author
Dongbang
Co-authors
Dongbang, S.; Confair, D. N.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed C–H Alkenylation/Electro-cyclization Cascade Provides Dihydropyridines That Serve as Versatile Intermediates to Diverse Nitrogen HeterocyclesRhodium-Catalyzed C–H Alkenylation/Electrocyclization Cascade Provides Dihydropyridines That Serve as Versatile Intermediates to Diverse Nitrogen HeterocyclesRhodium-catalyzed C–H alkenylation/electrocyclization cascade provides dihydropyridines that serve as versatile intermediates to diverse nitrogen heterocycles
year cv 202120212021
venue crossref Acc. Chem. Res.Accounts of Chemical ResearchAccounts of chemical researchAccounts of Chemical Research
kind cv articlearticleother
DOI crossref 10.1021/acs.accounts.1c0002710.1021/acs.accounts.1c00027
first author openalex DongbangDongbangDongbang

Citations

OpenAlex
85
Scholar
84
DOI
10.1021/acs.accounts.1c00027
OpenAlex
W3138387142

Match decisions

  • doi merged · 1.00 · Run 18
2021 Synthesis of Nitrile Bearing Acyclic Quaternary Centers via Co(III)‐Catalyzed Sequential C–H Bond Addition to Dienes and N‐Cyanosuccinimide Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 237–239 · CV · published

23736. Dongbang, S.; Ellman, Jonathan A. “Synthesis of Nitrile Bearing Acyclic Quaternary Centers via238Co(III)‐Catalyzed Sequential C–H Bond Addition to Dienes and N‐Cyanosuccinimide” Angew.239Chem. Int. Ed. 60, 2135-2139 (2021).

Institution fields

Peer reviewed
yes
First author
Dongbang
Co-authors
Dongbang, S.; Ellman, Jonathan A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Nitrile Bearing Acyclic Quaternary Centers via Co(III)‐Catalyzed Sequential C–H Bond Addition to Dienes and N‐CyanosuccinimideSynthesis of Nitrile Bearing Acyclic Quaternary Centers through Co(III)‐Catalyzed Sequential C−H Bond Addition to Dienes and N‐CyanosuccinimideSynthesis of Nitrile Bearing Acyclic Quaternary Centers through Co(III)‐Catalyzed Sequential C−H Bond Addition to Dienes and N‐CyanosuccinimideSynthesis of Nitrile Bearing Acyclic Quaternary Centers through Co(III)‐Catalyzed Sequential C−H Bond Addition to Dienes and N‐Cyanosuccinimide
year cv 2021202020202021
venue crossref Angew. Chem. Int. Ed.Angewandte ChemieAngewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20201073510.1002/ange.20201073510.1002/anie.202010735
first author openalex DongbangDongbangDongbangDongbang

Also recorded as

  • W3090078198 (DOI 10.1002/ange.202010735) · platform twin · 2020 Synthesis of Nitrile Bearing Acyclic Quaternary Centers through Co(III)‐Catalyzed Sequential C−H Bond Addition to Dienes and N‐Cyanosuccinimide

Citations

OpenAlex
33
Scholar
32
DOI
10.1002/anie.202010735
OpenAlex
W4210377385

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2021 Synthesis of α-Branched Amines by Three- and Four-Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing Group Organic Letters article journal CV OA GS

CV span

lines 217–219 · CV · published

21731. Brandes, D. S.; Muma, A. S.; Elman, J. A. “Synthesis of α-Branched Amines by Three- and Four-218Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing219Group” Org. Lett. 23, 9597-9601 (2021).

Institution fields

Peer reviewed
yes
First author
Brandes
Co-authors
Brandes, D. S.; Muma, A. S.; Elman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of α-Branched Amines by Three- and Four-Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing GroupSynthesis of α-Branched Amines by Three- and Four-Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing Group
year cv 20212021
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.1c0380710.1021/acs.orglett.1c03807
first author openalex BrandesBrandes

Citations

OpenAlex
21
Scholar
none
DOI
10.1021/acs.orglett.1c03807
OpenAlex
W4200360493

Match decisions

  • doi merged · 1.00 · Run 18
2021 Three-Component 1,2-Carboamidation of Bridged Bicyclic Alkenes via RhIII-Catalyzed Addition of C–H Bonds and Amidating Reagents Organic Letters article journal CV OA GS

CV span

lines 225–227 · CV · published

22533. Brandes, D. S.; Sirvent, A.; Mercado, B. Q.; Ellman, J. A. “Three-Component 1,2-Carboamidation226of Bridged Bicyclic Alkenes via RhIII-Catalyzed Addition of C–H Bonds and Amidating Reagents”227Org. Lett. 23, 2836–2840 (2021).

Institution fields

Peer reviewed
yes
First author
Brandes
Co-authors
Brandes, D. S.; Sirvent, A.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Three-Component 1,2-Carboamidation of Bridged Bicyclic Alkenes via RhIII-Catalyzed Addition of C–H Bonds and Amidating ReagentsThree-Component 1,2-Carboamidation of Bridged Bicyclic Alkenes via RhIII-Catalyzed Addition of C–H Bonds and Amidating ReagentsThree-component 1, 2-carboamidation of bridged bicyclic alkenes via RhIII-catalyzed addition of C–H bonds and amidating reagents
year cv 202120212021
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.1c0085110.1021/acs.orglett.1c00851
first author openalex BrandesBrandesBrandes

Citations

OpenAlex
57
Scholar
54
DOI
10.1021/acs.orglett.1c00851
OpenAlex
W3136089033

Match decisions

  • doi merged · 1.00 · Run 18
2020 An allosteric site on MKP5 reveals a strategy for small molecule inhibition Science Signaling article journal CV OA GS

CV span

lines 244–247 · CV · published

24438. Gannam, Z. T. K.; Min, K.; Shillingford, S. R.; Zhang, L.; Herrington, J.; Abriola, L.; Gareiss, P.245C.; Pantouris, G.; Tzouvelekis, A.; Kaminski, N.; Zhang, X.; Yu, J.; Jamali, H.; Ellman, J. A.;246Lolis, E.; Anderson, K. S.; Bennett, A. M. “An allosteric site on MKP5 reveals a strategy for small247molecule inhibition” Science Signaling 13, eaba3043 (2020).

Institution fields

Peer reviewed
yes
First author
Gannam
Co-authors
Gannam, Z. T. K.; Min, K.; Shillingford, S. R.; Zhang, L.; Herrington, J.; Abriola, L.; Gareiss, P. C.; Pantouris, G.; Tzouvelekis, A.; Kaminski, N.; Zhang, X.; Yu, J.; Jamali, H.; Ellman, J. A.; Lolis, E.; Anderson, K. S.; Bennett, A. M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv An allosteric site on MKP5 reveals a strategy for small molecule inhibitionAn allosteric site on MKP5 reveals a strategy for small-molecule inhibition
year cv 20202020
venue crossref Science SignalingScience Signaling
kind cv articlearticle
DOI crossref 10.1126/scisignal.aba304310.1126/scisignal.aba3043
first author openalex GannamGannam

Citations

OpenAlex
22
Scholar
none
DOI
10.1126/scisignal.aba3043
OpenAlex
W3081426032

Match decisions

  • doi merged · 1.00 · Run 18
2020 Annulation of Hydrazones and Alkynes via Rhodium(III)-Catalyzed Dual C–H Activation: Synthesis of Pyrrolopyridazines and Azolopyridazines Organic Letters article journal CV OA GS

CV span

lines 253–255 · CV · published

25340. Streit, A. D.; Zoll, A. J.; Hoang, G. L.; Ellman, J. A. “Annulation of Hydrazones and Alkynes via254Rhodium(III)-Catalyzed Dual C–H Activation: Synthesis of Pyrrolopyridazines and255Azolopyridazines” Org. Lett. 22, 1217-122 (2020).

Institution fields

Peer reviewed
yes
First author
Streit
Co-authors
Streit, A. D.; Zoll, A. J.; Hoang, G. L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Annulation of Hydrazones and Alkynes via Rhodium(III)-Catalyzed Dual C–H Activation: Synthesis of Pyrrolopyridazines and AzolopyridazinesAnnulation of Hydrazones and Alkynes via Rhodium(III)-Catalyzed Dual C–H Activation: Synthesis of Pyrrolopyridazines and AzolopyridazinesAnnulation of Hydrazones and Alkynes via Rhodium (III)-Catalyzed Dual C–H Activation: Synthesis of Pyrrolopyridazines and Azolopyridazines
year cv 202020202020
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.0c0018610.1021/acs.orglett.0c00186
first author openalex StreitStreitStreit

Citations

OpenAlex
18
Scholar
28
DOI
10.1021/acs.orglett.0c00186
OpenAlex
W3003031689

Match decisions

  • doi merged · 1.00 · Run 18
2020 Cobalt(III)-Catalyzed Diastereoselective Three-Component C–H Bond Addition to Butadiene and Activated Ketones Synthesis article journal CV OA GS

CV span

lines 261–263 · CV · published

26142. Shen, Z.; Li, C.; Mercado, B. Q.; Ellman, J. A. “Cobalt(III)-Catalyzed Diastereoselective Three-262Component C–H Bond Addition to Butadiene and Activated Ketones” Synthesis 51, 1239-1246263(2020) [Domino C–H functionalization reaction/cascade catalysis in honor of Prof. Mark Lautens].

Institution fields

Peer reviewed
yes
First author
Shen
Co-authors
Shen, Z.; Li, C.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Cobalt(III)-Catalyzed Diastereoselective Three-Component C–H Bond Addition to Butadiene and Activated KetonesCobalt(III)-Catalyzed Diastereoselective Three-Component C–H Bond Addition to Butadiene and Activated Ketones
year cv 20202019
venue crossref SynthesisSynthesis
kind cv articlearticle
DOI crossref 10.1055/s-0039-169074110.1055/s-0039-1690741
first author openalex ShenShen

Citations

OpenAlex
17
Scholar
none
DOI
10.1055/s-0039-1690741
OpenAlex
W2984500983

Match decisions

  • doi merged · 1.00 · Run 18
2020 Co(III)-Catalyzed C-H Amidation of Dehydroalanine for the Site-Selective Structural Diversification of Thiostrepton Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 257–259 · CV · published

25741. Scamp, R. J.; deRamon, E.; Paulson, E. K.; Miller, S. J.; Ellman, J. A. “Co(III)-Catalyzed C-H258Amidation of Dehydroalanine for the Site-Selective Structural Diversification of Thiostrepton”259Angew. Chem. Int. Ed. 59, 890-895 (2020).

Institution fields

Peer reviewed
yes
First author
Scamp
Co-authors
Scamp, R. J.; deRamon, E.; Paulson, E. K.; Miller, S. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Co(III)-Catalyzed C-H Amidation of Dehydroalanine for the Site-Selective Structural Diversification of ThiostreptonCobalt(III)‐Catalyzed C−H Amidation of Dehydroalanine for the Site‐Selective Structural Diversification of ThiostreptonCobalt(III)‐Catalyzed C−H Amidation of Dehydroalanine for the Site‐Selective Structural Diversification of ThiostreptonCobalt (III)‐Catalyzed C− H Amidation of Dehydroalanine for the Site‐Selective Structural Diversification of Thiostrepton
year cv 2020201920192020
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20191188610.1002/anie.20191188610.1002/ange.201911886
first author openalex ScampScampScampScamp

Also recorded as

  • W4230010054 (DOI 10.1002/ange.201911886) · platform twin · 2019 Cobalt(III)‐Catalyzed C−H Amidation of Dehydroalanine for the Site‐Selective Structural Diversification of Thiostrepton

Citations

OpenAlex
61
Scholar
66
DOI
10.1002/anie.201911886
OpenAlex
W2991312126

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2020 Highly Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed C–H Arylation and Epimerization Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 249–251 · CV · published

24939. Walker, M. M.; Koronkiewicz, B.; Chen, S.; Houk, K. N.; Mayer, J. M.; Ellman, J. A. “Highly250Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed C–H Arylation and251Epimerization” J. Am. Chem. Soc. 142, 8194-8202 (2020).

Institution fields

Peer reviewed
yes
First author
Walker
Co-authors
Walker, M. M.; Koronkiewicz, B.; Chen, S.; Houk, K. N.; Mayer, J. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed C–H Arylation and EpimerizationHighly Diastereoselective Functionalization of Piperidines by Photoredox-Catalyzed α-Amino C–H Arylation and EpimerizationHighly Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed C–H Arylation and EpimerizationHighly Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed C–H Arylation and EpimerizationHighly Diastereoselective Functionalization of Piperidines by Photoredox Catalyzed α-Amino C–H Arylation and Epimerization
year cv 20202020201920192020
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemRxivChemRxivJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleworking_paperworking_paperother
DOI crossref 10.1021/jacs.9b1316510.1021/jacs.9b1316510.26434/chemrxiv.1133664210.26434/chemrxiv.11336642.v1
preprint DOI openalex 10.26434/chemrxiv.1133664210.26434/chemrxiv.11336642.v1
first author openalex WalkerWalkerWalkerWalkerWalker

Also recorded as

Citations

OpenAlex
84
Scholar
90
DOI
10.1021/jacs.9b13165
OpenAlex
W3016088152

Match decisions

  • passthrough_guard not merged · 1.00 · same_source · Run 18 Records share the DOI 10.1021/jacs.9b13165 for highly diastereoselective functionalization of piperidines.
  • doi merged · 1.00 · Run 18
2020 Preparation of 2-amino-dihydropteridinones as PI5P4K α/β inhibitors for the treatment of metabolic diseases such as diabetes, obesity and cancer PCT Int. Appl. other CV OA GS

CV span

lines 1461–1463 · CV · published

14613. Ha, Y.; Ellman, J.; Chen, S.; Tjin, C. C.; Micheli, F.; Cianciulli, A.; Beato, C. “Preparation of 2-1462amino-dihydropteridinones as PI5P4K α/β inhibitors for the treatment of metabolic diseases such as1463diabetes, obesity and cancer” PCT Int. Appl. (2020), WO 2020033823 A1 20200213.

Institution fields

Peer reviewed
none
First author
Ha
Co-authors
Ha, Y.; Ellman, J.; Chen, S.; Tjin, C. C.; Micheli, F.; Cianciulli, A.; Beato, C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of 2-amino-dihydropteridinones as PI5P4K α/β inhibitors for the treatment of metabolic diseases such as diabetes, obesity and cancer
year cv 2020
venue cv PCT Int. Appl.
kind cv other
first author cv Ha

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2020 Rh(III)-Catalyzed Imidoyl C–H Carbamylation and Cyclization to Bicyclic [1,3,5]Triazinones Organic Letters article journal CV OA GS

CV span

lines 241–242 · CV · published

24137. Confair, D. N.; Greenwood, N. S.; Mercado, B. Q.; Ellman, J. A. “Rh(III)-Catalyzed Imidoyl C–H242Carbamylation and Cyclization to Bicyclic [1,3,5]Triazinones” Org. Lett. 22, 8993–8997 (2020).

Institution fields

Peer reviewed
yes
First author
Confair
Co-authors
Confair, D. N.; Greenwood, N. S.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed Imidoyl C–H Carbamylation and Cyclization to Bicyclic [1,3,5]TriazinonesRh(III)-Catalyzed Imidoyl C–H Carbamylation and Cyclization to Bicyclic [1,3,5]Triazinones
year cv 20202020
venue crossref Org. Lett.Organic LettersOrganic Letters
kind cv articlearticle
DOI crossref 10.1021/acs.orglett.0c0339310.1021/acs.orglett.0c03393
first author openalex ConfairConfair

Citations

OpenAlex
11
Scholar
none
DOI
10.1021/acs.orglett.0c03393
OpenAlex
W3103005986

Match decisions

  • doi merged · 1.00 · Run 18
2020 Thiostrepton analogs and methods of making and using same PCT Int. Appl. other CV OA GS

CV span

lines 1458–1459 · CV · published

14582. Ellman, J.; Scamp, R.; Miller, S. J.; De Ramon, E. “Thiostrepton analogs and methods of making1459and using same” PCT Int. Appl. (2020), WO 2020232048 A1 20201119.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J.; Scamp, R.; Miller, S. J.; De Ramon, E.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Thiostrepton analogs and methods of making and using same
year cv 2020
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2019 Asymmetric Synthesis of (−)-Naltrexone Chemical Science article journal CV OA GS

CV span

lines 282–283 · CV · published

28248. Dongbang, S.; Pedersen, B.; Ellman, J. A. “Asymmetric Synthesis of (−)-Naltrexone” Chem.283Sci. 10, 535–541 (2019).

Institution fields

Peer reviewed
yes
First author
Dongbang
Co-authors
Dongbang, S.; Pedersen, B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of (−)-NaltrexoneAsymmetric synthesis of (−)-naltrexone
year cv 20192018
venue crossref Chem. Sci.Chemical ScienceChemical Science
kind cv articlearticle
DOI crossref 10.1039/c8sc03748e10.1039/c8sc03748e
first author openalex DongbangDongbang

Citations

OpenAlex
24
Scholar
none
DOI
10.1039/c8sc03748e
OpenAlex
W2896916499

Match decisions

  • doi merged · 1.00 · Run 18
2019 Dihydrothieno[3,4-h] quinazoline and related compounds and compositions for treating fibrosis PCT Int. Appl. other CV OA GS

CV span

lines 1465–1467 · CV · published

14654. Bennett, A.; Ellman, J.; Jamali, H.; Anderson, K. S.; Lolis, E.; Hoyer, D. “Dihydrothieno[3,4-h]1466quinazoline and related compounds and compositions for treating fibrosis” PCT Int. Appl. (2019),1467WO 2019126141 A1 20190627.

Institution fields

Peer reviewed
none
First author
Bennett
Co-authors
Bennett, A.; Ellman, J.; Jamali, H.; Anderson, K. S.; Lolis, E.; Hoyer, D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Dihydrothieno[3,4-h] quinazoline and related compounds and compositions for treating fibrosis
year cv 2019
venue cv PCT Int. Appl.
kind cv other
first author cv Bennett

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2019 Synthesis of Homoallylic Alcohols with Acyclic Quaternary Centers via CoIII‐Catalyzed Three‐Component C–H Bond Addition to Internally Substituted Dienes and Carbonyls Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 271–273 · CV · published

27145. Dongbang, S.; Shen, Z.; Ellman, J. A. “Synthesis of Homoallylic Alcohols with Acyclic Quaternary272Centers via CoIII‐Catalyzed Three‐Component C–H Bond Addition to Internally Substituted273Dienes and Carbonyls” Angew. Chem. Int. Ed. 58, 12590–12594 (2019).

Institution fields

Peer reviewed
yes
First author
Dongbang
Co-authors
Dongbang, S.; Shen, Z.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Homoallylic Alcohols with Acyclic Quaternary Centers via CoIII‐Catalyzed Three‐Component C–H Bond Addition to Internally Substituted Dienes and CarbonylsSynthesis of Homoallylic Alcohols with Acyclic Quaternary Centers through CoIII‐Catalyzed Three‐Component C−H Bond Addition to Internally Substituted Dienes and CarbonylsSynthesis of Homoallylic Alcohols with Acyclic Quaternary Centers through CoIII‐Catalyzed Three‐Component C−H Bond Addition to Internally Substituted Dienes and CarbonylsSynthesis of Homoallylic Alcohols with Acyclic Quaternary Centers through CoIII‐Catalyzed Three‐Component C−H Bond Addition to Internally Substituted Dienes …
year cv 2019201920192019
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20190663310.1002/anie.20190663310.1002/ange.201906633
first author openalex DongbangDongbangDongbangDongbang

Also recorded as

  • W4247271842 (DOI 10.1002/ange.201906633) · platform twin · 2019 Synthesis of Homoallylic Alcohols with Acyclic Quaternary Centers through CoIII‐Catalyzed Three‐Component C−H Bond Addition to Internally Substituted Dienes and Carbonyls

Citations

OpenAlex
51
Scholar
53
DOI
10.1002/anie.201906633
OpenAlex
W2962337637

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2019 The Breadth and Depth of C–H Functionalization The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 265–266 · CV · published

26543. Ellman, J. A.; Ackermann, L.; Shi, B.-F. “The Breadth and Depth of C–H Functionalization” J.266Org. Chem. 84, 12701-12704 (2019).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J. A.; Ackermann, L.; Shi, B.-F.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Breadth and Depth of C–H FunctionalizationThe Breadth and Depth of C–H Functionalization
year cv 20192019
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/acs.joc.9b0266310.1021/acs.joc.9b02663
first author openalex EllmanEllman

Citations

OpenAlex
21
Scholar
none
DOI
10.1021/acs.joc.9b02663
OpenAlex
W2981247921

Match decisions

  • passthrough_guard not merged · 1.00 · same_source · Run 18 Records share the DOI 10.1021/jacs.9b13165 for highly diastereoselective functionalization of piperidines.
  • doi merged · 1.00 · Run 18
2019 Three-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrido[1,2-a]pyrimidin-4-ones Organic Letters article journal CV OA GS

CV span

lines 275–277 · CV · published

27546. Hoang, G. L.; Zoll, A. J.; Ellman, J. A. “Three-Component Coupling of Aldehydes, 2-276Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis277of Pyrido[1,2-a]pyrimidin-4-ones” Org. Lett. 21, 3886-3890 (2019).

Institution fields

Peer reviewed
yes
First author
Hoang
Co-authors
Hoang, G. L.; Zoll, A. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Three-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrido[1,2-a]pyrimidin-4-onesThree-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrido[1,2-a]pyrimidin-4-onesThree-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium (III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrido [1, 2-a] pyrimidin-4-ones
year cv 201920192019
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.9b0077910.1021/acs.orglett.9b00779
first author openalex HoangHoangHoang

Citations

OpenAlex
40
Scholar
42
DOI
10.1021/acs.orglett.9b00779
OpenAlex
W2924218133

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/acs.joc.8b02606 for the pyrazolopyrimidines paper.
2019 α-Branched Amines by Catalytic 1,1-Addition of C–H Bonds and Aminating Agents to Terminal Alkenes Nature Catalysis article journal CV OA GS

CV span

lines 268–269 · CV · published

26844. Maity, S.; Potter, T. J.; Ellman, J. A. “α-Branched Amines by Catalytic 1,1-Addition of C–H Bonds269and Aminating Agents to Terminal Alkenes” Nat. Catal. 2, 756–762 (2019).

Institution fields

Peer reviewed
yes
First author
Maity
Co-authors
Maity, S.; Potter, T. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv α-Branched Amines by Catalytic 1,1-Addition of C–H Bonds and Aminating Agents to Terminal Alkenesα-Branched amines by catalytic 1,1-addition of C–H bonds and aminating agents to terminal alkenesα-Branched amines by catalytic 1, 1-addition of C–H bonds and aminating agents to terminal alkenes
year cv 201920192019
venue crossref Nat. Catal.Nature CatalysisNature catalysisNature Catalysis
kind cv articlearticleother
DOI crossref 10.1038/s41929-019-0330-710.1038/s41929-019-0330-7
first author openalex MaityMaityMaity

Citations

OpenAlex
133
Scholar
124
DOI
10.1038/s41929-019-0330-7
OpenAlex
W2967011448

Match decisions

  • doi merged · 1.00 · Run 18
2019 π-Facial Selectivities in Hydride Reductions of Hindered Endocyclic Iminium Ions The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 279–280 · CV · published

27947. Chen, S.; Chan, A. Y.; Walker, M. M.; Ellman, J. A.; Houk, K. N. “π-Facial Selectivities in280Hydride Reductions of Hindered Endocyclic Iminium Ions” J. Org. Chem. 84, 273–281 (2019).

Institution fields

Peer reviewed
yes
First author
Chen
Co-authors
Chen, S.; Chan, A. Y.; Walker, M. M.; Ellman, J. A.; Houk, K. N.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv π-Facial Selectivities in Hydride Reductions of Hindered Endocyclic Iminium Ionsπ-Facial Selectivities in Hydride Reductions of Hindered Endocyclic Iminium Ions
year cv 20192018
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/acs.joc.8b0260310.1021/acs.joc.8b02603
first author openalex ChenChen

Citations

OpenAlex
4
Scholar
none
DOI
10.1021/acs.joc.8b02603
OpenAlex
W2902030503

Match decisions

  • doi merged · 1.00 · Run 18
2018 Formation of Aminocyclopentadienes from Silyldihydropyridines: Ring Contractions Driven by Anion Stabilization Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 305–307 · CV · published

30554. Walker, M. M.; Chen, S.; Houk, K.; Ellman, J. A. “Formation of Aminocyclopentadienes from306Silyldihydropyridines: Ring Contractions Driven by Anion Stabilization” Angew. Chem. Int. Ed.30757, 6605-6609 (2018).

Institution fields

Peer reviewed
yes
First author
Walker
Co-authors
Walker, M. M.; Chen, S.; Houk, K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Formation of Aminocyclopentadienes from Silyldihydropyridines: Ring Contractions Driven by Anion StabilizationFormation of Aminocyclopentadienes from Silyldihydropyridines: Ring Contractions Driven by Anion StabilizationFormation of Aminocyclopentadienes from Silyldihydropyridines: Ring Contractions Driven by Anion Stabilization
year cv 201820182018
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticle
DOI crossref 10.1002/anie.20180059610.1002/anie.20180059610.1002/ange.201800596
first author openalex WalkerWalkerWalker

Also recorded as

Citations

OpenAlex
4
Scholar
none
DOI
10.1002/anie.201800596
OpenAlex
W2792473073

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2018 Inhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia models Mol. Psychiatry article journal CV OA GS

CV span

lines 313–317 · CV · published

31356. Xu, J.; Hartley, B. J.; Kurup, P.; Phillips, A.; Topol, A.; Xu, M.; Ononenyi, C.; Foscue, E.; Ho, S-314M.; Baguley, T. D.; Carty, N.; Barros, C. S.; Muller, U.; Gupta, S.; Gochman, P.; Rapoport, J.;315Ellman, J. A.; Pittenger, C.; Aronow, B.; Nairn, A. C.; Nestor, M. W.; Lombroso, P. J.; Brennand,316K. J. “Inhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia models”317Mol. Psychiatry 23, 271–281 (2018).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, J.; Hartley, B. J.; Kurup, P.; Phillips, A.; Topol, A.; Xu, M.; Ononenyi, C.; Foscue, E.; Ho, S-M.; Baguley, T. D.; Carty, N.; Barros, C. S.; Muller, U.; Gupta, S.; Gochman, P.; Rapoport, J.; Ellman, J. A.; Pittenger, C.; Aronow, B.; Nairn, A. C.; Nestor, M. W.; Lombroso, P. J.; Brennand, K. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Inhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia modelsInhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia modelsInhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia models
year cv 201820162018
venue cv Mol. PsychiatryMolecular PsychiatryMolecular psychiatry
kind cv articlearticleother
DOI openalex 10.1038/mp.2016.163
first author cv XuXuXu

Also recorded as

Citations

OpenAlex
41
Scholar
51
DOI
10.1038/mp.2016.163

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2018 Rh(III)-Catalyzed Synthesis of Isoquinolones and 2-Pyridones via Annulation of N-Methoxyamides and Nitroalkenes European Journal of Organic Chemistry article journal CV OA GS

CV span

lines 301–303 · CV · published

30153. Potter, T. J.; Li, Y.; Ward, M. D.; Ellman, J. A. “Rh(III)-Catalyzed Synthesis of Isoquinolones and3022-Pyridones via Annulation of N-Methoxyamides and Nitroalkenes” Eur. J. Org. Chem. 4381–4388303(2018) [International Adivsory Board 20th Anniversary Issue].

Institution fields

Peer reviewed
yes
First author
Potter
Co-authors
Potter, T. J.; Li, Y.; Ward, M. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed Synthesis of Isoquinolones and 2-Pyridones via Annulation of N-Methoxyamides and NitroalkenesRhIII‐Catalyzed Synthesis of Isoquinolones and 2‐Pyridones by Annulation of N‐Methoxyamides and NitroalkenesRhIII‐Catalyzed Synthesis of Isoquinolones and 2‐Pyridones by Annulation of N‐Methoxyamides and Nitroalkenes
year cv 201820182018
venue crossref Eur. J. Org. Chem.European Journal of Organic ChemistryEuropean Journal of Organic ChemistryEuropean Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1002/ejoc.20180074510.1002/ejoc.201800745
first author openalex PotterPotterPotter

Citations

OpenAlex
29
Scholar
29
DOI
10.1002/ejoc.201800745
OpenAlex
W2808364894

Match decisions

  • doi merged · 1.00 · Run 18
2018 Rhodium(III)-Catalyzed C–H Functionalization of C-Alkenyl Azoles with Sulfoxonium Ylides for the Synthesis of Bridgehead N-Fused [5,6]-bicyclic Heterocycles Tetrahedron article journal CV OA GS

CV span

lines 319–321 · CV · published

31957. Hoang, G. L.; Ellman, J. A. “Rhodium(III)-Catalyzed C–H Functionalization of C-Alkenyl Azoles320with Sulfoxonium Ylides for the Synthesis of Bridgehead N-Fused [5,6]-bicyclic Heterocycles”321Tetrahedron 74, 3318-3324 (2018) [Herzon Tetrahedron Award Issue].

Institution fields

Peer reviewed
yes
First author
Hoang
Co-authors
Hoang, G. L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Rhodium(III)-Catalyzed C–H Functionalization of C-Alkenyl Azoles with Sulfoxonium Ylides for the Synthesis of Bridgehead N-Fused [5,6]-bicyclic HeterocyclesRhodium(III)-catalyzed C–H functionalization of C-alkenyl azoles with sulfoxonium ylides for the synthesis of bridgehead N-fused [5,6]-bicyclic heterocyclesRhodium (III)-catalyzed C–H functionalization of C-alkenyl azoles with sulfoxonium ylides for the synthesis of bridgehead N-fused [5, 6]-bicyclic heterocycles
year cv 201820182018
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/j.tet.2018.03.06210.1016/j.tet.2018.03.062
first author openalex HoangHoangHoang

Citations

OpenAlex
45
Scholar
44
DOI
10.1016/j.tet.2018.03.062
OpenAlex
W2794625820

Match decisions

  • doi merged · 1.00 · Run 18
2018 Rhodium(III)-Catalyzed Imidoyl C−H Activation for Annulations to Azolopyrimidines Organic Letters article journal CV OA GS

CV span

lines 309–311 · CV · published

30955. Halskov, K. M.; Witten, M. R.; Hoang, G. L.; Mercado, B. Q.; Ellman, J. A. “Rhodium(III)-310Catalyzed Imidoyl C−H Activation for Annulations to Azolopyrimidines” Org. Lett. 20, 2464–2467311(2018).

Institution fields

Peer reviewed
yes
First author
Halskov
Co-authors
Halskov, K. M.; Witten, M. R.; Hoang, G. L.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium(III)-Catalyzed Imidoyl C−H Activation for Annulations to AzolopyrimidinesRhodium(III)-Catalyzed Imidoyl C–H Activation for Annulations to AzolopyrimidinesRhodium (III)-catalyzed imidoyl C–H activation for annulations to azolopyrimidines
year cv 201820182018
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.8b0081610.1021/acs.orglett.8b00816
first author openalex HalskovHalskovHalskov

Citations

OpenAlex
105
Scholar
112
DOI
10.1021/acs.orglett.8b00816
OpenAlex
W2794632549

Match decisions

  • doi merged · 1.00 · Run 18
2018 Selective and Synergistic Cobalt(III)-Catalysed Three-Component C–H Bond Addition to Dienes and Aldehydes Nature Catalysis article journal CV OA GS

CV span

lines 289–291 · CV · published

28950. Boerth, J. A.; Maity, S.; Williams, S. K.; Mercado, B. Q.; Ellman, J. A. “Selective and Synergistic290Cobalt(III)-Catalysed Three-Component C–H Bond Addition to Dienes and Aldehydes” Nat. Catal.2911, 673–679 (2018).

Institution fields

Peer reviewed
yes
First author
Boerth
Co-authors
Boerth, J. A.; Maity, S.; Williams, S. K.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Selective and Synergistic Cobalt(III)-Catalysed Three-Component C–H Bond Addition to Dienes and AldehydesSelective and synergistic cobalt(iii)-catalysed three-component C–H bond addition to dienes and aldehydesSelective and synergistic cobalt(iii)-catalysed three-component C–H bond addition to dienes and aldehydes
year cv 201820182018
venue crossref Nat. Catal.Nature CatalysisNature catalysisNature Catalysis
kind cv articlearticleother
DOI crossref 10.1038/s41929-018-0123-410.1038/s41929-018-0123-4
first author openalex BoerthBoerthBoerth

Citations

OpenAlex
100
Scholar
95
DOI
10.1038/s41929-018-0123-4
OpenAlex
W2886440206

Match decisions

  • doi merged · 1.00 · Run 18
2018 Synthesis and Biological Evaluation of an Indazole-Based Selective Protein Arginine Deiminase 4 (PAD4) Inhibitor ACS Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 293–295 · CV · published

29351. Chandra Tjin, C.; Wissner, R.; Jamali, H.; Schepartz, A.; Ellman, J. A. “Synthesis and Biological294Evaluation of an Indazole-Based Selective Protein Arginine Deiminase 4 (PAD4) Inhibitor” ACS295Med. Chem. Lett. 9, 1013–1018 (2018).

Institution fields

Peer reviewed
yes
First author
Chandra Tjin
Co-authors
Chandra Tjin, C.; Wissner, R.; Jamali, H.; Schepartz, A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Biological Evaluation of an Indazole-Based Selective Protein Arginine Deiminase 4 (PAD4) InhibitorSynthesis and Biological Evaluation of an Indazole-Based Selective Protein Arginine Deiminase 4 (PAD4) Inhibitor
year cv 20182018
venue crossref ACS Med. Chem. Lett.ACS Medicinal Chemistry LettersACS Medicinal Chemistry Letters
kind cv articlearticle
DOI crossref 10.1021/acsmedchemlett.8b0028310.1021/acsmedchemlett.8b00283
first author openalex TjinTjin

Citations

OpenAlex
18
Scholar
none
DOI
10.1021/acsmedchemlett.8b00283
OpenAlex
W2891308088

Match decisions

  • doi merged · 1.00 · Run 18
2018 Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and Dioxazolones The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 297–299 · CV · published

29752. Hoang, G. L.; Halskov, K. M.; Ellman, J. A. “Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-298299Catalyzed Annulation of N-Azolo Imines and Dioxazolones” J. Org. Chem. 83, 9522–9529 (2018).

Institution fields

Peer reviewed
yes
First author
Hoang
Co-authors
Hoang, G. L.; Halskov, K. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and DioxazolonesSynthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and DioxazolonesSynthesis of Azolo [1, 3, 5] triazines via Rhodium (III)-Catalyzed Annulation of N‑Azolo Imines and Dioxazolones
year cv 201820182018
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.8b0124910.1021/acs.joc.8b01249
first author openalex HoangHoangHoang

Citations

OpenAlex
36
Scholar
42
DOI
10.1021/acs.joc.8b01249
OpenAlex
W2811401017

Match decisions

  • doi merged · 1.00 · Run 18
2018 Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5-a]pyrimidines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 285–287 · CV · published

28549. Hoang, G. L.; Streit, A. D.; Ellman, J. A. “Three-Component Coupling of Aldehydes,286Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation:287Synthesis of Pyrazolo[1,5-a]pyrimidines J. Org. Chem. 83, 15347–15360 (2018).

Institution fields

Peer reviewed
yes
First author
Hoang
Co-authors
Hoang, G. L.; Streit, A. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5-a]pyrimidinesThree-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo[1,5-a]pyrimidinesThree-Component Coupling of Aldehydes, Aminopyrazoles and Sulfoxonium Ylides via Rhodium (III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrazolo [1, 5-a] pyrimidines
year cv 201820182018
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.8b0260610.1021/acs.joc.8b02606
first author openalex HoangHoangHoang

Citations

OpenAlex
78
Scholar
85
DOI
10.1021/acs.joc.8b02606
OpenAlex
W2903852677

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/acs.joc.8b02606 for the pyrazolopyrimidines paper.
2017 A Convergent Synthesis of Functionalized Alkenyl Halides via Co(III)-Catalyzed Three-Component C-H Bond Addition Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 337–339 · CV · published

33761. Boerth, J. A.; Ellman, J. A. “A Convergent Synthesis of Functionalized Alkenyl Halides via338Co(III)-Catalyzed Three-Component C-H Bond Addition” Angew. Chem. Int. Ed. 56, 9976–9980339(2017).

Institution fields

Peer reviewed
yes
First author
Boerth
Co-authors
Boerth, J. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Convergent Synthesis of Functionalized Alkenyl Halides via Co(III)-Catalyzed Three-Component C-H Bond AdditionA Convergent Synthesis of Functionalized Alkenyl Halides through Cobalt(III)‐Catalyzed Three‐Component C−H Bond AdditionA Convergent Synthesis of Functionalized Alkenyl Halides through Cobalt(III)‐Catalyzed Three‐Component C−H Bond AdditionA Convergent Synthesis of Functionalized Alkenyl Halides through Cobalt (III)‐Catalyzed Three‐Component C− H Bond Addition
year cv 2017201720172017
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20170581710.1002/anie.20170581710.1002/ange.201705817
first author openalex BoerthBoerthBoerthBoerth

Also recorded as

  • W4243711099 (DOI 10.1002/ange.201705817) · platform twin · 2017 A Convergent Synthesis of Functionalized Alkenyl Halides through Cobalt(III)‐Catalyzed Three‐Component C−H Bond Addition

Citations

OpenAlex
88
Scholar
82
DOI
10.1002/anie.201705817
OpenAlex
W2724422844

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2017 Base-Controlled Completely Selective Linear or Branched Rhodium(I)-Catalyzed C−H ortho-Alkylation of Azines without Preactivation Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 353–355 · CV · published

35365. Tran, G.; Hesp, K. D.; Mascitti, V.; Ellman, J. A. “Base-Controlled Completely Selective Linear or354Branched Rhodium(I)-Catalyzed C−H ortho-Alkylation of Azines without Preactivation” Angew.355Chem. Int. Ed. 56, 5899–5903 (2017).

Institution fields

Peer reviewed
yes
First author
Tran
Co-authors
Tran, G.; Hesp, K. D.; Mascitti, V.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Base-Controlled Completely Selective Linear or Branched Rhodium(I)-Catalyzed C−H ortho-Alkylation of Azines without PreactivationBase‐Controlled Completely Selective Linear or Branched Rhodium(I)‐Catalyzed C−H ortho‐Alkylation of Azines without PreactivationBase‐Controlled Completely Selective Linear or Branched Rhodium(I)‐Catalyzed C−H ortho‐Alkylation of Azines without PreactivationBase‐Controlled Completely Selective Linear or Branched Rhodium(I)‐Catalyzed C−H ortho‐Alkylation of Azines without Preactivation
year cv 2017201720172017
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20170240910.1002/anie.20170240910.1002/ange.201702409
first author openalex TranTranTranTran

Also recorded as

  • W4243350004 (DOI 10.1002/ange.201702409) · same title · 2017 Base‐Controlled Completely Selective Linear or Branched Rhodium(I)‐Catalyzed C−H ortho‐Alkylation of Azines without Preactivation

Citations

OpenAlex
70
Scholar
66
DOI
10.1002/anie.201702409
OpenAlex
W2607168506

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2017 C2-Selective Branched Alkylation of Benzimidazoles by Rhodium(I)-Catalyzed C–H Activation The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 333–335 · CV · published

33360. Tran, G.; Confair, D.; Hesp, K. D.; Mascitti, V.; Ellman, J. A. “C2-Selective Branched Alkylation334of Benzimidazoles by Rhodium(I)-Catalyzed C–H Activation” J. Org. Chem. 82, 9243–9252335(2017).

Institution fields

Peer reviewed
yes
First author
Tran
Co-authors
Tran, G.; Confair, D.; Hesp, K. D.; Mascitti, V.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv C2-Selective Branched Alkylation of Benzimidazoles by Rhodium(I)-Catalyzed C–H ActivationC2-Selective Branched Alkylation of Benzimidazoles by Rhodium(I)-Catalyzed C–H ActivationC2-selective branched alkylation of benzimidazoles by rhodium (I)-catalyzed C–H activation
year cv 201720172017
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.7b0172310.1021/acs.joc.7b01723
first author openalex TranTranTran

Citations

OpenAlex
33
Scholar
35
DOI
10.1021/acs.joc.7b01723
OpenAlex
W2747607000

Match decisions

  • doi merged · 1.00 · Run 18
2017 Convergent Synthesis of α-Branched Amines by Transition-Metal-Catalyzed C−H Bond Additions to Imines Israel Journal of Chemistry article journal CV OA GS

CV span

lines 341–343 · CV · published

34162. Hummel, J. R.; Ellman, J. A. “Convergent Synthesis of α-Branched Amines by Transition-Metal-342Catalyzed C−H Bond Additions to Imines” Isr. J. Chem. 57, 916–931 (2017) [honoring Prof343Robert Bergman’s Wolf Prize].

Institution fields

Peer reviewed
yes
First author
Hummel
Co-authors
Hummel, J. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Convergent Synthesis of α-Branched Amines by Transition-Metal-Catalyzed C−H Bond Additions to IminesConvergent Synthesis of α‐Branched Amines by Transition‐Metal‐Catalyzed C−H Bond Additions to Imines
year cv 20172017
venue crossref Isr. J. Chem.Israel Journal of ChemistryIsrael Journal of Chemistry
kind cv articlearticle
DOI crossref 10.1002/ijch.20170002110.1002/ijch.201700021
first author openalex HummelHummel

Citations

OpenAlex
10
Scholar
none
DOI
10.1002/ijch.201700021
OpenAlex
W2727380915

Match decisions

  • doi merged · 1.00 · Run 18
2017 Glutathione-Responsive Selenosulfide Prodrugs as a Platform Strategy for Potent and Selective Mechanism-Based Inhibition of Protein Tyrosine Phosphatases ACS Central Science article journal CV OA GS

CV span

lines 323–326 · CV · published

32358. Tjin, C. C.; Otley, K. D.; Baguley, T. D.; Kurup, P.; Xu, J.; Nairn, A. C.; Lombroso, P. J.; Ellman,324J. A. “Glutathione-Responsive Selenosulfide Prodrugs as a Platform Strategy for Potent and325Selective Mechanism-Based Inhibition of Protein Tyrosine Phosphatases” ACS Cent. Sci. 3, 1322–3261328 (2017).

Institution fields

Peer reviewed
yes
First author
Tjin
Co-authors
Tjin, C. C.; Otley, K. D.; Baguley, T. D.; Kurup, P.; Xu, J.; Nairn, A. C.; Lombroso, P. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Glutathione-Responsive Selenosulfide Prodrugs as a Platform Strategy for Potent and Selective Mechanism-Based Inhibition of Protein Tyrosine PhosphatasesGlutathione-Responsive Selenosulfide Prodrugs as a Platform Strategy for Potent and Selective Mechanism-Based Inhibition of Protein Tyrosine Phosphatases
year cv 20172017
venue crossref ACS Cent. Sci.ACS Central ScienceACS Central Science
kind cv articlearticle
DOI crossref 10.1021/acscentsci.7b0048610.1021/acscentsci.7b00486
first author openalex TjinTjin

Citations

OpenAlex
22
Scholar
none
DOI
10.1021/acscentsci.7b00486
OpenAlex
W2772715504

Match decisions

  • doi merged · 1.00 · Run 18
2017 Rh(III)-Catalyzed Aryl and Alkenyl C–H Bond Addition to Diverse Nitroalkenes ACS Catalysis article journal CV OA GS

CV span

lines 360–361 · CV · published

36067. Potter, T. J.; Kamber, D. N.; Mercado, B. Q.; Ellman, J. A. “Rh(III)-Catalyzed Aryl and Alkenyl361C–H Bond Addition to Diverse Nitroalkenes” ACS Catal. 7, 150–153 (2017).

Institution fields

Peer reviewed
yes
First author
Potter
Co-authors
Potter, T. J.; Kamber, D. N.; Mercado, B. Q.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed Aryl and Alkenyl C–H Bond Addition to Diverse NitroalkenesRh(III)-Catalyzed Aryl and Alkenyl C–H Bond Addition to Diverse NitroalkenesRh (III)-catalyzed aryl and alkenyl C–H bond addition to diverse nitroalkenes
year cv 201720162017
venue crossref ACS Catal.ACS CatalysisACS catalysisACS Catalysis
kind cv articlearticleother
DOI crossref 10.1021/acscatal.6b0321710.1021/acscatal.6b03217
first author openalex PotterPotterPotter

Citations

OpenAlex
136
Scholar
136
DOI
10.1021/acscatal.6b03217
OpenAlex
W2558518728

Match decisions

  • doi merged · 1.00 · Run 18
2017 Synthesis of [5,6]-Bicyclic Heterocycles with a Ring-Junction Nitrogen via Rh(III)-Catalyzed C-H Functionalization of Alkenyl Azoles Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 345–347 · CV · published

34563. Halskov, K. M.; Roth, H.; Ellman, J. A. “Synthesis of [5,6]-Bicyclic Heterocycles with a Ring-346Junction Nitrogen via Rh(III)-Catalyzed C-H Functionalization of Alkenyl Azoles” Angew. Chem.347Int. Ed. 56, 9183–9187 (2017).

Institution fields

Peer reviewed
yes
First author
Halskov
Co-authors
Halskov, K. M.; Roth, H.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of [5,6]-Bicyclic Heterocycles with a Ring-Junction Nitrogen via Rh(III)-Catalyzed C-H Functionalization of Alkenyl AzolesSynthesis of [5,6]‐Bicyclic Heterocycles with a Ring‐Junction Nitrogen Atom: Rhodium(III)‐Catalyzed C−H Functionalization of Alkenyl AzolesSynthesis of [5,6]‐Bicyclic Heterocycles with a Ring‐Junction Nitrogen Atom: Rhodium(III)‐Catalyzed C−H Functionalization of Alkenyl AzolesSynthesis of [5, 6]‐Bicyclic Heterocycles with a Ring‐Junction Nitrogen Atom: Rhodium (III)‐Catalyzed C− H Functionalization of Alkenyl Azoles
year cv 2017201720172017
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20170396710.1002/anie.20170396710.1002/ange.201703967
first author openalex HalskovHalskovHalskovHalskov

Also recorded as

  • W4240897579 (DOI 10.1002/ange.201703967) · platform twin · 2017 Synthesis of [5,6]‐Bicyclic Heterocycles with a Ring‐Junction Nitrogen Atom: Rhodium(III)‐Catalyzed C−H Functionalization of Alkenyl Azoles

Citations

OpenAlex
67
Scholar
71
DOI
10.1002/anie.201703967
OpenAlex
W2623906574

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2017 Total Synthesis of (+)-Pancratistatin by the Rh(III)-Catalyzed Addition of a Densely Functionalized Benzamide to a Sugar-Derived Nitroalkene Organic Letters article journal CV OA GS

CV span

lines 349–351 · CV · published

34964. Potter, T. J.; Ellman, J. A. “Total Synthesis of (+)-Pancratistatin by the Rh(III)-Catalyzed Addition350of a Densely Functionalized Benzamide to a Sugar-Derived Nitroalkene” Org. Lett. 19, 2985–2988351(2017).

Institution fields

Peer reviewed
yes
First author
Potter
Co-authors
Potter, T. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Total Synthesis of (+)-Pancratistatin by the Rh(III)-Catalyzed Addition of a Densely Functionalized Benzamide to a Sugar-Derived NitroalkeneTotal Synthesis of (+)-Pancratistatin by the Rh(III)-Catalyzed Addition of a Densely Functionalized Benzamide to a Sugar-Derived NitroalkeneTotal synthesis of (+)-pancratistatin by the Rh (III)-catalyzed addition of a densely functionalized benzamide to a sugar-derived nitroalkene
year cv 201720172017
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.7b0122010.1021/acs.orglett.7b01220
first author openalex PotterPotterPotter

Citations

OpenAlex
31
Scholar
40
DOI
10.1021/acs.orglett.7b01220
OpenAlex
W2620087621

Match decisions

  • doi merged · 1.00 · Run 18
2017 Transition-Metal-Catalyzed C–H Bond Addition to Carbonyls, Imines, and Related Polarized π Bonds Chemical Reviews article journal CV OA GS

CV span

lines 357–358 · CV · published

35766. Hummel, J. R.; Boerth, J. A.; Ellman, J. A. “Transition-Metal-Catalyzed C–H Bond Addition to358Carbonyls, Imines, and Related Polarized π Bonds” Chem. Rev. 117, 9163–9227 (2017).

Institution fields

Peer reviewed
yes
First author
Hummel
Co-authors
Hummel, J. R.; Boerth, J. A.; Ellman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Transition-Metal-Catalyzed C–H Bond Addition to Carbonyls, Imines, and Related Polarized π BondsTransition-Metal-Catalyzed C–H Bond Addition to Carbonyls, Imines, and Related Polarized π BondsTransition-metal-catalyzed C–H bond addition to carbonyls, imines, and related polarized π bonds
year cv 201720162017
venue crossref Chem. Rev.Chemical ReviewsChemical ReviewsChemical Reviews
kind cv articlereviewother
DOI crossref 10.1021/acs.chemrev.6b0066110.1021/acs.chemrev.6b00661
first author openalex HummelHummelHummel

Citations

OpenAlex
744
Scholar
726
DOI
10.1021/acs.chemrev.6b00661
OpenAlex
W2564858020

Match decisions

  • doi merged · 1.00 · Run 18
2017 X-Ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase Inhibitors Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 328–331 · CV · published

32859. Witten, M. R.; Wissler, L.; Snow, M.; Geschwindner, S.; Read, J.; Brandon, M. J.; Nairn, A. C.;329Lombroso, P. J.; Käck, H.; Ellman, J. A. “X-Ray Characterization and Structure-Based330Optimization of Striatal-Enriched Protein Tyrosine Phosphatase Inhibitors” J. Med. Chem. 60,3319299–9319 (2017).

Institution fields

Peer reviewed
yes
First author
Witten
Co-authors
Witten, M. R.; Wissler, L.; Snow, M.; Geschwindner, S.; Read, J.; Brandon, M. J.; Nairn, A. C.; Lombroso, P. J.; Käck, H.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv X-Ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase InhibitorsX-ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase InhibitorsX‑ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase Inhibitors
year cv 201720172017
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.jmedchem.7b0129210.1021/acs.jmedchem.7b01292
first author openalex WittenWittenWitten

Citations

OpenAlex
30
Scholar
33
DOI
10.1021/acs.jmedchem.7b01292
OpenAlex
W2767592452

Match decisions

  • doi merged · 1.00 · Run 18
2016 4-(Diethylphosphino)-N,N-dimethylaniline Encyclopedia of Reagents for Organic Synthesis chapter journal CV OA GS

CV span

lines 394–395 · CV · published

39477. Mesganaw, T.; Elman, J. A. “4-(Diethylphosphino)-N,N-dimethylaniline” e-EROS Encyclopedia of395Reagents for Organic Synthesis (2016).

Institution fields

Peer reviewed
yes
First author
Mesganaw
Co-authors
Mesganaw, T.; Elman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv 4-(Diethylphosphino)-N,N-dimethylaniline4-(Diethylphosphino)-N,N-dimethylaniline
year cv 20162016
venue openalex e-EROS Encyclopedia of Reagents for Organic SynthesisEncyclopedia of Reagents for Organic Synthesis
kind cv chapterchapter
DOI openalex 10.1002/047084289x.rn01891
first author openalex MesganawMesganaw

Citations

OpenAlex
0
Scholar
none
DOI
10.1002/047084289x.rn01891
OpenAlex
W2788516784

Match decisions

  • fingerprint merged · 1.00 · Run 18
2016 Catalytic Enantioselective Addition of Pyrazol-5-ones to Trisubstituted Nitroalkenes with an N-Sulfinylurea Organocatalyst Advanced Synthesis & Catalysis article journal CV OA GS needs review

CV span

lines 387–388 · CV · published

38775. Phelan, J. P.; Ellman, J. A. “Catalytic Enantioselective Addition of Pyrazol-5-ones to Trisubstituted388Nitroalkenes with an N-Sulfinylurea Organocatalyst” Adv. Synth. Catal. 358, 1713–1718 (2016).

Institution fields

Peer reviewed
yes
First author
Phelan
Co-authors
Phelan, J. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Addition of Pyrazol-5-ones to Trisubstituted Nitroalkenes with an N-Sulfinylurea OrganocatalystCatalytic Enantioselective Addition of Pyrazol‐5‐ones to Trisubstituted Nitroalkenes with an N‐Sulfinylurea OrganocatalystCatalytic Enantioselective Addition of Pyrazol‐5‐ones to Trisubstituted Nitroalkenes with an N‐Sulfinylurea Organocatalyst
year cv 201620162016
venue crossref Adv. Synth. Catal.Advanced Synthesis & CatalysisAdvanced Synthesis & CatalysisAdvanced Synthesis & Catalysis
kind cv articlearticleother
DOI crossref 10.1002/adsc.20160011010.1002/adsc.201600110
first author openalex PhelanPhelanPhelan

Citations

OpenAlex
39
Scholar
36
DOI
10.1002/adsc.201600110
OpenAlex
W2346409431

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201406971 for catalytic enantioselective addition of thioacids.
  • doi merged · 1.00 · Run 18
2016 Cellular Activity of New Small Molecule Protein Arginine Deiminase 3 (PAD3) Inhibitors ACS Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 374–375 · CV · published

37471. Jamali, H.; Khan, H. A.; Tjin, C. C.; Ellman, J. A. “Cellular Activity of New Small Molecule375Protein Arginine Deiminase 3 (PAD3) Inhibitors” ACS Med. Chem. Lett. 7847–851 (2016).

Institution fields

Peer reviewed
yes
First author
Jamali
Co-authors
Jamali, H.; Khan, H. A.; Tjin, C. C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Cellular Activity of New Small Molecule Protein Arginine Deiminase 3 (PAD3) InhibitorsCellular Activity of New Small Molecule Protein Arginine Deiminase 3 (PAD3) Inhibitors
year cv 20162016
venue crossref ACS Med. Chem. Lett.ACS Medicinal Chemistry LettersACS Medicinal Chemistry Letters
kind cv articlearticle
DOI crossref 10.1021/acsmedchemlett.6b0021510.1021/acsmedchemlett.6b00215
first author openalex JamaliJamali

Citations

OpenAlex
21
Scholar
none
DOI
10.1021/acsmedchemlett.6b00215
OpenAlex
W2475660578

Match decisions

  • doi merged · 1.00 · Run 18
2016 Conjugate Addition–Enantioselective Protonation Reactions Beilstein Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 384–385 · CV · published

38474. Phelan, J. P.; Ellman, J. A. “Conjugate Addition–Enantioselective Protonation Reactions” Beilstein385J. Org. Chem. 12, 1203–1228 (2016).

Institution fields

Peer reviewed
yes
First author
Phelan
Co-authors
Phelan, J. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Conjugate Addition–Enantioselective Protonation ReactionsConjugate addition–enantioselective protonation reactionsConjugate addition–enantioselective protonation reactions
year cv 201620162016
venue crossref Beilstein J. Org. Chem.Beilstein Journal of Organic ChemistryBeilstein Journal of Organic ChemistryBeilstein Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.3762/bjoc.12.11610.3762/bjoc.12.116
first author openalex PhelanPhelanPhelan

Citations

OpenAlex
83
Scholar
73
DOI
10.3762/bjoc.12.116
OpenAlex
W2438431483

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.3762/bjoc.12.116 for conjugate addition-enantioselective protonation reactions.
  • doi merged · 1.00 · Run 18
2016 Convergent Synthesis of Diverse Nitrogen Heterocycles via Rh(III)-Catalyzed C–H Conjugate Addition/Cyclization Reactions Organic Letters article journal CV OA GS needs review

CV span

lines 377–379 · CV · published

37772. Weinstein, A. B.; Ellman, J. A. “Convergent Synthesis of Diverse Nitrogen Heterocycles via378Rh(III)-Catalyzed C–H Conjugate Addition/Cyclization Reactions” Org. Lett. 18, 3294-3297379(2016).

Institution fields

Peer reviewed
yes
First author
Weinstein
Co-authors
Weinstein, A. B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Convergent Synthesis of Diverse Nitrogen Heterocycles via Rh(III)-Catalyzed C–H Conjugate Addition/Cyclization ReactionsConvergent Synthesis of Diverse Nitrogen Heterocycles via Rh(III)-Catalyzed C–H Conjugate Addition/Cyclization ReactionsConvergent synthesis of diverse nitrogen heterocycles via Rh (III)-catalyzed C–H conjugate addition/cyclization reactions
year cv 201620162016
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.6b0161110.1021/acs.orglett.6b01611
first author openalex WeinsteinWeinsteinWeinstein

Citations

OpenAlex
40
Scholar
44
DOI
10.1021/acs.orglett.6b01611
OpenAlex
W2460638547

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.orglett.6b01611 for convergent synthesis of nitrogen heterocycles.
  • doi merged · 1.00 · Run 18
2016 Down-Regulation of BDNF in Cell and Animal Models Increases Striatal-Enriched Protein Tyrosine Phosphatase STEP61 Levels Journal of Neurochemistry article journal CV OA GS

CV span

lines 400–403 · CV · published

40079. Xu, J.; Kurup, P. K.; Azkona, G. M.; Baguley, T. D.; Saavedra, A. C.; Nairn, A. C.; Ellman, J. A.;401Perez-Navarro, E.; Lombroso, P. A. “Down-Regulation of BDNF in Cell and Animal Models402Increases Striatal-Enriched Protein Tyrosine Phosphatase STEP61 Levels” J. Neurochem. 136, 285–403294 (2016).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, J.; Kurup, P. K.; Azkona, G. M.; Baguley, T. D.; Saavedra, A. C.; Nairn, A. C.; Ellman, J. A.; Perez-Navarro, E.; Lombroso, P. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Down-Regulation of BDNF in Cell and Animal Models Increases Striatal-Enriched Protein Tyrosine Phosphatase STEP61 LevelsDown‐regulation of BDNF in cell and animal models increases striatal‐enriched protein tyrosine phosphatase 61 ( STEP 61) levelsDown‐regulation of BDNF in cell and animal models increases striatal‐enriched protein tyrosine phosphatase 61 (STEP61) levels
year cv 201620152016
venue crossref J. Neurochem.Journal of NeurochemistryJournal of neurochemistryJournal of Neurochemistry
kind cv articlearticleother
DOI crossref 10.1111/jnc.1329510.1111/jnc.13295
first author openalex XuXuXu

Citations

OpenAlex
18
Scholar
27
DOI
10.1111/jnc.13295
OpenAlex
W1905484325

Match decisions

  • doi merged · 1.00 · Run 18
2016 Highly Stereoselective Cobalt(III)-Catalyzed Three-Component C−H Bond Addition Cascade Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 381–383 · CV · published

38173. Boerth, J. A.; Hummel, J. R.; Ellman, J. A. “Highly Stereoselective Cobalt(III)-Catalyzed Three-382Component C−H Bond Addition Cascade” Angew. Chem. Int. Ed. 55, 12650-12654 (2016).383

Institution fields

Peer reviewed
yes
First author
Boerth
Co-authors
Boerth, J. A.; Hummel, J. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Stereoselective Cobalt(III)-Catalyzed Three-Component C−H Bond Addition CascadeHighly Stereoselective Cobalt(III)‐Catalyzed Three‐Component C−H Bond Addition CascadeHighly Stereoselective Cobalt(III)‐Catalyzed Three‐Component C−H Bond Addition CascadeHighly Stereoselective Cobalt (III)‐Catalyzed Three‐Component C− H Bond Addition Cascade
year cv 2016201620162016
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20160383110.1002/anie.20160383110.1002/ange.201603831
first author openalex BoerthBoerthBoerthBoerth

Also recorded as

Citations

OpenAlex
174
Scholar
160
DOI
10.1002/anie.201603831
OpenAlex
W2421354436

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2016 Inhibition of the Tyrosine Phosphatase STEP61 Restores BDNF Expression and Reverses Motor and Cognitive Deficits in Phencyclidine-Treated Mice Cellular and Molecular Life Sciences article journal CV OA GS

CV span

lines 405–407 · CV · published

40580. Xu, J.; Kurup, P.; Baguley, T. D.; Foscue, E.; Ellman, J. A.; Nairn, A. C.; Lombroso, P. J.406“Inhibition of the Tyrosine Phosphatase STEP61 Restores BDNF Expression and Reverses Motor407and Cognitive Deficits in Phencyclidine-Treated Mice” Cell. Mol. Life Sci. 73, 1503-1514 (2016).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, J.; Kurup, P.; Baguley, T. D.; Foscue, E.; Ellman, J. A.; Nairn, A. C.; Lombroso, P. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Inhibition of the Tyrosine Phosphatase STEP61 Restores BDNF Expression and Reverses Motor and Cognitive Deficits in Phencyclidine-Treated MiceInhibition of the tyrosine phosphatase STEP61 restores BDNF expression and reverses motor and cognitive deficits in phencyclidine-treated miceInhibition of the tyrosine phosphatase STEP61 restores BDNF expression and reverses motor and cognitive deficits in phencyclidine-treated mice
year cv 201620152016
venue crossref Cell. Mol. Life Sci.Cellular and Molecular Life SciencesCellular and Molecular Life SciencesCellular and Molecular Life Sciences
kind cv articlearticleother
DOI crossref 10.1007/s00018-015-2057-110.1007/s00018-015-2057-1
first author openalex XuXuXu

Citations

OpenAlex
31
Scholar
36
DOI
10.1007/s00018-015-2057-1
OpenAlex
W2189086584

Match decisions

  • doi merged · 1.00 · Run 18
2016 New Regio- and Stereoselective Cascades via Unstabilized Azomethine Ylide Cycloadditions for the Synthesis of Highly Substituted Tropane and Indolizidine Frameworks Journal of the American Chemical Society article journal CV OA GS

CV span

lines 363–366 · CV · published

36368. Chen, S.; Bacauanu, V.; Knecht, T.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A. “New Regio-364and Stereoselective Cascades via Unstabilized Azomethine Ylide Cycloadditions for the Synthesis365of Highly Substituted Tropane and Indolizidine Frameworks” J. Am. Chem. Soc. 138, 12664–36612670 (2016).

Institution fields

Peer reviewed
yes
First author
Chen
Co-authors
Chen, S.; Bacauanu, V.; Knecht, T.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv New Regio- and Stereoselective Cascades via Unstabilized Azomethine Ylide Cycloadditions for the Synthesis of Highly Substituted Tropane and Indolizidine FrameworksNew Regio- and Stereoselective Cascades via Unstabilized Azomethine Ylide Cycloadditions for the Synthesis of Highly Substituted Tropane and Indolizidine FrameworksNew regio-and stereoselective cascades via unstabilized azomethine ylide cycloadditions for the synthesis of highly substituted tropane and indolizidine frameworks
year cv 201620162016
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.6b0835510.1021/jacs.6b08355
first author openalex ChenChenChen

Citations

OpenAlex
28
Scholar
34
DOI
10.1021/jacs.6b08355
OpenAlex
W2521697590

Match decisions

  • doi merged · 1.00 · Run 18
2016 Preparation of Enantiomerically Pure Perfluorobutanesulfinamide and Its Application to the Asymmetric Synthesis of α-Amino Acids The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 390–392 · CV · published

39076. Wangweerawong, A.; Hummel, J. R.; Bergman, R. G.: Ellman, J. A. “Preparation of391Enantiomerically Pure Perfluorobutanesulfinamide and Its Application to the Asymmetric Synthesis392of α-Amino Acids” J. Org. Chem. 81, 1547-1557 (2016).

Institution fields

Peer reviewed
yes
First author
Wangweerawong
Co-authors
Wangweerawong, A.; Hummel, J. R.; Bergman, R. G.: Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Preparation of Enantiomerically Pure Perfluorobutanesulfinamide and Its Application to the Asymmetric Synthesis of α-Amino AcidsPreparation of Enantiomerically Pure Perfluorobutanesulfinamide and Its Application to the Asymmetric Synthesis of α-Amino AcidsPreparation of enantiomerically pure perfluorobutanesulfinamide and its application to the asymmetric synthesis of α-amino acids
year cv 201620162016
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.5b0270010.1021/acs.joc.5b02700
first author openalex WangweerawongWangweerawongWangweerawong

Citations

OpenAlex
36
Scholar
36
DOI
10.1021/acs.joc.5b02700
OpenAlex
W2268214136

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.joc.5b02700 for perfluorobutanesulfinamide application.
  • doi merged · 1.00 · Run 18
2016 Preparation of (S)-Nonafluorobutanesulfinamide Organic Syntheses article journal CV OA GS

CV span

lines 368–369 · CV · published

36869. Wangweerawong, A.; Kolmar. S.; Ellman, J. A. “Preparation of (S)-Nonafluorobutanesulfinamide”369Org. Synth. 93, 319-330 (2016).

Institution fields

Peer reviewed
yes
First author
Wangweerawong
Co-authors
Wangweerawong, A.; Kolmar. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of (S)-NonafluorobutanesulfinamidePreparation of (S)‐Nonafluorobutanesulfinamide
year cv 20162017
venue openalex Org. Synth.Organic Syntheses
kind cv articleother
DOI openalex 10.1002/0471264229.os093.23
first author openalex WangweerawongWangweerawong

Citations

OpenAlex
1
Scholar
none
DOI
10.1002/0471264229.os093.23
OpenAlex
W2537306215

Match decisions

  • fingerprint merged · 1.00 · Run 18
2016 Rh(III)-Catalyzed C–H Bond Addition/Amine-Mediated Cyclization of Bis-Michael Acceptors Organic Letters article journal CV OA GS needs review

CV span

lines 371–372 · CV · published

37170. Potter, T. J.; Ellman, J. A. “Rh(III)-Catalyzed C–H Bond Addition/Amine-Mediated Cyclization of372Bis-Michael Acceptors” Org. Lett. 18, 3838–3841 (2016).

Institution fields

Peer reviewed
yes
First author
Potter
Co-authors
Potter, T. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed C–H Bond Addition/Amine-Mediated Cyclization of Bis-Michael AcceptorsRh(III)-Catalyzed C–H Bond Addition/Amine-Mediated Cyclization of Bis-Michael AcceptorsRh (III)-Catalyzed C–H Bond Addition/Amine-Mediated Cyclization of Bis-Michael Acceptors
year cv 201620162016
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.6b0184610.1021/acs.orglett.6b01846
first author openalex PotterPotterPotter

Citations

OpenAlex
27
Scholar
28
DOI
10.1021/acs.orglett.6b01846
OpenAlex
W2505466489

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.orglett.6b01846 for rh(iii)-catalyzed C-H bond addition.
  • doi merged · 1.00 · Run 18
2016 Rh(III)-Catalyzed Diastereoselective C–H Bond Addition/Cyclization Cascade of Enone Tethered Aldehydes Chemical Science article journal CV OA GS

CV span

lines 397–398 · CV · published

39778. Boerth, J. A.; Ellman, J. A. “Rh(III)-Catalyzed Diastereoselective C–H Bond Addition/Cyclization398Cascade of Enone Tethered Aldehydes” Chem. Sci. 7, 1474-1479 (2016).

Institution fields

Peer reviewed
yes
First author
Boerth
Co-authors
Boerth, J. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed Diastereoselective C–H Bond Addition/Cyclization Cascade of Enone Tethered AldehydesRh( iii )-catalyzed diastereoselective C–H bond addition/cyclization cascade of enone tethered aldehydesRh(iii)-catalyzed diastereoselective C–H bond addition/cyclization cascade of enone tethered aldehydes
year cv 201620152016
venue crossref Chem. Sci.Chemical ScienceChemical ScienceChemical Science
kind cv articlearticleother
DOI crossref 10.1039/c5sc04138d10.1039/c5sc04138d
first author openalex BoerthBoerthBoerth

Citations

OpenAlex
102
Scholar
100
DOI
10.1039/c5sc04138d
OpenAlex
W2187855276

Match decisions

  • doi merged · 1.00 · Run 18
2016 STEP Modulates Nociception: Evidences from Genetic Deletion and Pharmacological Inhibition Pain article journal CV OA GS

CV span

lines 409–411 · CV · published

40981. Azkona, G.; Saavedra, A.; Aira, Z.; Aluja, D.; Xifró, X.; Baguley, T.; Alberch, J.; Ellman, J. A.;410Lombroso, P.J.; Azkue, J.J.; Pérez-Navarro, E. “STEP Modulates Nociception: Evidences from411Genetic Deletion and Pharmacological Inhibition” Pain 157, 377-86 (2016).

Institution fields

Peer reviewed
yes
First author
Azkona
Co-authors
Azkona, G.; Saavedra, A.; Aira, Z.; Aluja, D.; Xifró, X.; Baguley, T.; Alberch, J.; Ellman, J. A.; Lombroso, P.J.; Azkue, J.J.; Pérez-Navarro, E.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv STEP Modulates Nociception: Evidences from Genetic Deletion and Pharmacological InhibitionStriatal-enriched protein tyrosine phosphatase modulates nociception
year cv 20162015
venue openalex PainPain
kind cv articlearticle
DOI crossref 10.1097/j.pain.000000000000032910.1097/j.pain.0000000000000329
first author openalex AzkonaAzkona

Citations

OpenAlex
19
Scholar
none
DOI
10.1097/j.pain.0000000000000329
OpenAlex
W2408813734

Match decisions

  • doi merged · 1.00 · Run 18
2015 An Efficient Method for the Preparation of Styrene Derivatives via Rh(III)-Catalyzed Direct C–H Vinylation Organic Letters article journal CV OA GS needs review

CV span

lines 442–443 · CV · published

44289. Otley, K. D.; Ellman, J. A. “An Efficient Method for the Preparation of Styrene Derivatives via443Rh(III)-Catalyzed Direct C–H Vinylation” Org. Lett. 17, 1332–1335 (2015).

Institution fields

Peer reviewed
yes
First author
Otley
Co-authors
Otley, K. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv An Efficient Method for the Preparation of Styrene Derivatives via Rh(III)-Catalyzed Direct C–H VinylationAn Efficient Method for the Preparation of Styrene Derivatives via Rh(III)-Catalyzed Direct C–H VinylationAn Efficient Method for the Preparation of Styrene Derivatives via Rh (III)-Catalyzed Direct C—H Vinylation
year cv 201520152015
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.5b0034010.1021/acs.orglett.5b00340
first author openalex OtleyOtleyOtley

Citations

OpenAlex
70
Scholar
72
DOI
10.1021/acs.orglett.5b00340
OpenAlex
W2320453407

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.orglett.5b00340 for styrene derivatives via direct C-H vinylation.
  • doi merged · 1.00 · Run 18
2015 Cobalt(III)-Catalyzed C–H Bond Amidation with Isocyanates Organic Letters article journal CV OA GS needs review

CV span

lines 430–431 · CV · published

43086. Hummel, J. R.; Ellman, J. A. “Cobalt(III)-Catalyzed C–H Bond Amidation with Isocyanates” Org.431Lett. 17, 2400–2403 (2015).

Institution fields

Peer reviewed
yes
First author
Hummel
Co-authors
Hummel, J. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Cobalt(III)-Catalyzed C–H Bond Amidation with IsocyanatesCobalt(III)-Catalyzed C–H Bond Amidation with IsocyanatesCobalt (III)-catalyzed C–H bond amidation with isocyanates
year cv 201520152015
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.5b0091010.1021/acs.orglett.5b00910
first author openalex HummelHummelHummel

Citations

OpenAlex
164
Scholar
162
DOI
10.1021/acs.orglett.5b00910
OpenAlex
W2460846234

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.orglett.5b00910 for cobalt(iii)-catalyzed C-H amidation with isocyanates.
  • doi merged · 1.00 · Run 18
2015 Cobalt(III)-Catalyzed Synthesis of Indazoles and Furans by C–H Bond Functionalization/Addition/Cyclization Cascades Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 452–453 · CV · published

45292. Hummel, J. R.; Ellman, J. A. “Cobalt(III)-Catalyzed Synthesis of Indazoles and Furans by C–H453Bond Functionalization/Addition/Cyclization Cascades” J. Am. Chem. Soc. 137, 490–498 (2015).

Institution fields

Peer reviewed
yes
First author
Hummel
Co-authors
Hummel, J. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Cobalt(III)-Catalyzed Synthesis of Indazoles and Furans by C–H Bond Functionalization/Addition/Cyclization CascadesCobalt(III)-Catalyzed Synthesis of Indazoles and Furans by C–H Bond Functionalization/Addition/Cyclization CascadesCobalt (III)-catalyzed synthesis of indazoles and furans by C–H bond functionalization/addition/cyclization cascades
year cv 201520142015
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja511645210.1021/ja5116452
first author openalex HummelHummelHummel

Citations

OpenAlex
437
Scholar
449
DOI
10.1021/ja5116452
OpenAlex
W1976613964

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja5116452 for the cobalt(III)-catalyzed synthesis of indazoles.
  • doi merged · 1.00 · Run 18
2015 Design of a Highly Selective Quenched Activity-Based Probe and Its Application in Dual Color Imaging Studies of Cathepsin S Activity Localization Journal of the American Chemical Society article journal CV OA GS

CV span

lines 433–436 · CV · published

43387. Oresic Bender, K.; Ofori, L.; van der Linden, W. A.; Mock, E. D.; Datta, G.; Chowdhury, S.; Li,434H.; Segal, E.; Lopez, M. S.; Ellman, J. A.; Figdor, C. G.; Bogyo, M.; Verdoes, M. “Design of a435Highly Selective Quenched Activity-Based Probe and Its Application in Dual Color Imaging436Studies of Cathepsin S Activity Localization” J. Am. Chem. Soc. 137, 4771–4777 (2015).

Institution fields

Peer reviewed
yes
First author
Oresic Bender
Co-authors
Oresic Bender, K.; Ofori, L.; van der Linden, W. A.; Mock, E. D.; Datta, G.; Chowdhury, S.; Li, H.; Segal, E.; Lopez, M. S.; Ellman, J. A.; Figdor, C. G.; Bogyo, M.; Verdoes, M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design of a Highly Selective Quenched Activity-Based Probe and Its Application in Dual Color Imaging Studies of Cathepsin S Activity LocalizationDesign of a Highly Selective Quenched Activity-Based Probe and Its Application in Dual Color Imaging Studies of Cathepsin S Activity LocalizationDesign of a highly selective quenched activity-based probe and its application in dual color imaging studies of cathepsin S activity localization
year cv 201520152015
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.5b0031510.1021/jacs.5b00315
first author openalex BenderBenderBender

Citations

OpenAlex
75
Scholar
86
DOI
10.1021/jacs.5b00315
OpenAlex
W1990590874

Match decisions

  • doi merged · 1.00 · Run 18
2015 Facile Rh(III)-Catalyzed Synthesis of Fluorinated Pyridines Organic Letters article journal CV OA GS needs review

CV span

lines 427–428 · CV · published

42785. Chen, S.; Bergman, R. G.; Ellman, J. A. “Facile Rh(III)-Catalyzed Synthesis of Fluorinated428Pyridines” 17, Org. Lett. 2567–2569 (2015).

Institution fields

Peer reviewed
yes
First author
Chen
Co-authors
Chen, S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Facile Rh(III)-Catalyzed Synthesis of Fluorinated PyridinesFacile Rh(III)-Catalyzed Synthesis of Fluorinated PyridinesFacile Rh (III)-catalyzed synthesis of fluorinated pyridines
year cv 201520152015
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/acs.orglett.5b0097910.1021/acs.orglett.5b00979
first author openalex ChenChenChen

Citations

OpenAlex
44
Scholar
41
DOI
10.1021/acs.orglett.5b00979
OpenAlex
W2400670772

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.orglett.5b00979 for fluorinated pyridines synthesis.
  • doi merged · 1.00 · Run 18
2015 Identification of Multiple Structurally-Distinct, Nonpeptidic Small Molecule Inhibitors of Protein Arginine Deiminase 3 Using a Substrate-Based Fragment Method Journal of the American Chemical Society article journal CV OA GS

CV span

lines 438–441 · CV · published

43888. Jamali, H.; Khan, H. A.; Stringer, J. A.; Chowdhury, S.; Ellman, J. A. “Identification of Multiple439Structurally-Distinct, Nonpeptidic Small Molecule Inhibitors of Protein Arginine Deiminase 3440Using a Substrate-Based Fragment Method” J. Am. Chem. Soc. 137, 3616–3621 (2015).441

Institution fields

Peer reviewed
yes
First author
Jamali
Co-authors
Jamali, H.; Khan, H. A.; Stringer, J. A.; Chowdhury, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of Multiple Structurally-Distinct, Nonpeptidic Small Molecule Inhibitors of Protein Arginine Deiminase 3 Using a Substrate-Based Fragment MethodIdentification of Multiple Structurally Distinct, Nonpeptidic Small Molecule Inhibitors of Protein Arginine Deiminase 3 Using a Substrate-Based Fragment MethodIdentification of multiple structurally distinct, nonpeptidic small molecule inhibitors of protein arginine deiminase 3 using a substrate-based fragment method
year cv 201520152015
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/jacs.5b0009510.1021/jacs.5b00095
first author openalex JamaliJamaliJamali

Citations

OpenAlex
31
Scholar
39
DOI
10.1021/jacs.5b00095
OpenAlex
W2323234720

Match decisions

  • doi merged · 1.00 · Run 18
2015 Regio- and Diastereoselective Synthesis of Highly Substituted, Oxygenated Piperidines from Tetrahydropyridines The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 423–425 · CV · published

42384. Chen, S.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A. “Regio- and Diastereoselective Synthesis424of Highly Substituted, Oxygenated Piperidines from Tetrahydropyridines” J. Org. Chem. 80, 6660–4256668 (2015).

Institution fields

Peer reviewed
yes
First author
Chen
Co-authors
Chen, S.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Regio- and Diastereoselective Synthesis of Highly Substituted, Oxygenated Piperidines from TetrahydropyridinesRegio- and Diastereoselective Synthesis of Highly Substituted, Oxygenated Piperidines from TetrahydropyridinesRegio-and diastereoselective synthesis of highly substituted, oxygenated piperidines from tetrahydropyridines
year cv 201520152015
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/acs.joc.5b0081610.1021/acs.joc.5b00816
first author openalex ChenChenChen

Citations

OpenAlex
26
Scholar
27
DOI
10.1021/acs.joc.5b00816
OpenAlex
W2469150884

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/acs.joc.5b00816 for synthesis of oxygenated piperidines.
  • doi merged · 1.00 · Run 18
2015 Rh(I)-Catalyzed Cycloisomerization of 1,6-Enynes Synlett article journal CV OA GS needs review

CV span

lines 445–446 · CV · published

44590. Matsushima, Y.; Phillips, E. M.; Bergman, R. G.; Ellman, J. A. “Rh(I)-Catalyzed446Cycloisomerization of 1,6-Enynes” Synlett 26, 1533–1536 (2015) [Issue honoring Peter Vollhardt].

Institution fields

Peer reviewed
yes
First author
Matsushima
Co-authors
Matsushima, Y.; Phillips, E. M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Rh(I)-Catalyzed Cycloisomerization of 1,6-EnynesRhodium(I)-Catalyzed Cycloisomerization of 1,6-Enynes
year cv 20152015
venue crossref SynlettSynlett
kind cv articlearticle
DOI crossref 10.1055/s-0034-138035910.1055/s-0034-1380359
first author openalex MatsushimaEllman

Citations

OpenAlex
5
Scholar
none
DOI
10.1055/s-0034-1380359
OpenAlex
W2175023044

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1055/s-0034-1380359 for rhodium(i)-catalyzed cycloisomerization.
  • doi merged · 1.00 · Run 18
2015 Synthesis of Benzopentathiepin Analogs and Their Evaluation as Inhibitors of the Phosphatase STEP Bioorganic & Medicinal Chemistry Letters article journal CV OA GS needs review

CV span

lines 448–450 · CV · published

44891. Baguley, T. D.; Nairn, A. C.; Lombroso, P. J.; Ellman, J. A. “Synthesis of Benzopentathiepin449Analogs and Their Evaluation as Inhibitors of the Phosphatase STEP” Bioorg. Med. Chem. Lett. 25,4501050-1052 (2015).

Institution fields

Peer reviewed
yes
First author
Baguley
Co-authors
Baguley, T. D.; Nairn, A. C.; Lombroso, P. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Benzopentathiepin Analogs and Their Evaluation as Inhibitors of the Phosphatase STEPSynthesis of benzopentathiepin analogs and their evaluation as inhibitors of the phosphatase STEP
year cv 20152015
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & Medicinal Chemistry Letters
kind cv articlearticle
DOI crossref 10.1016/j.bmcl.2015.01.02010.1016/j.bmcl.2015.01.020
first author openalex BaguleyBaguley

Citations

OpenAlex
12
Scholar
none
DOI
10.1016/j.bmcl.2015.01.020
OpenAlex
W2090687485

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/j.bmcl.2015.01.020 for benzopentathiepin analogs.
  • doi merged · 1.00 · Run 18
2015 Synthesis of ent-Ketorfanol via a C–H Alkenylation/ Torquoselective 6π-Electrocyclization Cascade Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 413–415 · CV · published

41382. Phillips, E. M.; Mesganaw, T.; Patel, A. Duttwyler, S.; Mercado, B. Q.; Houk, K. N.; Ellman, J. A.414“Synthesis of ent-Ketorfanol via a C–H Alkenylation/ Torquoselective 6π-Electrocyclization415Cascade” Angew. Chem. Int. Ed. 54, 12044–12048 (2015).

Institution fields

Peer reviewed
yes
First author
Phillips
Co-authors
Phillips, E. M.; Mesganaw, T.; Patel, A. Duttwyler, S.; Mercado, B. Q.; Houk, K. N.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of ent-Ketorfanol via a C–H Alkenylation/ Torquoselective 6π-Electrocyclization CascadeSynthesis of ent‐Ketorfanol via a C–H Alkenylation/Torquoselective 6π Electrocyclization CascadeSynthesis of ent‐Ketorfanol via a C–H Alkenylation/Torquoselective 6π Electrocyclization CascadeSynthesis of ent‐Ketorfanol via a C–H Alkenylation/Torquoselective 6π Electrocyclization Cascade
year cv 2015201520152015
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20150560410.1002/anie.20150560410.1002/ange.201505604
first author openalex PhillipsPhillipsPhillipsPhillips

Also recorded as

  • W4253995813 (DOI 10.1002/ange.201505604) · same title · 2015 Synthesis of ent‐Ketorfanol via a C–H Alkenylation/Torquoselective 6π Electrocyclization Cascade

Citations

OpenAlex
36
Scholar
43
DOI
10.1002/anie.201505604
OpenAlex
W2117864656

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2015 Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors with Improved Pharmacokinetic Properties as Therapeutic Leads for Chagas’ Disease Bioorganic & Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 417–421 · CV · published

41783. Neitz, R. J.; Bryant, C.; Chen, S.; Gut, J.; Caselli, E. H.; Ponce, S.; Chowdhury, S.; Xu, H.; Arkin,418M. R.; Ellman, J. A.; Renslo, A. R. “Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors with419Improved Pharmacokinetic Properties as Therapeutic Leads for Chagas’ Disease” Bioorg. Med.420Chem. Lett. 25, 4834–4837 (2015) [Symposium-in-Print entitled ‘Recent Advances in Medicinal421Chemistry and Chemical Biology’ in celebration of the 25th anniversary of BMCL].

Institution fields

Peer reviewed
yes
First author
Neitz
Co-authors
Neitz, R. J.; Bryant, C.; Chen, S.; Gut, J.; Caselli, E. H.; Ponce, S.; Chowdhury, S.; Xu, H.; Arkin, M. R.; Ellman, J. A.; Renslo, A. R.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors with Improved Pharmacokinetic Properties as Therapeutic Leads for Chagas’ DiseaseTetrafluorophenoxymethyl ketone cruzain inhibitors with improved pharmacokinetic properties as therapeutic leads for Chagas’ diseaseTetrafluorophenoxymethyl ketone cruzain inhibitors with improved pharmacokinetic properties as therapeutic leads for Chagas’ disease
year cv 201520152015
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic & Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/j.bmcl.2015.06.06610.1016/j.bmcl.2015.06.066
first author openalex NeitzNeitzNeitz

Citations

OpenAlex
23
Scholar
30
DOI
10.1016/j.bmcl.2015.06.066
OpenAlex
W835383653

Match decisions

  • doi merged · 1.00 · Run 18
2014 A Lewis Acid-Catalyzed Annulation to 2,1-Benzisoxazoles The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 455–456 · CV · published

45593. Otley, K. D.; Ellman, J. A. “A Lewis Acid-Catalyzed Annulation to 2,1-Benzisoxazoles” J. Org.456Chem. 79, 8296–8303 (2014).

Institution fields

Peer reviewed
yes
First author
Otley
Co-authors
Otley, K. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Lewis Acid-Catalyzed Annulation to 2,1-BenzisoxazolesA Lewis Acid Catalyzed Annulation to 2,1-BenzisoxazolesA Lewis Acid Catalyzed Annulation to 2, 1-Benzisoxazoles
year cv 201420142014
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo501543210.1021/jo5015432
first author openalex OtleyOtleyOtley

Citations

OpenAlex
20
Scholar
27
DOI
10.1021/jo5015432
OpenAlex
W2060076424

Match decisions

  • doi merged · 1.00 · Run 18
2014 Asymmetric Synthesis of Protected α-Amino Boronic Acid Derivatives with an Air- and Moisture-Stable Cu(II) Catalyst The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 482–484 · CV · published

482100. Buesking, A. W.; Bacauanu, V.; Cai, I.; Ellman, J. A. “Asymmetric Synthesis of Protected α-483Amino Boronic Acid Derivatives with an Air- and Moisture-Stable Cu(II) Catalyst” J. Org. Chem.48479, 3671–3677 (2014).

Institution fields

Peer reviewed
yes
First author
Buesking
Co-authors
Buesking, A. W.; Bacauanu, V.; Cai, I.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Protected α-Amino Boronic Acid Derivatives with an Air- and Moisture-Stable Cu(II) CatalystAsymmetric Synthesis of Protected α-Amino Boronic Acid Derivatives with an Air- and Moisture-Stable Cu(II) CatalystAsymmetric synthesis of protected α-amino boronic acid derivatives with an air-and moisture-stable Cu (II) catalyst
year cv 201420142014
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo500300t10.1021/jo500300t
first author openalex BueskingBueskingBuesking

Citations

OpenAlex
85
Scholar
92
DOI
10.1021/jo500300t
OpenAlex
W2019905159

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo500300t for asymmetric synthesis of amino boronic acid derivatives.
  • doi merged · 1.00 · Run 18
2014 Asymmetric Synthesis of α-Branched Amines via Rh(III)-Catalyzed C–H Bond Functionalization Journal of the American Chemical Society article journal CV OA GS

CV span

lines 474–476 · CV · published

47498. Wangweerawong, A.; Bergman, R. G.; Ellman, J. A. “Asymmetric Synthesis of α-Branched475Amines via Rh(III)-Catalyzed C–H Bond Functionalization” J. Am. Chem. Soc. 136, 8520-8523476(2014) [Research highlight Nature Chem. 6, 656 (2014)].

Institution fields

Peer reviewed
yes
First author
Wangweerawong
Co-authors
Wangweerawong, A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of α-Branched Amines via Rh(III)-Catalyzed C–H Bond FunctionalizationAsymmetric Synthesis of α-Branched Amines via Rh(III)-Catalyzed C–H Bond FunctionalizationAsymmetric synthesis of α-branched amines via Rh (III)-catalyzed C–H bond functionalization
year cv 201420142014
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja503345210.1021/ja5033452
first author openalex WangweerawongWangweerawongWangweerawong

Citations

OpenAlex
93
Scholar
99
DOI
10.1021/ja5033452
OpenAlex
W2317863688

Match decisions

  • doi merged · 1.00 · Run 18
2014 Catalytic Enantioselective Addition of Thioacids to Trisubstituted Nitroalkenes Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 465–466 · CV · published

46596. Phelan, J. P.; Patel, E. J.; Ellman, J. A. “Catalytic Enantioselective Addition of Thioacids to466Trisubstituted Nitroalkenes” Angew. Chem. Int. Ed. 53, 11329–11332 (2014).

Institution fields

Peer reviewed
yes
First author
Phelan
Co-authors
Phelan, J. P.; Patel, E. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Addition of Thioacids to Trisubstituted NitroalkenesCatalytic Enantioselective Addition of Thioacids to Trisubstituted NitroalkenesCatalytic Enantioselective Addition of Thioacids to Trisubstituted NitroalkenesCatalytic enantioselective addition of thioacids to trisubstituted nitroalkenes
year cv 2014201420142014
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20140697110.1002/anie.20140697110.1002/ange.201406971
first author openalex PhelanPhelanPhelanPhelan

Also recorded as

Citations

OpenAlex
56
Scholar
58
DOI
10.1002/anie.201406971
OpenAlex
W1979264465

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201406971 for catalytic enantioselective addition of thioacids.
  • doi merged · 1.00 · Run 18
2014 Convergent, Asymmetric Synthesis of Vicinal Amino Alcohols via Rh-Catalyzed Addition of α-Amido Trifluoroborates to Carbonyls Chem. Sci. article journal CV OA GS needs review

CV span

lines 486–488 · CV · published

486101. Buesking, A. W.; Ellman, J. A. “Convergent, Asymmetric Synthesis of Vicinal Amino Alcohols via487Rh-Catalyzed Addition of α-Amido Trifluoroborates to Carbonyls” Chem. Sci. 5, 1983-1987488(2014).

Institution fields

Peer reviewed
yes
First author
Buesking
Co-authors
Buesking, A. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Convergent, Asymmetric Synthesis of Vicinal Amino Alcohols via Rh-Catalyzed Addition of α-Amido Trifluoroborates to CarbonylsConvergent, asymmetric synthesis of vicinal amino alcohols via Rh-catalyzed addition of α-amido trifluoroborates to carbonylsConvergent, asymmetric synthesis of vicinal amino alcohols via Rh-catalyzed addition of α-amido trifluoroborates to carbonyls
year cv 201420142014
venue crossref Chem. Sci.Chemical ScienceChemical Science
kind cv articlearticleother
DOI crossref 10.1039/c4sc00084f10.1039/c4sc00084f
first author openalex BueskingBueskingBuesking

Citations

OpenAlex
39
Scholar
41
DOI
10.1039/c4sc00084f
OpenAlex
W1965353616

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1039/c4sc00084f for asymmetric synthesis of vicinal amino alcohols.
  • doi merged · 1.00 · Run 18
2014 Convergent Synthesis of Diverse Tetrahydropyridines via Rh(I)-Catalyzed C–H Functionalization Sequences Organic Process Research & Development article journal CV OA GS needs review

CV span

lines 458–460 · CV · published

45894. Mesganaw, T.; Ellman, J. A. “Convergent Synthesis of Diverse Tetrahydropyridines via Rh(I)-459Catalyzed C–H Functionalization Sequences” Org. Process. Res. Dev. 18, 1097–1104 (2014).460

Institution fields

Peer reviewed
yes
First author
Mesganaw
Co-authors
Mesganaw, T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Convergent Synthesis of Diverse Tetrahydropyridines via Rh(I)-Catalyzed C–H Functionalization SequencesConvergent Synthesis of Diverse Tetrahydropyridines via Rh(I)-Catalyzed C–H Functionalization SequencesConvergent Synthesis of Diverse Tetrahydropyridines via Rh (I)-Catalyzed C–H Functionalization Sequences
year cv 201420142014
venue crossref Org. Process. Res. Dev.Organic Process Research & DevelopmentOrganic Process Research & DevelopmentOrganic Process Research & Development
kind cv articlearticleother
DOI crossref 10.1021/op500224x10.1021/op500224x
first author openalex MesganawMesganawMesganaw

Citations

OpenAlex
86
Scholar
88
DOI
10.1021/op500224x
OpenAlex
W2321177311

Match decisions

  • passthrough_guard not merged · 0.80 · low_confidence · Run 18 Multiple very closely related process chemistry papers on tetrahydropyridines from the same authors sharing similar DOIs in OPRD.
  • doi merged · 1.00 · Run 18
2014 Inhibitor of the Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer’s Disease PLoS Biology article journal CV OA GS

CV span

lines 468–472 · CV · published

46897. Xu, J.; Chatterjee, M.; Baguley, T. D.; Brouillette, J.; Kurup, P.; Ghosh, D.; Kanyo, J.; Zhang, Y.;469Seyb, K.; Ononenyi, C.; Foscue, E.; Anderson, G. M.; Gresack, J.; Cuny, G. D.; Glicksman, M. A.;470Greengard, P.; Lam, T. T.; Tautz, L.; Nairn, A. C.; Ellman, J. A.; Lombroso, P. A. “Inhibitor of the471Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer’s472Disease” PLoS Biol. 12, e1001923 (2014).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, J.; Chatterjee, M.; Baguley, T. D.; Brouillette, J.; Kurup, P.; Ghosh, D.; Kanyo, J.; Zhang, Y.; Seyb, K.; Ononenyi, C.; Foscue, E.; Anderson, G. M.; Gresack, J.; Cuny, G. D.; Glicksman, M. A.; Greengard, P.; Lam, T. T.; Tautz, L.; Nairn, A. C.; Ellman, J. A.; Lombroso, P. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Inhibitor of the Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer’s DiseaseInhibitor of the Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer's DiseaseInhibitor of the tyrosine phosphatase STEP reverses cognitive deficits in a mouse model of Alzheimer's disease
year cv 201420142014
venue crossref PLoS Biol.PLoS BiologyPLoS biologyPLoS Biology
kind cv articlearticleother
DOI crossref 10.1371/journal.pbio.100192310.1371/journal.pbio.1001923
first author openalex XuXuXu

Citations

OpenAlex
144
Scholar
161
DOI
10.1371/journal.pbio.1001923
OpenAlex
W1998328961

Match decisions

  • doi merged · 1.00 · Run 18
2014 Preparative Synthesis of Highly Substituted Tetrahydropyridines via a Rh(I)-Catalyzed C–H Functionalization Sequence Organic Process Research & Development article journal CV OA GS needs review

CV span

lines 461–463 · CV · published

46195. Mesganaw, T.; Ellman, J. A. “Preparative Synthesis of Highly Substituted Tetrahydropyridines via462a Rh(I)-Catalyzed C–H Functionalization Sequence” Org. Process. Res. Dev. 18, 1105–1109463(2014).

Institution fields

Peer reviewed
yes
First author
Mesganaw
Co-authors
Mesganaw, T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Preparative Synthesis of Highly Substituted Tetrahydropyridines via a Rh(I)-Catalyzed C–H Functionalization SequencePreparative Synthesis of Highly Substituted Tetrahydropyridines via a Rh(I)-Catalyzed C–H Functionalization Sequence
year cv 20142014
venue crossref Org. Process. Res. Dev.Organic Process Research & DevelopmentOrganic Process Research & Development
kind cv articlearticle
DOI crossref 10.1021/op500225c10.1021/op500225c
first author openalex MesganawMesganaw

Citations

OpenAlex
13
Scholar
none
DOI
10.1021/op500225c
OpenAlex
W2319402093

Match decisions

  • passthrough_guard not merged · 0.80 · low_confidence · Run 18 Multiple very closely related process chemistry papers on tetrahydropyridines from the same authors sharing similar DOIs in OPRD.
  • doi merged · 1.00 · Run 18
2014 Real-Time, Single-Step Bioassay using Nanoplasmonic Resonator with Ultra-High Sensitivity U.S. Patent No. 8,685,743 article CV OA GS

CV span

lines 1405–1407 · CV · published

14054. Zhang, X.; Chen, F.; Ellman, J. A.; Sun, C.; Su, K.-H.; Wei, Q.-H. “Real-Time, Single-Step1406Bioassay using Nanoplasmonic Resonator with Ultra-High Sensitivity” U.S. (2014), Patent No.14078,685,743.

Institution fields

Peer reviewed
none
First author
Zhang
Co-authors
Zhang, X.; Chen, F.; Ellman, J. A.; Sun, C.; Su, K.-H.; Wei, Q.-H.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Real-Time, Single-Step Bioassay using Nanoplasmonic Resonator with Ultra-High SensitivityReal-Time, Single-Step Bioassay Using Nanoplasmonic Resonator With Ultra-High Sensitivity
year cv 20142023
venue cv U.S. Patent No. 8,685,743NASA STI Repository (National Aeronautics and Space Administration)
kind openalex otherarticle
first author cv ZhangChen

Also recorded as

  • W4307652359 · same title · 2023 Real-Time, Single-Step Bioassay Using Nanoplasmonic Resonator With Ultra-High Sensitivity

Citations

OpenAlex
0
Scholar
none

Match decisions

  • alternate merged · 1.00 · Run 18
2014 Regio- and Stereoselective 1,2-Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary Centers Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 478–480 · CV · published

47899. Duttwyler, S.; Chen, S.; Lu, C.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A. “Regio- and479Stereoselective 1,2-Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines480with Quaternary Centers” Angew. Chem. Int. Ed. 53, 3877–3880 (2014).

Institution fields

Peer reviewed
yes
First author
Duttwyler
Co-authors
Duttwyler, S.; Chen, S.; Lu, C.; Mercado, B. Q.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Regio- and Stereoselective 1,2-Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary CentersRegio‐ and Stereoselective 1,2‐Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary CentersRegio‐ and Stereoselective 1,2‐Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary CentersRegio‐and Stereoselective 1, 2‐Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary Centers
year cv 2014201420142014
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20131051710.1002/anie.20131051710.1002/ange.201310517
first author openalex DuttwylerDuttwylerDuttwylerDuttwyler

Also recorded as

  • W4232543166 (DOI 10.1002/ange.201310517) · same title · 2014 Regio‐ and Stereoselective 1,2‐Dihydropyridine Alkylation/Addition Sequence for the Synthesis of Piperidines with Quaternary Centers

Citations

OpenAlex
60
Scholar
73
DOI
10.1002/anie.201310517
OpenAlex
W2131700791

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201310517 for regio- and stereoselective 1,2-dihydropyridine alkylation.
  • doi merged · 1.00 · Run 18
2013 Asymmetric Synthesis of Amines Using tert-Butanesulfinamide Nature Protocols article journal CV OA GS

CV span

lines 498–499 · CV · published

498104. Xu, H. C.; Chowdhury, S.; Ellman, J. A. “Asymmetric Synthesis of Amines Using tert-499Butanesulfinamide” Nat. Protoc. 8, 2271-2280 (2013).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, H. C.; Chowdhury, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Amines Using tert-ButanesulfinamideAsymmetric synthesis of amines using tert-butanesulfinamideAsymmetric synthesis of amines using tert-butanesulfinamide
year cv 201320132013
venue crossref Nat. Protoc.Nature ProtocolsNature protocolsNature Protocols
kind cv articlearticleother
DOI crossref 10.1038/nprot.2013.13410.1038/nprot.2013.134
first author openalex XuXuXu

Citations

OpenAlex
51
Scholar
59
DOI
10.1038/nprot.2013.134
OpenAlex
W2093414987

Match decisions

  • doi merged · 1.00 · Run 18
2013 Asymmetric Synthesis of α-Aminophosphonate Esters by the Addition of Dialkyl Phosphites to tert-Butanesulfinyl Imines Synthesis article journal CV OA GS

CV span

lines 501–502 · CV · published

501105. Khan, H, A.; Ellman, J.A. “Asymmetric Synthesis of α-Aminophosphonate Esters by the Addition502of Dialkyl Phosphites to tert-Butanesulfinyl Imines” Synthesis 45, 3147–3150 (2013).

Institution fields

Peer reviewed
yes
First author
Khan
Co-authors
Khan, H, A.; Ellman, J.A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Asymmetric Synthesis of α-Aminophosphonate Esters by the Addition of Dialkyl Phosphites to tert-Butanesulfinyl IminesAsymmetric Synthesis of α-Aminophosphonate Esters by the Addition of Dialkyl Phosphites to tert-Butanesulfinyl Imines
year cv 20132013
venue crossref SynthesisSynthesis
kind cv articlearticle
DOI crossref 10.1055/s-0033-133971210.1055/s-0033-1339712
first author openalex KhanEllman

Citations

OpenAlex
12
Scholar
none
DOI
10.1055/s-0033-1339712
OpenAlex
W2951100609

Match decisions

  • doi merged · 1.00 · Run 18
2013 Caspase inhibitors and uses thereof U.S. Patent No. 8,518,942 version 2016 Caspase inhibitors and uses thereof other CV OA GS

CV span

lines 1409–1410 · CV · published

14095. Ellerby; L. M.; Ellman; J. A.; Leyva; M. J. “Caspase inhibitors and uses thereof” U.S. (2013),1410Patent No. 8,518,942.

Institution fields

Peer reviewed
none
First author
Ellerby
Co-authors
Ellerby; L. M.; Ellman; J. A.; Leyva; M. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Caspase inhibitors and uses thereof
year cv 2013
venue cv U.S. Patent No. 8,518,942
kind cv other
first author cv Ellerby

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2013 Detection of Protease and Protease Activity Using a Single Nanoscrescent SERS Probe U.S. Patent No. 8,361,932 version 2015 Detection of Protease and Protease Activity Using a Single Nanoscrescent SERS Probe other CV OA GS

CV span

lines 1415–1417 · CV · published

14157. Liu, G. L.; Ellman, J. A.; Lee, L. P.; Chen, F. “Detection of Protease and Protease Activity Using a1416Single Nanoscrescent SERS Probe” U.S. (2013), Patent No. 8,361,932.1417

Institution fields

Peer reviewed
none
First author
Liu
Co-authors
Liu, G. L.; Ellman, J. A.; Lee, L. P.; Chen, F.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Detection of Protease and Protease Activity Using a Single Nanoscrescent SERS Probe
year cv 2013
venue cv U.S. Patent No. 8,361,932
kind cv other
first author cv Liu

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2013 Facile Synthesis of Unsymmetrical Acridines and Phenazines by a Rhodium(III)-Catalyzed Amination, Cyclization and Aromatization Cascade Journal of the American Chemical Society article journal CV OA GS

CV span

lines 494–496 · CV · published

494103. Lian, Y.; Hummel, J. R.; Bergman, R. G.; Ellman, J. A. “Facile Synthesis of Unsymmetrical495Acridines and Phenazines by a Rhodium(III)-Catalyzed Amination, Cyclization and Aromatization496Cascade” J. Am. Chem. Soc. 135, 12548–12551 (2013).

Institution fields

Peer reviewed
yes
First author
Lian
Co-authors
Lian, Y.; Hummel, J. R.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Facile Synthesis of Unsymmetrical Acridines and Phenazines by a Rhodium(III)-Catalyzed Amination, Cyclization and Aromatization CascadeFacile Synthesis of Unsymmetrical Acridines and Phenazines by a Rh(III)-Catalyzed Amination/Cyclization/Aromatization CascadeFacile Synthesis of Unsymmetrical Acridines and Phenazines by a Rhodium (III)-Catalyzed Amination, Cyclization and Aromatization Cascade
year cv 201320132013
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja406131a10.1021/ja406131a
first author openalex LianLianLian

Citations

OpenAlex
213
Scholar
227
DOI
10.1021/ja406131a
OpenAlex
W2322705312

Match decisions

  • doi merged · 1.00 · Run 18
2013 Mechanistic Study of the Oxidative Coupling of Styrene with 2-Phenylpyridine Derivatives Catalyzed by Cationic Rhodium(III) via C–H Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 507–509 · CV · published

507107. Brasse, M.; Cámpora, J.; Begman, R. G.; Ellman, J. A. “Mechanistic Study of the Oxidative508Coupling of Styrene with 2-Phenylpyridine Derivatives Catalyzed by Cationic Rhodium(III) via C–509H Activation” J. Am. Chem. Soc. 135, 6427–6430 (2013).

Institution fields

Peer reviewed
yes
First author
Brasse
Co-authors
Brasse, M.; Cámpora, J.; Begman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Mechanistic Study of the Oxidative Coupling of Styrene with 2-Phenylpyridine Derivatives Catalyzed by Cationic Rhodium(III) via C–H ActivationMechanistic Study of the Oxidative Coupling of Styrene with 2-Phenylpyridine Derivatives Catalyzed by Cationic Rhodium(III) via C–H ActivationMechanistic study of the oxidative coupling of styrene with 2-phenylpyridine derivatives catalyzed by cationic Rhodium (III) via C–H activation
year cv 201320132013
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja401561q10.1021/ja401561q
first author openalex BrasseBrasseBrasse

Citations

OpenAlex
92
Scholar
95
DOI
10.1021/ja401561q
OpenAlex
W2021709320

Match decisions

  • doi merged · 1.00 · Run 18
2013 Proton Donor Acidity Controls Selectivity in Nonaromatic Nitrogen Heterocycle Synthesis Science article journal CV OA GS

CV span

lines 515–517 · CV · published

515109. Duttwyler, S.; Chen, S.; Takase, M. K.; Wiberg, K. B.; Bergman, R. G.; Ellman, J. A. “Proton516Donor Acidity Controls Selectivity in Nonaromatic Nitrogen Heterocycle Synthesis” Science 339,517678-982 (2013) [News of the Week Chem & Eng News 91, issue 6, 7 (2013)].

Institution fields

Peer reviewed
yes
First author
Duttwyler
Co-authors
Duttwyler, S.; Chen, S.; Takase, M. K.; Wiberg, K. B.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Proton Donor Acidity Controls Selectivity in Nonaromatic Nitrogen Heterocycle SynthesisProton Donor Acidity Controls Selectivity in Nonaromatic Nitrogen Heterocycle SynthesisProton donor acidity controls selectivity in nonaromatic nitrogen heterocycle synthesis
year cv 201320132013
venue crossref ScienceScienceScience
kind cv articlearticleother
DOI crossref 10.1126/science.123070410.1126/science.1230704
first author openalex DuttwylerDuttwylerDuttwyler

Citations

OpenAlex
76
Scholar
84
DOI
10.1126/science.1230704
OpenAlex
W2018846002

Match decisions

  • doi merged · 1.00 · Run 18
2013 Rhodium(III)-Catalyzed Alkenyl C-H Bond Functionalization: Convergent Synthesis of Furans and Pyrroles Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 522–524 · CV · published

522111. Lian, Y.; Huber, T.; Hesp, K. D.; Bergman, R. G.; Ellman, J. A. “Rhodium(III)-Catalyzed Alkenyl523C-H Bond Functionalization: Convergent Synthesis of Furans and Pyrroles” Angew. Chem. Int. Ed.52452, 629-633 (2013).

Institution fields

Peer reviewed
yes
First author
Lian
Co-authors
Lian, Y.; Huber, T.; Hesp, K. D.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium(III)-Catalyzed Alkenyl C-H Bond Functionalization: Convergent Synthesis of Furans and PyrrolesRhodium(III)‐Catalyzed Alkenyl CH Bond Functionalization: Convergent Synthesis of Furans and PyrrolesRhodium(III)‐Catalyzed Alkenyl CH Bond Functionalization: Convergent Synthesis of Furans and PyrrolesRhodium (III)‐Catalyzed Alkenyl C H Bond Functionalization: Convergent Synthesis of Furans and Pyrroles
year cv 2013201220122013
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20120799510.1002/anie.20120799510.1002/ange.201207995
first author openalex LianLianLianLian

Also recorded as

  • W4249595705 (DOI 10.1002/ange.201207995) · platform twin · 2012 Rhodium(III)‐Catalyzed Alkenyl CH Bond Functionalization: Convergent Synthesis of Furans and Pyrroles

Citations

OpenAlex
179
Scholar
175
DOI
10.1002/anie.201207995
OpenAlex
W2110366390

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201207995 for rhodium(iii)-catalyzed alkenyl C-H bond functionalization.
  • doi merged · 1.00 · Run 18
2013 Rhodium(III)-Catalyzed Indazole Synthesis by C-H Bond Functionalization and Cyclative Capture Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 504–505 · CV · published

504106. Lian, Y.; Bergman, R. G.; Lavis, L. D.; Ellman, J. A. “Rhodium(III)-Catalyzed Indazole Synthesis505by C-H Bond Functionalization and Cyclative Capture” J. Am. Chem. Soc. 135, 7122-7125 (2013).

Institution fields

Peer reviewed
yes
First author
Lian
Co-authors
Lian, Y.; Bergman, R. G.; Lavis, L. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium(III)-Catalyzed Indazole Synthesis by C-H Bond Functionalization and Cyclative CaptureRhodium(III)-Catalyzed Indazole Synthesis by C–H Bond Functionalization and Cyclative CaptureRhodium (III)-catalyzed indazole synthesis by C–H bond functionalization and cyclative capture
year cv 201320132013
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja402761p10.1021/ja402761p
first author openalex LianLianLian

Citations

OpenAlex
312
Scholar
328
DOI
10.1021/ja402761p
OpenAlex
W2005832001

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201207995 for rhodium(iii)-catalyzed alkenyl C-H bond functionalization.
  • doi merged · 1.00 · Run 18
2013 Substrate-Based Fragment Identification for the Development of Selective, Nonpeptidic Inhibitors of Striatal-Enriched Protein Tyrosine Phophatase Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 490–492 · CV · published

490102. Baguley, T. D.; Xu, H.-C.; Chatterjee, M.; Nairn, A. C.; Lombroso, P. J.; Ellman, J. A. “Substrate-491Based Fragment Identification for the Development of Selective, Nonpeptidic Inhibitors of Striatal-492Enriched Protein Tyrosine Phophatase” J. Med. Chem. 56, 7636-7650 (2013).

Institution fields

Peer reviewed
yes
First author
Baguley
Co-authors
Baguley, T. D.; Xu, H.-C.; Chatterjee, M.; Nairn, A. C.; Lombroso, P. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Substrate-Based Fragment Identification for the Development of Selective, Nonpeptidic Inhibitors of Striatal-Enriched Protein Tyrosine PhophataseSubstrate-Based Fragment Identification for the Development of Selective, Nonpeptidic Inhibitors of Striatal-Enriched Protein Tyrosine PhosphataseSubstrate-based fragment identification for the development of selective, nonpeptidic inhibitors of striatal-enriched protein tyrosine phosphatase
year cv 201320132013
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm401037h10.1021/jm401037h
first author openalex BaguleyBaguleyBaguley

Citations

OpenAlex
35
Scholar
44
DOI
10.1021/jm401037h
OpenAlex
W2076031215

Match decisions

  • doi merged · 1.00 · Run 18
2013 Synthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels-Alder Reaction Organic Letters article journal CV OA GS needs review

CV span

lines 519–520 · CV · published

519110. Martin, R. M.; Bergman, R. G.; Ellman, J. A. “Synthesis of Isoquinuclidines from Highly520Substituted Dihydropyridines via the Diels-Alder Reaction” Org. Lett. 15, 444-447 (2013).

Institution fields

Peer reviewed
yes
First author
Martin
Co-authors
Martin, R. M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels-Alder ReactionSynthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels–Alder ReactionSynthesis of isoquinuclidines from highly substituted dihydropyridines via the Diels-Alder reaction
year cv 201320132013
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol303040r10.1021/ol303040r
first author openalex MartinMartinMartin

Citations

OpenAlex
52
Scholar
57
DOI
10.1021/ol303040r
OpenAlex
W1982910646

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol303040r for synthesis of isoquinuclidines.
  • doi merged · 1.00 · Run 18
2013 Tubulysin D Analogues U.S. Patent No. 8,476,451 other CV OA GS

CV span

lines 1412–1413 · CV · published

14126. Ellman, J. A.; Patterson, A. W.; Peltier, H. “Tubulysin D Analogues” U.S. (2013), Patent No.14138,476,451.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J. A.; Patterson, A. W.; Peltier, H.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Tubulysin D AnaloguesTubulysin D analogues
year cv 20132013
venue cv U.S. Patent No. 8,476,451US Patent
kind cv otherother
first author cv EllmanEllman

Citations

OpenAlex
none
Scholar
45

Match decisions

  • fingerprint merged · 1.00 · Run 18
2013 Unstabilized Azomethine Ylides for the Stereoselective synthesis of Substituted Piperidines, Tropanes and Azabicyclo[3.1.0] systems Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 511–513 · CV · published

511108. Ischay, M. A.; Takase, M. K.; Bergman, R. G.; Ellman, J. A. “Unstabilized Azomethine Ylides for512the Stereoselective synthesis of Substituted Piperidines, Tropanes and Azabicyclo[3.1.0] systems”513J. Am. Chem. Soc. 135, 2478–2481 (2013) [JACS Spotlight highlighted by the Editors].

Institution fields

Peer reviewed
yes
First author
Ischay
Co-authors
Ischay, M. A.; Takase, M. K.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Unstabilized Azomethine Ylides for the Stereoselective synthesis of Substituted Piperidines, Tropanes and Azabicyclo[3.1.0] systemsUnstabilized Azomethine Ylides for the Stereoselective Synthesis of Substituted Piperidines, Tropanes, and Azabicyclo[3.1.0] SystemsUnstabilized azomethine ylides for the stereoselective synthesis of substituted piperidines, tropanes and azabicyclo [3.1. 0] systems
year cv 201320132013
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja312311k10.1021/ja312311k
first author openalex IschayIschayIschay

Citations

OpenAlex
56
Scholar
61
DOI
10.1021/ja312311k
OpenAlex
W1974195686

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja312311k for unstabilized azomethine ylides.
  • doi merged · 1.00 · Run 18
2012 A Nonpeptidic Cathepsin S Activity-Based Probe for Noninvasive Optical Imaging of Tumor-Associated Macrophages Chemistry & Biology article journal CV OA GS

CV span

lines 533–535 · CV · published

533114. Verdoes, M.; Edgington, L. E.; Scheeren, F. A.; Leyva, M.; Blum, G.; Weiskopf, K.; Bachmann, M.534H.; Ellman, J. A.; Bogyo, M. “A Nonpeptidic Cathepsin S Activity-Based Probe for Noninvasive535Optical Imaging of Tumor-Associated Macrophages” Chem. Biol. 19, 619–628 (2012).

Institution fields

Peer reviewed
yes
First author
Verdoes
Co-authors
Verdoes, M.; Edgington, L. E.; Scheeren, F. A.; Leyva, M.; Blum, G.; Weiskopf, K.; Bachmann, M. H.; Ellman, J. A.; Bogyo, M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Nonpeptidic Cathepsin S Activity-Based Probe for Noninvasive Optical Imaging of Tumor-Associated MacrophagesA Nonpeptidic Cathepsin S Activity-Based Probe for Noninvasive Optical Imaging of Tumor-Associated MacrophagesA nonpeptidic cathepsin S activity-based probe for noninvasive optical imaging of tumor-associated macrophages
year cv 201220122012
venue crossref Chem. Biol.Chemistry & BiologyChemistry & biologyChemistry & Biology
kind cv articlearticleother
DOI crossref 10.1016/j.chembiol.2012.03.01210.1016/j.chembiol.2012.03.012
first author openalex VerdoesVerdoesVerdoes

Citations

OpenAlex
113
Scholar
130
DOI
10.1016/j.chembiol.2012.03.012
OpenAlex
W2053051636

Match decisions

  • doi merged · 1.00 · Run 18
2012 Catalytic Enantioselective Protonation of Nitronates Utilizing an Organocatalyst Chiral Only at Sulfur Journal of the American Chemical Society article journal CV OA GS

CV span

lines 537–539 · CV · published

537115. Kimmel, K. K.; Weaver, J. D.; Lee, M.; Ellman, J. A. “Catalytic Enantioselective Protonation of538Nitronates Utilizing an Organocatalyst Chiral Only at Sulfur” J. Am. Chem. Soc. 134, 9058–9061539(2012).

Institution fields

Peer reviewed
yes
First author
Kimmel
Co-authors
Kimmel, K. K.; Weaver, J. D.; Lee, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Protonation of Nitronates Utilizing an Organocatalyst Chiral Only at SulfurCatalytic Enantioselective Protonation of Nitronates Utilizing an Organocatalyst Chiral Only at SulfurCatalytic enantioselective protonation of nitronates utilizing an organocatalyst chiral only at sulfur
year cv 201220122012
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja302619610.1021/ja3026196
first author openalex KimmelKimmelKimmel

Citations

OpenAlex
84
Scholar
99
DOI
10.1021/ja3026196
OpenAlex
W2321680965

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: excluded
2012 Conformational Change in Rhomboid Protease GlpG Induced by Inhibitor Binding to Its S′ Subsites Biochemistry article journal CV OA GS

CV span

lines 541–543 · CV · published

541116. Xue, Y.; Chowdhury, S.; Liu, X.; Akiyama, Y.; Ellman, J. A.; Ha, Y. “Conformational Change in542Rhomboid Protease GlpG Induced by Inhibitor Binding to Its S′ Subsites” Biochemistry 51, 3723–5433731 (2012).

Institution fields

Peer reviewed
yes
First author
Xue
Co-authors
Xue, Y.; Chowdhury, S.; Liu, X.; Akiyama, Y.; Ellman, J. A.; Ha, Y.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Conformational Change in Rhomboid Protease GlpG Induced by Inhibitor Binding to Its S′ SubsitesConformational Change in Rhomboid Protease GlpG Induced by Inhibitor Binding to Its S′ SubsitesThe conformational change in rhomboid protease GlpG induced by inhibitor binding to its S’-subsites
year cv 201220122012
venue crossref BiochemistryBiochemistryBiochemistry
kind cv articlearticleother
DOI crossref 10.1021/bi300368b10.1021/bi300368b
first author openalex XueXueXue

Citations

OpenAlex
53
Scholar
67
DOI
10.1021/bi300368b
OpenAlex
W1990205832

Match decisions

  • doi merged · 1.00 · Run 18
2012 Enantio- and Diastereoselective Addition of Cyclohexyl Meldrum’s Acid to β- and α,β-Disubstituted Nitroalkenes via N-Sulfinyl Urea Catalysis ChemInform article journal CV OA GS needs review

CV span

lines 566–568 · CV · published

566123. Kimmel, K. K.; Weaver, J. D.; Ellman, J. A. “Enantio- and Diastereoselective Addition of567Cyclohexyl Meldrum’s Acid to β- and α,β-Disubstituted Nitroalkenes via N-Sulfinyl Urea568Catalysis” Chem. Sci. 3, 121-125 (2012).

Institution fields

Peer reviewed
yes
First author
Kimmel
Co-authors
Kimmel, K. K.; Weaver, J. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantio- and Diastereoselective Addition of Cyclohexyl Meldrum’s Acid to β- and α,β-Disubstituted Nitroalkenes via N-Sulfinyl Urea CatalysisChemInform Abstract: Enantio‐ and Diastereoselective Addition of Thioacetic Acid to Nitroalkenes via N‐Sulfinyl Urea Catalysis.ChemInform Abstract: Rhodium(III)‐Catalyzed Indazole Synthesis by C—H Bond Functionalization and Cyclative Capture.ChemInform Abstract: Rh‐Catalyzed Addition of Arylboroxines to Cyclic N‐(Isopropanesulfinyl)ketimines.ChemInform Abstract: Synthesis of Pyridines from Ketoximes and Terminal Alkynes via C—H Bond Functionalization.ChemInform Abstract: Unstabilized Azomethine Ylides for the Stereoselective Synthesis of Substituted Piperidines, Tropanes, and Azabicyclo[3.1.0] Systems.ChemInform Abstract: Catalytic C—O Bond Cleavage of 2‐Aryloxy‐1‐arylethanols and Its Application to the Depolymerization of Lignin‐Related Polymers.ChemInform Abstract: Enantio‐ and Diastereoselective Addition of Cyclohexyl Meldrum′s Acid to β‐ and α,β‐Disubstituted Nitroalkenes via N‐Sulfinyl Urea Catalysis.ChemInform Abstract: Asymmetric Synthesis of Amines by the Knochel‐Type MgCl2‐Enhanced Addition of Benzyl Zinc Reagents to N‐tert‐Butanesulfinyl Aldimines.ChemInform Abstract: Development of an N‐Sulfinyl Prolinamide for the Asymmetric Aldol Reaction.ChemInform Abstract: Rh(I)‐Catalyzed Direct Arylation of Azines.ChemInform Abstract: Expedient Synthesis of N‐Acyl Anthranilamides and β‐Enamine Amides by the Rh(III)‐Catalyzed Amidation of Aryl and Vinylic C—H Bonds with Isocyanates.ChemInform Abstract: Rh(III)‐Catalyzed Oxidative Coupling of Unactivated Alkenes via C—H Activation.ChemInform Abstract: A Facile, Metal‐ and Solvent‐Free, Autoxidative Coupling of Quinolines with Indoles and Pyrroles.ChemInform Abstract: Rhodium(III)‐Catalyzed Arylation of Boc‐Imines via C—H Bond Functionalization.ChemInform Abstract: Synthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels—Alder Reaction.ChemInform Abstract: Rhodium(III)‐Catalyzed Synthesis of Phthalides by Cascade Addition and Cyclization of Benzimidates with Aldehydes.ChemInform Abstract: Rhodium(III)‐Catalyzed Alkenyl C—H Bond Functionalization: Convergent Synthesis of Furans and Pyrroles.ChemInform Abstract: Highly Functional Group Compatible Rh‐Catalyzed Addition of Arylboroxines to Activated N‐tert‐Butanesulfinyl Ketimines.ChemInform Abstract: Rhodium‐Catalyzed Synthesis of Branched Amines by Direct Addition of Benzamides to Imines.ChemInform Abstract: Highly Diastereoselective Synthesis of Tetrahydropyridines by a C—H Activation—Cyclization—Reduction Cascade.Enantio- and diastereoselective addition of cyclohexyl Meldrum's acid to β- and α,β-disubstituted nitroalkenesvia N-sulfinyl urea catalysis
year cv 2012201220132013201220132011201220112011201120112011201120112013201320132011201220122011
venue crossref Chem. Sci.ChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemical ScienceChemInform
kind cv articlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticlearticleother
DOI crossref 10.1002/chin.20121807810.1002/chin.20123010810.1002/chin.20134411610.1002/chin.20131115110.1002/chin.20122714910.1002/chin.20133003410.1002/chin.20110603210.1002/chin.20121807810.1002/chin.20112305710.1002/chin.20114306010.1002/chin.20111015110.1002/chin.20115203810.1002/chin.20111709910.1002/chin.20113414710.1002/chin.20113106910.1002/chin.20132414610.1002/chin.20131109710.1002/chin.20132003810.1002/chin.20115007610.1002/chin.20123505110.1002/chin.201231153
first author openalex KimmelKimmelLianJungMartinIschayNicholsKimmelBueskingRobakBermanHespTsaiBrasseTsaiMartinLianLianJungHespDuttwylerKimmel

Also recorded as

  • W2018843530 (DOI 10.1002/chin.201230108) · platform twin · 2012 ChemInform Abstract: Enantio‐ and Diastereoselective Addition of Thioacetic Acid to Nitroalkenes via N‐Sulfinyl Urea Catalysis.
  • W2950021719 (DOI 10.1002/chin.201344116) · platform twin · 2013 ChemInform Abstract: Rhodium(III)‐Catalyzed Indazole Synthesis by C—H Bond Functionalization and Cyclative Capture.
  • W2950024569 (DOI 10.1002/chin.201311151) · platform twin · 2013 ChemInform Abstract: Rh‐Catalyzed Addition of Arylboroxines to Cyclic N‐(Isopropanesulfinyl)ketimines.
  • W2950064024 (DOI 10.1002/chin.201227149) · platform twin · 2012 ChemInform Abstract: Synthesis of Pyridines from Ketoximes and Terminal Alkynes via C—H Bond Functionalization.
  • W2950082335 (DOI 10.1002/chin.201330034) · platform twin · 2013 ChemInform Abstract: Unstabilized Azomethine Ylides for the Stereoselective Synthesis of Substituted Piperidines, Tropanes, and Azabicyclo[3.1.0] Systems.
  • W2950105840 (DOI 10.1002/chin.201106032) · platform twin · 2011 ChemInform Abstract: Catalytic C—O Bond Cleavage of 2‐Aryloxy‐1‐arylethanols and Its Application to the Depolymerization of Lignin‐Related Polymers.
  • W2950714620 (DOI 10.1002/chin.201123057) · platform twin · 2011 ChemInform Abstract: Asymmetric Synthesis of Amines by the Knochel‐Type MgCl2‐Enhanced Addition of Benzyl Zinc Reagents to N‐tert‐Butanesulfinyl Aldimines.
  • W2950773916 (DOI 10.1002/chin.201143060) · platform twin · 2011 ChemInform Abstract: Development of an N‐Sulfinyl Prolinamide for the Asymmetric Aldol Reaction.
  • W2950840243 (DOI 10.1002/chin.201110151) · platform twin · 2011 ChemInform Abstract: Rh(I)‐Catalyzed Direct Arylation of Azines.
  • W2951210300 (DOI 10.1002/chin.201152038) · platform twin · 2011 ChemInform Abstract: Expedient Synthesis of N‐Acyl Anthranilamides and β‐Enamine Amides by the Rh(III)‐Catalyzed Amidation of Aryl and Vinylic C—H Bonds with Isocyanates.
  • W2951260361 (DOI 10.1002/chin.201117099) · platform twin · 2011 ChemInform Abstract: Rh(III)‐Catalyzed Oxidative Coupling of Unactivated Alkenes via C—H Activation.
  • W2951468065 (DOI 10.1002/chin.201134147) · platform twin · 2011 ChemInform Abstract: A Facile, Metal‐ and Solvent‐Free, Autoxidative Coupling of Quinolines with Indoles and Pyrroles.
  • W2952062794 (DOI 10.1002/chin.201131069) · platform twin · 2011 ChemInform Abstract: Rhodium(III)‐Catalyzed Arylation of Boc‐Imines via C—H Bond Functionalization.
  • W2952151150 (DOI 10.1002/chin.201324146) · platform twin · 2013 ChemInform Abstract: Synthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels—Alder Reaction.
  • W2952440418 (DOI 10.1002/chin.201311097) · platform twin · 2013 ChemInform Abstract: Rhodium(III)‐Catalyzed Synthesis of Phthalides by Cascade Addition and Cyclization of Benzimidates with Aldehydes.
  • W2952464050 (DOI 10.1002/chin.201320038) · platform twin · 2013 ChemInform Abstract: Rhodium(III)‐Catalyzed Alkenyl C—H Bond Functionalization: Convergent Synthesis of Furans and Pyrroles.
  • W2952531843 (DOI 10.1002/chin.201150076) · platform twin · 2011 ChemInform Abstract: Highly Functional Group Compatible Rh‐Catalyzed Addition of Arylboroxines to Activated N‐tert‐Butanesulfinyl Ketimines.
  • W2952794741 (DOI 10.1002/chin.201235051) · platform twin · 2012 ChemInform Abstract: Rhodium‐Catalyzed Synthesis of Branched Amines by Direct Addition of Benzamides to Imines.
  • W2953135856 (DOI 10.1002/chin.201231153) · platform twin · 2012 ChemInform Abstract: Highly Diastereoselective Synthesis of Tetrahydropyridines by a C—H Activation—Cyclization—Reduction Cascade.

Citations

OpenAlex
0
Scholar
71
DOI
10.1002/chin.201218078
OpenAlex
W2950164562

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja203495c for expedient synthesis of N-acyl anthranilamides.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo202280e for synthesis of pyridines from ketoximes.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol102890k for rh(iii)-catalyzed oxidative coupling.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol300723x for rhodium-catalyzed synthesis of branched amines.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja2119833 for highly diastereoselective synthesis of tetrahydropyridines.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/j.tet.2011.03.030 for N-sulfinyl prolinamide.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol103002t for knochel-type addition of benzyl zinc reagents.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/j.tet.2012.01.048 for thioacetic acid addition to nitroalkenes.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja312311k for unstabilized azomethine ylides.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201207995 for rhodium(iii)-catalyzed alkenyl C-H bond functionalization.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1039/c1cc10507h for autoxidative coupling of quinolines.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol201438k for rh-catalyzed addition of arylboroxines.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol303040r for synthesis of isoquinuclidines.
  • doi merged · 1.00 · Run 18
2012 Enantio- and Diastereoselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea Catalysis Tetrahedron article journal CV OA GS needs review

CV span

lines 556–558 · CV · published

556120. Kimmel, K. K.; Robak, M. T.; Thomas, S.; Lee, M.; Ellman, J. A. “Enantio- and Diastereoselective557Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea Catalysis” Tetrahedron 68, 2704-5582712 (2012).

Institution fields

Peer reviewed
yes
First author
Kimmel
Co-authors
Kimmel, K. K.; Robak, M. T.; Thomas, S.; Lee, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Enantio- and Diastereoselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea CatalysisEnantio- and diastereoselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea catalysisEnantio-and diastereoselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea catalysis
year cv 201220122012
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/j.tet.2012.01.04810.1016/j.tet.2012.01.048
first author openalex KimmelKimmelKimmel

Citations

OpenAlex
37
Scholar
45
DOI
10.1016/j.tet.2012.01.048
OpenAlex
W2950603495

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/j.tet.2012.01.048 for thioacetic acid addition to nitroalkenes.
  • doi merged · 1.00 · Run 18
2012 Highly Diastereoselective Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction Cascade Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 548–550 · CV · published

548118. Duttwyler, S.; Rheingold, A. L.; Bergman, R. G.; Ellman, J. A. “Highly Diastereoselective549Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction Cascade” J. Am.550Chem. Soc. 134, 4064-4067 (2012).

Institution fields

Peer reviewed
yes
First author
Duttwyler
Co-authors
Duttwyler, S.; Rheingold, A. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Diastereoselective Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction CascadeHighly Diastereoselective Synthesis of Tetrahydropyridines by a C–H Activation–Cyclization–Reduction CascadeHighly diastereoselective synthesis of tetrahydropyridines by a C–H activation–cyclization–reduction cascade
year cv 201220122012
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja211983310.1021/ja2119833
first author openalex DuttwylerDuttwylerDuttwyler

Citations

OpenAlex
131
Scholar
141
DOI
10.1021/ja2119833
OpenAlex
W2085247175

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja2119833 for highly diastereoselective synthesis of tetrahydropyridines.
  • doi merged · 1.00 · Run 18
2012 Mechanism of the Rhodium(III)-Catalyzed Arylation of Imines via C–H Bond Functionalization: Inhibition by Substrate Journal of the American Chemical Society article journal CV OA GS

CV span

lines 552–554 · CV · published

552119. Tauchert, M. E.; Incarvito, C. D.; Rheingold, A. L.; Bergman, R. G.; Ellman, J. A. “Mechanism of553the Rhodium(III)-Catalyzed Arylation of Imines via C–H Bond Functionalization: Inhibition by554Substrate” J. Am. Chem. Soc. 134, 1482–1485 (2012).

Institution fields

Peer reviewed
yes
First author
Tauchert
Co-authors
Tauchert, M. E.; Incarvito, C. D.; Rheingold, A. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Mechanism of the Rhodium(III)-Catalyzed Arylation of Imines via C–H Bond Functionalization: Inhibition by SubstrateMechanism of the Rhodium(III)-Catalyzed Arylation of Imines via C–H Bond Functionalization: Inhibition by SubstrateMechanism of the rhodium (III)-catalyzed arylation of imines via C–H bond functionalization: inhibition by substrate
year cv 201220122012
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja211110h10.1021/ja211110h
first author openalex TauchertTauchertTauchert

Citations

OpenAlex
178
Scholar
185
DOI
10.1021/ja211110h
OpenAlex
W2033830818

Match decisions

  • doi merged · 1.00 · Run 18
2012 Rh-Catalyzed Addition of Arylboroxines to Cyclic N-(Isopropanesulfinyl)ketimines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 526–527 · CV · published

526112. Jung, H. H.; Buesking, A. W.; Ellman, J. A. “Rh-Catalyzed Addition of Arylboroxines to Cyclic N-527(Isopropanesulfinyl)ketimines” J. Org. Chem. 77, 9593-9600 (2012).

Institution fields

Peer reviewed
yes
First author
Jung
Co-authors
Jung, H. H.; Buesking, A. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh-Catalyzed Addition of Arylboroxines to Cyclic N-(Isopropanesulfinyl)ketiminesRh-Catalyzed Addition of Arylboroxines to Cyclic N-(Isopropanesulfinyl)ketimines
year cv 20122012
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/jo301634y10.1021/jo301634y
first author openalex JungJung

Citations

OpenAlex
10
Scholar
none
DOI
10.1021/jo301634y
OpenAlex
W2335550604

Match decisions

  • doi merged · 1.00 · Run 18
2012 Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization Reactions Accounts of Chemical Research article journal CV OA GS

CV span

lines 560–561 · CV · published

560121. Colby, D. A.; Tsai, A. S.; Bergman, R. G.; Ellman, J. A. “Rhodium Catalyzed Chelation-Assisted561C–H Bond Functionalization Reactions” Acc. Chem. Res. 45, 814–825 (2012).

Institution fields

Peer reviewed
yes
First author
Colby
Co-authors
Colby, D. A.; Tsai, A. S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization ReactionsRhodium Catalyzed Chelation-Assisted C–H Bond Functionalization ReactionsRhodium catalyzed chelation-assisted C–H bond functionalization reactions
year cv 201220112012
venue crossref Acc. Chem. Res.Accounts of Chemical ResearchAccounts of Chemical ResearchAccounts of Chemical Research
kind cv articlearticleother
DOI crossref 10.1021/ar200190g10.1021/ar200190g
first author openalex ColbyColbyColby

Citations

OpenAlex
1400
Scholar
1491
DOI
10.1021/ar200190g
OpenAlex
W2036044855

Match decisions

  • doi merged · 1.00 · Run 18
2012 Rhodium-Catalyzed Synthesis of Branched Amines by Direct Addition of Benzamides to Imines Organic Letters article journal CV OA GS needs review

CV span

lines 545–547 · CV · published

545117. Hesp, K. D.; Bergman, R. G.; Ellman, J. A. “Rhodium-Catalyzed Synthesis of Branched Amines by546Direct Addition of Benzamides to Imines” Org. Lett. 14, 2304-2307 (2012).547

Institution fields

Peer reviewed
yes
First author
Hesp
Co-authors
Hesp, K. D.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed Synthesis of Branched Amines by Direct Addition of Benzamides to IminesRhodium-Catalyzed Synthesis of Branched Amines by Direct Addition of Benzamides to IminesRhodium-catalyzed synthesis of branched amines by direct addition of benzamides to imines
year cv 201220122012
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol300723x10.1021/ol300723x
first author openalex HespHespHesp

Citations

OpenAlex
103
Scholar
108
DOI
10.1021/ol300723x
OpenAlex
W2082138895

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol300723x for rhodium-catalyzed synthesis of branched amines.
  • doi merged · 1.00 · Run 18
2012 Rhodium(III)-Catalyzed Synthesis of Phthalides by Cascade Addition and Cyclization of Benzimidates with Aldehydes Chemical Science article journal CV OA GS

CV span

lines 529–531 · CV · published

529113. Lian, Y.; Bergman, R. G.; Ellman, J. A. “Rhodium(III)-Catalyzed Synthesis of Phthalides by530Cascade Addition and Cyclization of Benzimidates with Aldehydes” Chem. Sci. 3, 3088-3092531(2012).

Institution fields

Peer reviewed
yes
First author
Lian
Co-authors
Lian, Y.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium(III)-Catalyzed Synthesis of Phthalides by Cascade Addition and Cyclization of Benzimidates with AldehydesRhodium(iii)-catalyzed synthesis of phthalides by cascade addition and cyclization of benzimidates with aldehydesRhodium (III)-catalyzed synthesis of phthalides by cascade addition and cyclization of benzimidates with aldehydes
year cv 201220122012
venue crossref Chem. Sci.Chemical ScienceChemical scienceChemical Science
kind cv articlearticleother
DOI crossref 10.1039/c2sc20835k10.1039/c2sc20835k
first author openalex LianLianLian

Citations

OpenAlex
110
Scholar
105
DOI
10.1039/c2sc20835k
OpenAlex
W1976309739

Match decisions

  • doi merged · 1.00 · Run 18
2012 Synthesis of Pyridines from Ketoximes and Terminal Alkynes via C–H Bond Functionalization The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 563–564 · CV · published

563122. Martin, R. A.; Bergman, R. G.; Ellman, J. A. “Synthesis of Pyridines from Ketoximes and Terminal564Alkynes via C–H Bond Functionalization” J. Org. Chem. 77, 2501-2507 (2012).

Institution fields

Peer reviewed
yes
First author
Martin
Co-authors
Martin, R. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Pyridines from Ketoximes and Terminal Alkynes via C–H Bond FunctionalizationSynthesis of Pyridines from Ketoximes and Terminal Alkynes via C–H Bond FunctionalizationSynthesis of Pyridines from Ketoximes and Terminal Alkynes via C–H Bond Functionalization
year cv 201220122012
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo202280e10.1021/jo202280e
first author openalex MartinMartinMartin

Citations

OpenAlex
149
Scholar
156
DOI
10.1021/jo202280e
OpenAlex
W2326238162

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo202280e for synthesis of pyridines from ketoximes.
  • doi merged · 1.00 · Run 18
2011 A Facile, Metal- and Solvent Free, Autoxidative Coupling of Quinolines with Indoles and Pyrroles Chemical Communications article journal CV OA GS needs review

CV span

lines 582–583 · CV · published

582127. Brasse, M.; Ellman, J. A.; Bergman, R. G. “A Facile, Metal- and Solvent Free, Autoxidative583Coupling of Quinolines with Indoles and Pyrroles” Chem. Commun. 47, 5019-5021 (2011).

Institution fields

Peer reviewed
yes
First author
Brasse
Co-authors
Brasse, M.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Facile, Metal- and Solvent Free, Autoxidative Coupling of Quinolines with Indoles and PyrrolesA facile, metal- and solvent-free, autoxidative coupling of quinolines with indoles and pyrrolesA facile, metal-and solvent-free, autoxidative coupling of quinolines with indoles and pyrroles
year cv 201120112011
venue crossref Chem. Commun.Chemical CommunicationsChemical CommunicationsChemical Communications
kind cv articlearticleother
DOI crossref 10.1039/c1cc10507h10.1039/c1cc10507h
first author openalex BrasseBrasseBrasse

Citations

OpenAlex
52
Scholar
51
DOI
10.1039/c1cc10507h
OpenAlex
W2163464234

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1039/c1cc10507h for autoxidative coupling of quinolines.
  • doi merged · 1.00 · Run 18
2011 A Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to the Malaria Parasite ChemMedChem article journal CV OA GS

CV span

lines 585–587 · CV · published

585128. Mahajan, S. S.; Deu, E.; Lauterwasser, E. M. W.; Leyva, M. J.; Ellman, J. A.; Bogyo, M.; Renslo,586A. R. “A Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to587the Malaria Parasite” ChemMedChem 6, 415–419 (2011).

Institution fields

Peer reviewed
yes
First author
Mahajan
Co-authors
Mahajan, S. S.; Deu, E.; Lauterwasser, E. M. W.; Leyva, M. J.; Ellman, J. A.; Bogyo, M.; Renslo, A. R.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv A Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to the Malaria ParasiteA Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to the Malaria ParasiteInside Cover: A Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to the Malaria Parasite (ChemMedChem 3/2011)A fragmenting hybrid approach for targeted delivery of multiple therapeutic agents to the malaria parasite
year cv 2011201120112011
venue crossref ChemMedChemChemMedChemChemMedChemChemMedChem
kind cv articlearticlearticleother
DOI crossref 10.1002/cmdc.20110000210.1002/cmdc.20110000210.1002/cmdc.201190006
first author openalex MahajanMahajanMahajanMahajan

Also recorded as

  • W2129731710 (DOI 10.1002/cmdc.201190006) · title variant · 2011 Inside Cover: A Fragmenting Hybrid Approach for Targeted Delivery of Multiple Therapeutic Agents to the Malaria Parasite (ChemMedChem 3/2011)

Citations

OpenAlex
31
Scholar
33
DOI
10.1002/cmdc.201100002
OpenAlex
W2063077062

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: title_variant
2011 Asymmetric Synthesis of Amines by the Knochel-Type MgCl2-Enhanced Addition of Benzyl Zinc Reagents to N-tert-Butanesulfinyl Aldimines Organic Letters article journal CV OA GS needs review

CV span

lines 589–591 · CV · published

589129. Buesking, A. W.; Baguley, T. D.; Ellman, J. A. “Asymmetric Synthesis of Amines by the Knochel-590Type MgCl2-Enhanced Addition of Benzyl Zinc Reagents to N-tert-Butanesulfinyl Aldimines” Org.591Lett. 13, 964-967 (2011).

Institution fields

Peer reviewed
yes
First author
Buesking
Co-authors
Buesking, A. W.; Baguley, T. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Amines by the Knochel-Type MgCl2-Enhanced Addition of Benzyl Zinc Reagents to N-tert-Butanesulfinyl AldiminesAsymmetric Synthesis of Amines by the Knochel-Type MgCl 2 -Enhanced Addition of Benzyl Zinc Reagents to N - tert -Butanesulfinyl AldiminesAsymmetric Synthesis of Amines by the Knochel-Type MgCl2-Enhanced Addition of Benzyl Zinc Reagents to N-tert-Butanesulfinyl Aldimines
year cv 201120112011
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol103002t10.1021/ol103002t
first author openalex BueskingBueskingBuesking

Citations

OpenAlex
34
Scholar
43
DOI
10.1021/ol103002t
OpenAlex
W2104230074

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol103002t for knochel-type addition of benzyl zinc reagents.
  • doi merged · 1.00 · Run 18
2011 Catalytic disproportionation and catalytic reduction of carbon-carbon and carbon-oxygen bonds of lignin and other organic substrate PCT Int. Appl. other CV OA GS

CV span

lines 1469–1472 · CV · published

14695. Bergman, R.; Ellman, J.; Nichols, J.; Bishop, L.; Volkman, J.; Toste, D.; Son, S.; Hartwig, J.;1470Sergeev, A. "Catalytic disproportionation and catalytic reduction of carbon-carbon and carbon-1471oxygen bonds of lignin and other organic substrate” PCT Int. Appl. (2011),1472WO 2011003029 A2 20110106.

Institution fields

Peer reviewed
none
First author
Bergman
Co-authors
Bergman, R.; Ellman, J.; Nichols, J.; Bishop, L.; Volkman, J.; Toste, D.; Son, S.; Hartwig, J.; Sergeev, A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Catalytic disproportionation and catalytic reduction of carbon-carbon and carbon-oxygen bonds of lignin and other organic substrate
year cv 2011
venue cv PCT Int. Appl.
kind cv other
first author cv Bergman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2011 Chemotherapeutic Evaluation of a Novel Synthetic Tubulysin Analogue-Dendrimer Conjugate in C26 Tumor Bearing Mice ChemMedChem article journal CV OA GS

CV span

lines 600–603 · CV · published

600132. Floyd III, W. C.; Datta, G. K.; Imamura, S.; Kieler-Ferguson, H. M.; Jerger, K.; Patterson, A. W.;601Fox, M. E.; Szoka, F. C.; Fréchet, J. M. J.; Ellman, J. A. “Chemotherapeutic Evaluation of a Novel602Synthetic Tubulysin Analogue-Dendrimer Conjugate in C26 Tumor Bearing Mice” ChemMedChem6036, 49-53 (2011) [selected as Very Important Paper].

Institution fields

Peer reviewed
yes
First author
Floyd III
Co-authors
Floyd III, W. C.; Datta, G. K.; Imamura, S.; Kieler-Ferguson, H. M.; Jerger, K.; Patterson, A. W.; Fox, M. E.; Szoka, F. C.; Fréchet, J. M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Chemotherapeutic Evaluation of a Novel Synthetic Tubulysin Analogue-Dendrimer Conjugate in C26 Tumor Bearing MiceChemotherapeutic Evaluation of a Synthetic Tubulysin Analogue–Dendrimer Conjugate in C26 Tumor Bearing MiceChemotherapeutic evaluation of a synthetic tubulysin analogue–dendrimer conjugate in c26 tumor bearing mice
year cv 201120102011
venue crossref ChemMedChemChemMedChemChemMedChem
kind cv articlearticleother
DOI crossref 10.1002/cmdc.20100037710.1002/cmdc.201000377
first author openalex FloydFloydFloyd

Citations

OpenAlex
33
Scholar
44
DOI
10.1002/cmdc.201000377
OpenAlex
W2063512846

Match decisions

  • doi merged · 1.00 · Run 18
2011 Development of an N-Sulfinyl Prolinamide for the Asymmetric Aldol Reaction Tetrahedron article journal CV OA GS needs review

CV span

lines 578–580 · CV · published

578126. Robak, M. T.; Herbage, M. A.; Ellman, J. A. “Development of an N-Sulfinyl Prolinamide for the579Asymmetric Aldol Reaction” Tetrahedron, 67, 4412-4416 (2011) [Dean Toste Tetrahedron Young580Investigator Award Issue].

Institution fields

Peer reviewed
yes
First author
Robak
Co-authors
Robak, M. T.; Herbage, M. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Development of an N-Sulfinyl Prolinamide for the Asymmetric Aldol ReactionDevelopment of an N-sulfinyl prolinamide for the asymmetric aldol reactionDevelopment of an N-sulfinyl prolinamide for the asymmetric aldol reaction
year cv 201120112011
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/j.tet.2011.03.03010.1016/j.tet.2011.03.030
first author openalex RobakRobakRobak

Citations

OpenAlex
39
Scholar
53
DOI
10.1016/j.tet.2011.03.030
OpenAlex
W1968859279

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/j.tet.2011.03.030 for N-sulfinyl prolinamide.
  • doi merged · 1.00 · Run 18
2011 Expedient Synthesis of N-Acyl Anthranilamides and β-Enamine Amides by the Rh(III)-Catalyzed Amidation of Aryl and Vinyl CH Bonds with Isocyanates Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 570–572 · CV · published

570124. Hesp, K. D.; Bergman, R. G.; Ellman, J. A. “Expedient Synthesis of N-Acyl Anthranilamides and571β-Enamine Amides by the Rh(III)-Catalyzed Amidation of Aryl and Vinyl CH Bonds with572Isocyanates” J. Am. Chem. Soc. 133, 11430–11433 (2011).

Institution fields

Peer reviewed
yes
First author
Hesp
Co-authors
Hesp, K. D.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Expedient Synthesis of N-Acyl Anthranilamides and β-Enamine Amides by the Rh(III)-Catalyzed Amidation of Aryl and Vinyl CH Bonds with IsocyanatesExpedient Synthesis of N-Acyl Anthranilamides and β-Enamine Amides by the Rh(III)-Catalyzed Amidation of Aryl and Vinyl C–H Bonds with IsocyanatesExpedient synthesis of N-acyl anthranilamides and β-enamine amides by the Rh (III)-catalyzed amidation of aryl and vinyl C–H bonds with isocyanates
year cv 201120112011
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja203495c10.1021/ja203495c
first author openalex HespHespHesp

Citations

OpenAlex
309
Scholar
305
DOI
10.1021/ja203495c
OpenAlex
W2040056655

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja203495c for expedient synthesis of N-acyl anthranilamides.
  • doi merged · 1.00 · Run 18
2011 Highly Functional Group Compatible Rh-Catalyzed Addition of Arylboroxines to Activated N-tert-Butanesulfinyl Ketimines Organic Letters article journal CV OA GS needs review

CV span

lines 574–576 · CV · published

574125. Joon, H. H.; Buesking, A. W.; Ellman, J. A. “Highly Functional Group Compatible Rh-Catalyzed575Addition of Arylboroxines to Activated N-tert-Butanesulfinyl Ketimines” Org. Lett. 13, 964-967576(2011).

Institution fields

Peer reviewed
yes
First author
Joon
Co-authors
Joon, H. H.; Buesking, A. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Functional Group Compatible Rh-Catalyzed Addition of Arylboroxines to Activated N-tert-Butanesulfinyl KetiminesHighly Functional Group Compatible Rh-Catalyzed Addition of Arylboroxines to Activated N-tert-Butanesulfinyl KetiminesHighly Functional Group Compatible Rh-Catalyzed Addition of Arylboroxines to Activated N-tert-Butanesulfinyl Ketimines
year cv 201120112011
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol201438k10.1021/ol201438k
first author openalex JoonJungJung

Citations

OpenAlex
87
Scholar
90
DOI
10.1021/ol201438k
OpenAlex
W2108659552

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol201438k for rh-catalyzed addition of arylboroxines.
  • doi merged · 1.00 · Run 18
2011 Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via CH Activation Organic Letters article journal CV OA GS needs review

CV span

lines 596–598 · CV · published

596131. Tsai, A. S.; Brasse, M.; Bergman, R. G.; Ellman, J. A. “Rh(III)-Catalyzed Oxidative Coupling of597Unactivated Alkenes via CH Activation” Org. Lett. 13, 540-542 (2011) [highlighted in Synfacts5982011, 4, 423].

Institution fields

Peer reviewed
yes
First author
Tsai
Co-authors
Tsai, A. S.; Brasse, M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via CH ActivationRh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H ActivationRh (III)-catalyzed oxidative coupling of unactivated alkenes via C− H activation
year cv 201120102011
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol102890k10.1021/ol102890k
first author openalex TsaiTsaiTsai

Citations

OpenAlex
281
Scholar
302
DOI
10.1021/ol102890k
OpenAlex
W2060022664

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol102890k for rh(iii)-catalyzed oxidative coupling.
  • doi merged · 1.00 · Run 18
2011 Rhodium(III)-Catalyzed Arylation of Boc-Imines via C-H Bond Functionalization Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 593–594 · CV · published

593130. Tsai, A. S.; Tauchert, M. E.; Bergman, R. G.; Ellman, J. A. “Rhodium(III)-Catalyzed Arylation of594Boc-Imines via C-H Bond Functionalization” J. Am. Chem. Soc. 133, 1248–1250 (2011).

Institution fields

Peer reviewed
yes
First author
Tsai
Co-authors
Tsai, A. S.; Tauchert, M. E.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium(III)-Catalyzed Arylation of Boc-Imines via C-H Bond FunctionalizationRhodium(III)-Catalyzed Arylation of Boc-Imines via C−H Bond FunctionalizationRhodium (III)-catalyzed arylation of boc-imines via C− H bond functionalization
year cv 201120112011
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja109562x10.1021/ja109562x
first author openalex TsaiTsaiTsai

Citations

OpenAlex
305
Scholar
316
DOI
10.1021/ja109562x
OpenAlex
W2088750596

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.201207995 for rhodium(iii)-catalyzed alkenyl C-H bond functionalization.
  • doi merged · 1.00 · Run 18
2011 Synthesis and Coordination Chemistry of Tri-Substituted Benzamidrazones Dalton Trans. article journal CV OA GS

CV span

lines 605–606 · CV · published

605133. Crimmin, M. R.; Colby, D. A.; Ellman, J. A.; Bergman, R. G. “Synthesis and Coordination606Chemistry of Tri-Substituted Benzamidrazones” J. Chem. Soc., Dalton Trans. 40, 514-522 (2011).

Institution fields

Peer reviewed
yes
First author
Crimmin
Co-authors
Crimmin, M. R.; Colby, D. A.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Coordination Chemistry of Tri-Substituted BenzamidrazonesSynthesis and coordination chemistry of tri-substituted benzamidrazones
year cv 20112010
venue crossref J. Chem. Soc., Dalton Trans.Dalton TransactionsDalton Trans.
kind cv articlearticle
DOI crossref 10.1039/c0dt01267j10.1039/c0dt01267j
first author openalex CrimminCrimmin

Citations

OpenAlex
7
Scholar
none
DOI
10.1039/c0dt01267j
OpenAlex
W2000480767

Match decisions

  • doi merged · 1.00 · Run 18
2011 Tubulysin D Analogues US Patent App article CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title scholar Tubulysin D Analogues
year scholar 2011
venue scholar US Patent App.
kind scholar other
first author scholar Ellman

Citations

OpenAlex
none
Scholar
30

Match decisions

No decision recorded; a single record.

2010 A Direct, Biomass-Based Synthesis of Benzoic Acid: Formic Acid-mediated Deoxygenation of the Glucose-Derived Materials Quinic Acid and Shikimic Acid ChemSusChem article journal CV OA GS

CV span

lines 637–639 · CV · published

637142. Arceo, E.; Ellman, J. A.; Bergman, R. G. “A Direct, Biomass-Based Synthesis of Benzoic Acid:638Formic Acid-mediated Deoxygenation of the Glucose-Derived Materials Quinic Acid and Shikimic639Acid” ChemSusChem 3, 811–813 (2010).

Institution fields

Peer reviewed
yes
First author
Arceo
Co-authors
Arceo, E.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv A Direct, Biomass-Based Synthesis of Benzoic Acid: Formic Acid-mediated Deoxygenation of the Glucose-Derived Materials Quinic Acid and Shikimic AcidA Direct, Biomass‐Based Synthesis of Benzoic Acid: Formic Acid‐Mediated Deoxygenation of the Glucose‐Derived Materials Quinic Acid and Shikimic AcidA direct, biomass-based synthesis of benzoic acid: formic acid-mediated deoxygenation of the glucose-derived materials quinic acid and shikimic acid
year cv 201020102011
venue crossref ChemSusChemChemSusChem
kind cv articlearticleother
DOI crossref 10.1002/cssc.20100011110.1002/cssc.201000111
first author openalex ArceoArceoArceo

Citations

OpenAlex
50
Scholar
63
DOI
10.1002/cssc.201000111
OpenAlex
W2120042511

Match decisions

  • doi merged · 1.00 · Run 18
2010 Aminopeptidase Fingerprints, an Integrated Approach for Identification of Good Substrates and Optimal Inhibitors Journal of Biological Chemistry article journal CV OA GS

CV span

lines 655–657 · CV · published

655147. Drag, M.; Bogyo, M.; Ellman, J. A.; Salvesen, G. S. “Aminopeptidase Fingerprints, an Integrated656Approach for Identification of Good Substrates and Optimal Inhibitors” J. Biol. Chem. 285, 3310-6573318 (2010).

Institution fields

Peer reviewed
yes
First author
Drag
Co-authors
Drag, M.; Bogyo, M.; Ellman, J. A.; Salvesen, G. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Aminopeptidase Fingerprints, an Integrated Approach for Identification of Good Substrates and Optimal InhibitorsAminopeptidase Fingerprints, an Integrated Approach for Identification of Good Substrates and Optimal InhibitorsAminopeptidase fingerprints, an integrated approach for identification of good substrates and optimal inhibitors
year cv 201020092010
venue crossref J. Biol. Chem.Journal of Biological ChemistryJournal of Biological ChemistryJournal of Biological Chemistry
kind cv articlearticleother
DOI crossref 10.1074/jbc.m109.06041810.1074/jbc.m109.060418
first author openalex DragDrągDrag

Citations

OpenAlex
103
Scholar
122
DOI
10.1074/jbc.m109.060418
OpenAlex
W2134606611

Match decisions

  • doi merged · 1.00 · Run 18
2010 Asymmetric Rh(I)-Catalyzed Addition of MIDA Boronates to N-tert-Butanesulfinyl Aldimines: Development and Comparison to Trifluoroborates The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 644–646 · CV · published

644144. Brak, K.; Ellman, J. A. “Asymmetric Rh(I)-Catalyzed Addition of MIDA Boronates to N-tert-645Butanesulfinyl Aldimines: Development and Comparison to Trifluoroborates” J. Org. Chem. 75,6463147–3150 (2010).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Rh(I)-Catalyzed Addition of MIDA Boronates to N-tert-Butanesulfinyl Aldimines: Development and Comparison to TrifluoroboratesAsymmetric Rh(I)-Catalyzed Addition of MIDA Boronates to N-tert-Butanesulfinyl Aldimines: Development and Comparison to TrifluoroboratesAsymmetric Rh(I)-Catalyzed Addition of MIDA Boronates to N-tert-Butanesulfinyl Aldimines: Development and Comparison to Trifluoroborates
year cv 201020102010
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo100318s10.1021/jo100318s
first author openalex BrakBrakBrak

Citations

OpenAlex
69
Scholar
75
DOI
10.1021/jo100318s
OpenAlex
W1975951968

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo100318s for MIDA boronates addition.
  • doi merged · 1.00 · Run 18
2010 Catalytic C-O Bond Cleavage of 2-Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin Related Polymers Journal of the American Chemical Society article journal CV OA GS

CV span

lines 611–613 · CV · published

611135. Nichols, J. M.; Bishop, L. M.; Bergman, R. G.; Ellman, J. A. “Catalytic C-O Bond Cleavage of 2-612Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin Related Polymers” J.613Am. Chem. Soc. 132, 12554-12555 (2010).

Institution fields

Peer reviewed
yes
First author
Nichols
Co-authors
Nichols, J. M.; Bishop, L. M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic C-O Bond Cleavage of 2-Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin Related PolymersCatalytic C−O Bond Cleavage of 2-Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin-Related PolymersCatalytic C−O Bond Cleavage of 2-Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin-Related PolymersCatalytic CO Bond Cleavage of 2-Aryloxy-1-Arylethanols and Its Application to the Depolymerization of Lignin Related Polymers
year cv 2010201020102010
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja106101f10.1021/ja106101f10.1021/ja109016b
first author openalex NicholsNicholsNicholsNichols

Also recorded as

  • W4214832928 (DOI 10.1021/ja109016b) · same title · 2010 Catalytic C−O Bond Cleavage of 2-Aryloxy-1-arylethanols and Its Application to the Depolymerization of Lignin-Related Polymers

Citations

OpenAlex
415
Scholar
490
DOI
10.1021/ja106101f
OpenAlex
W2005960625

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2010 ChemInform Abstract: Racemization Free Protocol for the Synthesis of N‐tert‐Butanesulfinyl Ketimines. ChemInform article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex ChemInform Abstract: Racemization Free Protocol for the Synthesis of N‐tert‐Butanesulfinyl Ketimines.Racemization Free Protocol for the Synthesis of N-tert-Butanesulfinyl Ketimines
year openalex 20102010
venue openalex ChemInformThe Journal of Organic Chemistry
kind openalex articleother
DOI openalex 10.1002/chin.201102065
first author openalex DattaDatta

Citations

OpenAlex
0
Scholar
38
DOI
10.1002/chin.201102065
OpenAlex
W2950034045

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo1011625 for racemization free protocol for ketimines.
  • fingerprint merged · 1.00 · Run 18
2010 Design and Synthesis of Novel Inhibitors for the Mycobacterium tuberculosis Phosphatase PtpB Organic & Biomolecular Chemistry article journal CV OA GS

CV span

lines 623–624 · CV · published

623138. Rawls, K. A.; Grundner, C.; Ellman, J. A. “Design and Synthesis of Novel Inhibitors for the624Mycobacterium tuberculosis Phosphatase PtpB” Org. Biomol. Chem. 8, 4066-4070 (2010).

Institution fields

Peer reviewed
yes
First author
Rawls
Co-authors
Rawls, K. A.; Grundner, C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design and Synthesis of Novel Inhibitors for the Mycobacterium tuberculosis Phosphatase PtpBDesign and synthesis of nonpeptidic, small molecule inhibitors for the Mycobacterium tuberculosis protein tyrosine phosphatase PtpBDesign and synthesis of nonpeptidic, small molecule inhibitors for the Mycobacterium tuberculosis protein tyrosine phosphatase PtpB
year cv 201020102010
venue crossref Org. Biomol. Chem.Organic & Biomolecular ChemistryOrganic & biomolecular chemistryOrganic & Biomolecular Chemistry
kind cv articlearticleother
DOI crossref 10.1039/c0ob00182a10.1039/c0ob00182a
first author openalex RawlsRawlsRawls

Citations

OpenAlex
26
Scholar
35
DOI
10.1039/c0ob00182a
OpenAlex
W2018273835

Match decisions

  • doi merged · 1.00 · Run 18
2010 Functional studies of the Plasmodium falciparum dipeptidyl aminopeptidase I (DPAP1) using small molecule inhibitors and active site Chemistry & Biology article journal CV OA GS

CV span

lines 626–628 · CV · published

626139. Deu, E.; Leyva, M.; Albrow, V.; Rice, M. J.; Ellman, J. A.; Bogyo, M. “Functional studies of the627Plasmodium falciparum dipeptidyl aminopeptidase I (DPAP1) using small molecule inhibitors and628active site” Chem. Biol. 17, 808-819 (2010).

Institution fields

Peer reviewed
yes
First author
Deu
Co-authors
Deu, E.; Leyva, M.; Albrow, V.; Rice, M. J.; Ellman, J. A.; Bogyo, M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Functional studies of the Plasmodium falciparum dipeptidyl aminopeptidase I (DPAP1) using small molecule inhibitors and active siteFunctional Studies of Plasmodium falciparum Dipeptidyl Aminopeptidase I Using Small Molecule Inhibitors and Active Site ProbesFunctional studies of Plasmodium falciparum dipeptidyl aminopeptidase I using small molecule inhibitors and active site probes
year cv 201020102010
venue crossref Chem. Biol.Chemistry & BiologyChemistry & biologyChemistry & Biology
kind cv articlearticleother
DOI crossref 10.1016/j.chembiol.2010.06.00710.1016/j.chembiol.2010.06.007
first author openalex DeuDeuDeu

Citations

OpenAlex
70
Scholar
82
DOI
10.1016/j.chembiol.2010.06.007
OpenAlex
W1984794626

Match decisions

  • doi merged · 1.00 · Run 18
2010 Identification and Evaluation of Novel Small Molecule Pan-Caspase Inhibitors in Huntington’s Disease Models Chemistry & Biology article journal CV OA GS

CV span

lines 618–621 · CV · published

618137. Leyva, M. J.; DeGiacomo, F.; Kaltenbach, L. S.; Holcomb, J.; Zhang, N.; Gafni, J.; Park, H.; Lo, D.619C.; Salvesen, G. S. Ellerby, L. M.; Ellman, J. A. “Identification and Evaluation of Novel Small620Molecule Pan-Caspase Inhibitors in Huntington’s Disease Models” Chem. Biol. 17, 1189-1200621(2010).

Institution fields

Peer reviewed
yes
First author
Leyva
Co-authors
Leyva, M. J.; DeGiacomo, F.; Kaltenbach, L. S.; Holcomb, J.; Zhang, N.; Gafni, J.; Park, H.; Lo, D. C.; Salvesen, G. S. Ellerby, L. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification and Evaluation of Novel Small Molecule Pan-Caspase Inhibitors in Huntington’s Disease ModelsIdentification and Evaluation of Small Molecule Pan-Caspase Inhibitors in Huntington's Disease ModelsIdentification and evaluation of small molecule pan-caspase inhibitors in Huntington's disease models
year cv 201020102010
venue crossref Chem. Biol.Chemistry & BiologyChemistry & biologyChemistry & Biology
kind cv articlearticleother
DOI crossref 10.1016/j.chembiol.2010.08.01410.1016/j.chembiol.2010.08.014
first author openalex LeyvaLeyvaLeyva

Citations

OpenAlex
54
Scholar
71
DOI
10.1016/j.chembiol.2010.08.014
OpenAlex
W2084399139

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1016/j.chembiol.2010.08.014 for pan-caspase inhibitors.
2010 Nonpeptidic Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors as Promising New Leads for Chagas Disease Chemotherapy Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 650–653 · CV · published

650146. Brak, K.; Kerr, I. D.; Barrett, K. T.; Fuchi, N.; Debnath, M.; Ang, K.; Engel, J. C.; McKerrow, J.651H.; Doyle, P. S.; Brinen, L. S.; Ellman, J. A. “Nonpeptidic Tetrafluorophenoxymethyl Ketone652Cruzain Inhibitors as Promising New Leads for Chagas Disease Chemotherapy” J. Med. Chem. 53,6531763–1773 (2010).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Kerr, I. D.; Barrett, K. T.; Fuchi, N.; Debnath, M.; Ang, K.; Engel, J. C.; McKerrow, J. H.; Doyle, P. S.; Brinen, L. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Nonpeptidic Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors as Promising New Leads for Chagas Disease ChemotherapyNonpeptidic Tetrafluorophenoxymethyl Ketone Cruzain Inhibitors as Promising New Leads for Chagas Disease ChemotherapyNonpeptidic tetrafluorophenoxymethyl ketone cruzain inhibitors as promising new leads for Chagas disease chemotherapy
year cv 201020102010
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm901633v10.1021/jm901633v
first author openalex BrakBrakBrak

Citations

OpenAlex
135
Scholar
174
DOI
10.1021/jm901633v
OpenAlex
W2120644129

Match decisions

  • doi merged · 1.00 · Run 18
2010 Preparation of 1,2,3-triazole substituted aryloxy methyl ketones as caspase inhibitors PCT Int. Appl. other CV OA GS

CV span

lines 1474–1475 · CV · published

14746. Ellerby, L. M.; Ellman, J. A.; Leyva, M. J. “Preparation of 1,2,3-triazole substituted aryloxy methyl1475ketones as caspase inhibitors” PCT Int. Appl. (2010), WO 2010017408 A1 20100211.

Institution fields

Peer reviewed
none
First author
Ellerby
Co-authors
Ellerby, L. M.; Ellman, J. A.; Leyva, M. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of 1,2,3-triazole substituted aryloxy methyl ketones as caspase inhibitors
year cv 2010
venue cv PCT Int. Appl.
kind cv other
first author cv Ellerby

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2010 Racemization Free Protocol for the Synthesis “N-tert-Butanesulfinyl Ketimimes The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 615–616 · CV · published

615136. Datta, G. K.; Ellman, J. A. “Racemization Free Protocol for the Synthesis “N-tert-Butanesulfinyl616Ketimimes” J. Org. Chem. 75, 6283-6285 (2010).

Institution fields

Peer reviewed
yes
First author
Datta
Co-authors
Datta, G. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Racemization Free Protocol for the Synthesis “N-tert-Butanesulfinyl KetimimesRacemization Free Protocol for the Synthesis ofN-tert-Butanesulfinyl Ketimines
year cv 20102010
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/jo101162510.1021/jo1011625
first author openalex DattaDatta

Citations

OpenAlex
29
Scholar
none
DOI
10.1021/jo1011625
OpenAlex
W1987707452

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo1011625 for racemization free protocol for ketimines.
  • doi merged · 1.00 · Run 18
2010 Rhenium-Catalyzed Didehydroxylation of Vicinal Diols to Alkenes Using a Simple Alcohol as a Reducing Agent Journal of the American Chemical Society article journal CV OA GS

CV span

lines 630–632 · CV · published

630140. Arceo, E.; Ellman, J. A.; Bergman, R. G. “Rhenium-Catalyzed Didehydroxylation of Vicinal Diols631to Alkenes Using a Simple Alcohol as a Reducing Agent” J. Am. Chem. Soc. 132, 11408–11409632(2010).

Institution fields

Peer reviewed
yes
First author
Arceo
Co-authors
Arceo, E.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhenium-Catalyzed Didehydroxylation of Vicinal Diols to Alkenes Using a Simple Alcohol as a Reducing AgentRhenium-Catalyzed Didehydroxylation of Vicinal Diols to Alkenes Using a Simple Alcohol as a Reducing AgentRhenium-catalyzed didehydroxylation of vicinal diols to alkenes using a simple alcohol as a reducing agent
year cv 201020102010
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja103436v10.1021/ja103436v
first author openalex ArceoArceoArceo

Citations

OpenAlex
171
Scholar
190
DOI
10.1021/ja103436v
OpenAlex
W2115355513

Match decisions

  • doi merged · 1.00 · Run 18
2010 Rh(I)-Catalyzed Direct Arylation of Azines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 608–609 · CV · published

608134. Berman, A. M.; Bergman, R. G.; Ellman, J. A. “Rh(I)-Catalyzed Direct Arylation of Azines” J.609Org. Chem. 75, 7863–7868 (2010).

Institution fields

Peer reviewed
yes
First author
Berman
Co-authors
Berman, A. M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(I)-Catalyzed Direct Arylation of AzinesRh(I)-Catalyzed Direct Arylation of AzinesRh (I)-catalyzed direct arylation of azines
year cv 201020102010
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo101793r10.1021/jo101793r
first author openalex BermanBermanBerman

Citations

OpenAlex
101
Scholar
102
DOI
10.1021/jo101793r
OpenAlex
W2061147177

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/ja8059396 for rh(i)-catalyzed direct arylation of pyridines and quinolines.
2010 Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation Chemical Reviews article journal CV OA GS

CV span

lines 663–664 · CV · published

663149. Colby, D. A.; Bergman, R. G.; Ellman, J. A. “Rhodium-Catalyzed C-C Bond Formation via664Heteroatom-Directed C-H Bond Activation” Chem. Rev. 110, 624-655 (2010).

Institution fields

Peer reviewed
yes
First author
Colby
Co-authors
Colby, D. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond ActivationRhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond ActivationRhodium-catalyzed CC bond formation via heteroatom-directed CH bond activation
year cv 201020092010
venue crossref Chem. Rev.Chemical ReviewsChemical ReviewsChemical Reviews
kind cv articlereviewother
DOI crossref 10.1021/cr900005n10.1021/cr900005n
first author openalex ColbyColbyColby

Citations

OpenAlex
3691
Scholar
3913
DOI
10.1021/cr900005n
OpenAlex
W2050791488

Match decisions

  • doi merged · 1.00 · Run 18
2010 Synthesis and Applications of tert-Butanesulfinamide Chemical Reviews article journal CV OA GS needs review

CV span

lines 641–642 · CV · published

641143. Robak, M. T.; Herbage, M. A.; Ellman, J. A. “Synthesis and Applications of tert-642Butanesulfinamide” Chem. Rev. 110, 3600–3740 (2010).

Institution fields

Peer reviewed
yes
First author
Robak
Co-authors
Robak, M. T.; Herbage, M. A.; Ellman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Applications of tert-ButanesulfinamideSynthesis and Applications of tert-ButanesulfinamideSynthesis and Applications of tert-Butanesulfinamide
year cv 201020102010
venue crossref Chem. Rev.Chemical ReviewsChemical reviewsChemical Reviews
kind cv articlereviewother
DOI crossref 10.1021/cr900382t10.1021/cr900382t
first author openalex RobakRobakRobak

Citations

OpenAlex
1159
Scholar
1353
DOI
10.1021/cr900382t
OpenAlex
W2075813623

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/cr900382t for synthesis and applications of tert-butanesulfinamide review.
  • doi merged · 1.00 · Run 18
2010 Synthesis of Multicyclic Pyridine and Quinoline Derivatives via Intramolecular C-H Bond Functionalization Organic Letters article journal CV OA GS

CV span

lines 634–635 · CV · published

634141. Yotphan, S.; Bergman, R. G.; Ellman, J. A. “Synthesis of Multicyclic Pyridine and Quinoline635Derivatives via Intramolecular C-H Bond Functionalization” Org. Lett. 12, 2978-2981 (2010).

Institution fields

Peer reviewed
yes
First author
Yotphan
Co-authors
Yotphan, S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Multicyclic Pyridine and Quinoline Derivatives via Intramolecular C-H Bond FunctionalizationSynthesis of Multicyclic Pyridine and Quinoline Derivatives via Intramolecular C−H Bond FunctionalizationSynthesis of multicyclic pyridine and quinoline derivatives via intramolecular CH bond functionalization
year cv 201020102010
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol101002b10.1021/ol101002b
first author openalex YotphanYotphanYotphan

Citations

OpenAlex
58
Scholar
59
DOI
10.1021/ol101002b
OpenAlex
W2085032660

Match decisions

  • doi merged · 1.00 · Run 18
2010 Time-Resolved Single-Step Protease Activity Quantification Using Nanoplasmonic Resonator Sensors ACS Nano article journal CV OA GS

CV span

lines 659–661 · CV · published

659148. Sun, C.; Su, K.-H.; Valentine, J.; Rosa-Bauza, Y. T.; Ellman, J. A.; Elboudwarej, O.; Mukherjee,660B.; Craik, C. S.; Shuman, M. A.; Chen, F. F.; Zhang, X. “Time-Resolved Single-Step Protease661Activity Quantification Using Nanoplasmonic Resonator Sensors” ACS Nano 4, 978–984 (2010).

Institution fields

Peer reviewed
yes
First author
Sun
Co-authors
Sun, C.; Su, K.-H.; Valentine, J.; Rosa-Bauza, Y. T.; Ellman, J. A.; Elboudwarej, O.; Mukherjee, B.; Craik, C. S.; Shuman, M. A.; Chen, F. F.; Zhang, X.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Time-Resolved Single-Step Protease Activity Quantification Using Nanoplasmonic Resonator SensorsTime-Resolved Single-Step Protease Activity Quantification Using Nanoplasmonic Resonator SensorsTime resolved single-step protease activity quantification using nanoplasmonic resonator sensors
year cv 201020102010
venue crossref ACS NanoACS NanoACS nano
kind cv articlearticleother
DOI crossref 10.1021/nn900757p10.1021/nn900757p
first author openalex SunSunSun

Citations

OpenAlex
38
Scholar
49
DOI
10.1021/nn900757p
OpenAlex
W4242896475

Match decisions

  • doi merged · 1.00 · Run 18
2010 Total Synthesis of (-)-Aurantioclavine Organic Letters article journal CV OA GS needs review

CV span

lines 648–648 · CV · published

648145. Brak, K.; Ellman, J. A. “Total Synthesis of (-)-Aurantioclavine” Org. Lett. 12, 2004–2007 (2010).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Total Synthesis of (-)-AurantioclavineTotal Synthesis of (−)-AurantioclavineTotal Synthesis of (−)-AurantioclavineTotal synthesis of (−)-aurantioclavine
year cv 2010201020102010
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic lettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol100470g10.1021/ol100470g10.1021/ol100909b
first author openalex BrakBrakBrakBrak

Also recorded as

Citations

OpenAlex
86
Scholar
99
DOI
10.1021/ol100470g
OpenAlex
W1975252703

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol100470g for total synthesis of (-)-aurantioclavine.
  • doi merged · 1.00 · Run 18
2009 An Efficient Didehydroxylation Method for the Biomass-Derived Polyols Glycerol and Erythritol. Mechanistic Studies of a Formic Acid-Mediated Deoxygenation Chemical Communications article journal CV OA GS

CV span

lines 677–679 · CV · published

677153. Arceo, E.; Marsden, P.; Bergman, R. G.; Ellman, J. A. “An Efficient Didehydroxylation Method for678the Biomass-Derived Polyols Glycerol and Erythritol. Mechanistic Studies of a Formic Acid-679Mediated Deoxygenation” Chem. Commun. 3357-3359 (2009).

Institution fields

Peer reviewed
yes
First author
Arceo
Co-authors
Arceo, E.; Marsden, P.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv An Efficient Didehydroxylation Method for the Biomass-Derived Polyols Glycerol and Erythritol. Mechanistic Studies of a Formic Acid-Mediated DeoxygenationAn efficient didehydroxylation method for the biomass-derived polyols glycerol and erythritol. Mechanistic studies of a formic acid-mediated deoxygenationAn efficient didehydroxylation method for the biomass-derived polyols glycerol and erythritol. Mechanistic studies of a formic acid-mediated deoxygenation
year cv 200920092009
venue crossref Chem. Commun.Chemical CommunicationsChemical communicationsChemical Communications
kind cv articlearticleother
DOI crossref 10.1039/b907746d10.1039/b907746d
first author openalex ArceoArceoArceo

Citations

OpenAlex
126
Scholar
117
DOI
10.1039/b907746d
OpenAlex
W2054936443

Match decisions

  • doi merged · 1.00 · Run 18
2009 Application of Daugulis Copper-Catalyzed Direct Arylation to the Synthesis of 5-Aryl Benzotriazepines Organic Letters article journal CV OA GS needs review

CV span

lines 693–694 · CV · published

693157. Yotphan, S.; Bergman, R. G.; Ellman, J. A. “Application of Daugulis Copper-Catalyzed Direct694Arylation to the Synthesis of 5-Aryl Benzotriazepines” Org. Lett. 11, 1511–1514 (2009).

Institution fields

Peer reviewed
yes
First author
Yotphan
Co-authors
Yotphan, S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Application of Daugulis Copper-Catalyzed Direct Arylation to the Synthesis of 5-Aryl BenzotriazepinesApplication of Daugulis Copper-Catalyzed Direct Arylation to the Synthesis of 5-Aryl BenzotriazepinesApplication of Daugulis copper-catalyzed direct arylation to the synthesis of 5-aryl benzotriazepines
year cv 200920092009
venue crossref Org. Lett.Organic LettersOrganic lettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol900103a10.1021/ol900103a
first author openalex YotphanYotphanYotphan

Citations

OpenAlex
83
Scholar
96
DOI
10.1021/ol900103a
OpenAlex
W2033491930

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ol900103a for application of daugulis copper-catalyzed direct arylation.
  • doi merged · 1.00 · Run 18
2009 Asymmetric Synthesis of α–Branched Allylic Amines by the Rh(I)-Catalyzed Addition of Alkenyltrifluoroborates to N-tert-Butanesulfinyl Aldimines Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 689–691 · CV · published

689156. Brak, K.; Ellman, J. A. “Asymmetric Synthesis of α–Branched Allylic Amines by the Rh(I)-690Catalyzed Addition of Alkenyltrifluoroborates to N-tert-Butanesulfinyl Aldimines” J. Am. Chem.691Soc. 131, 3850–3851 (2009).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of α–Branched Allylic Amines by the Rh(I)-Catalyzed Addition of Alkenyltrifluoroborates to N-tert-Butanesulfinyl AldiminesAsymmetric Synthesis of α-Branched Allylic Amines by the Rh(I)-Catalyzed Addition of Alkenyltrifluoroborates to N - tert -Butanesulfinyl AldiminesAsymmetric Synthesis of α-Branched Allylic Amines by the Rh(I)-Catalyzed Addition of Alkenyltrifluoroborates to N-tert-Butanesulfinyl Aldimines
year cv 200920092009
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja900260310.1021/ja9002603
first author openalex BrakBrakBrak

Citations

OpenAlex
97
Scholar
110
DOI
10.1021/ja9002603
OpenAlex
W2014689586

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja9002603 for asymmetric synthesis of alpha-branched allylic amines.
  • doi merged · 1.00 · Run 18
2009 Enantioselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea Organocatalysis Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 674–675 · CV · published

674152. Kimmel, K. L.; Robak, M. T.; Ellman, J. A. “Enantioselective Addition of Thioacetic Acid to675Nitroalkenes via N-Sulfinyl Urea Organocatalysis” J. Am. Chem. Soc. 131, 8754–8755 (2009).

Institution fields

Peer reviewed
yes
First author
Kimmel
Co-authors
Kimmel, K. L.; Robak, M. T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea OrganocatalysisEnantioselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea OrganocatalysisEnantioselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea Organocatalysis
year cv 200920092009
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja903351a10.1021/ja903351a
first author openalex KimmelKimmelKimmel

Citations

OpenAlex
169
Scholar
188
DOI
10.1021/ja903351a
OpenAlex
W2047776476

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja903351a for enantioselective addition of thioacetic acid.
  • doi merged · 1.00 · Run 18
2009 Fluorogenic Materials and Uses Thereof U.S. Patent No. 7,629,437 other CV OA GS

CV span

lines 1421–1422 · CV · published

14219. Harris, J. L.; Backes, B. J.; Ellman, J. A.; Craig, C. S. “Fluorogenic Materials and Uses Thereof”1422U.S. (2009), Patent No. 7,629,437.

Institution fields

Peer reviewed
none
First author
Harris
Co-authors
Harris, J. L.; Backes, B. J.; Ellman, J. A.; Craig, C. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Fluorogenic Materials and Uses Thereof
year cv 2009
venue cv U.S. Patent No. 7,629,437
kind cv other
first author cv Harris

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2009 Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA Bioorganic & Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 666–668 · CV · published

666150. Rawls, K. A.; Lang, T. P.; Takeuchi, J.; Imamura, S.; Baguley, T. D.; Grundner, C.; Alber, T.;667Ellman, J. A. “Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis668protein tyrosine phosphatase PtpA” Bioorg. Med. Chem. Lett. 19, 6851-6854 (2009).

Institution fields

Peer reviewed
yes
First author
Rawls
Co-authors
Rawls, K. A.; Lang, T. P.; Takeuchi, J.; Imamura, S.; Baguley, T. D.; Grundner, C.; Alber, T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpAFragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpAFragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA
year cv 200920092009
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic & Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/j.bmcl.2009.10.09010.1016/j.bmcl.2009.10.090
first author openalex RawlsRawlsRawls

Citations

OpenAlex
52
Scholar
67
DOI
10.1016/j.bmcl.2009.10.090
OpenAlex
W2058922600

Match decisions

  • doi merged · 1.00 · Run 18
2009 General One-pot Method for the Preparation of N-tert-Butanesulfinyl Amine Diastereomer Mixtures as Standards for Stereoselectivity Determinations The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 685–687 · CV · published

685155. Brak, K.; Barrett, K. T.; Ellman, J. A. “General One-pot Method for the Preparation of N-tert-686Butanesulfinyl Amine Diastereomer Mixtures as Standards for Stereoselectivity Determinations” J.687Org. Chem. 74, 3606-3608 (2009).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Barrett, K. T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General One-pot Method for the Preparation of N-tert-Butanesulfinyl Amine Diastereomer Mixtures as Standards for Stereoselectivity DeterminationsGeneral One-Pot Method for the Preparation of N-tert-Butanesulfinylamine Diastereomer Mixtures as Standards for Stereoselectivity Determinations
year cv 20092009
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticle
DOI crossref 10.1021/jo900353p10.1021/jo900353p
first author openalex BrakBrak

Citations

OpenAlex
17
Scholar
none
DOI
10.1021/jo900353p
OpenAlex
W2043958672

Match decisions

  • doi merged · 1.00 · Run 18
2009 Method of converting a polyol to olefin U.S. Pat. Appl. Publ. version 2012 Method of Converting a Polyol to an Olefin other CV OA GS

CV span

lines 1477–1478 · CV · published

14777. Bergman, R. G.; Ellman, J. A.; Arceo Rebollo, E.; Marsden, P. C. “Method of converting a polyol1478to olefin” U.S. Pat. Appl. Publ. (2009), US 20090287004 A1 20091119.

Institution fields

Peer reviewed
none
First author
Bergman
Co-authors
Bergman, R. G.; Ellman, J. A.; Arceo Rebollo, E.; Marsden, P. C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Method of converting a polyol to olefin
year cv 2009
venue cv U.S. Pat. Appl. Publ.
kind cv other
first author cv Bergman

Citations

OpenAlex
none
Scholar
none
Scholar with related records
28

Match decisions

No decision recorded; a single record.

2009 Preparation of tubulysin D analogs as highly potent cell-growth inhibitors for treating cancer and psoriasis PCT Int. Appl. other CV OA GS

CV span

lines 1492–1494 · CV · published

149211. Ellman, J. A.; Patterson, A. W.; Peltier, H. “Preparation of tubulysin D analogs as highly potent1493cell-growth inhibitors for treating cancer and psoriasis” PCT Int. Appl. (2009), WO 20090129581494A2 20090129.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J. A.; Patterson, A. W.; Peltier, H.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of tubulysin D analogs as highly potent cell-growth inhibitors for treating cancer and psoriasis
year cv 2009
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2009 Real-time, single-step bioassay using nanoplasmonic resonator comprising metallic nanodisks and having a tagged biomol PCT Int. Appl. other CV OA GS

CV span

lines 1480–1483 · CV · published

14808. Chen, F. F.; Ellman, J. A.; Zhang, X. “Real-time, single-step bioassay using nanoplasmonic1481resonator comprising metallic nanodisks and having a tagged biomol” PCT Int. Appl. (2009), WO14822009094058 A2 20090730.1483

Institution fields

Peer reviewed
none
First author
Chen
Co-authors
Chen, F. F.; Ellman, J. A.; Zhang, X.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Real-time, single-step bioassay using nanoplasmonic resonator comprising metallic nanodisks and having a tagged biomol
year cv 2009
venue cv PCT Int. Appl.
kind cv other
first author cv Chen

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2009 Recycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-Butanesulfinamide The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 696–698 · CV · published

696158. Wakayama, M.; Ellman, J. A. “Recycling the tert-Butanesulfinyl Group in the Synthesis of Amines697Using tert-Butanesulfinamide” J. Org. Chem. 74, 2646–2650 (2009) [JOC Feature article and698highlighted by Trevor Laird and coauthors in Org. Proc. Res. Dev. 2009, 13, 364–370].

Institution fields

Peer reviewed
yes
First author
Wakayama
Co-authors
Wakayama, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Recycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-ButanesulfinamideRecycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-ButanesulfinamideRecycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-Butanesulfinamide
year cv 200920092009
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo900188310.1021/jo9001883
first author openalex WakayamaWakayamaWakayama

Citations

OpenAlex
78
Scholar
118
DOI
10.1021/jo9001883
OpenAlex
W2013639276

Match decisions

  • doi merged · 1.00 · Run 18
2009 Rhodium-Catalyzed Enantioselective Addition of Arylboronic Acids to In Situ Generated N-Boc Arylimines. Preparation of (S)-tert-Butyl (4-Chlorophenyl)(Thiophen-2-yl-MethyylCarbamate Organic Syntheses article journal CV OA GS

CV span

lines 670–672 · CV · published

670151. Storgaard, M.; Ellman, J. A. “Rhodium-Catalyzed Enantioselective Addition of Arylboronic Acids671to In Situ Generated N-Boc Arylimines. Preparation of (S)-tert-Butyl (4-Chlorophenyl)(Thiophen-2-672yl-MethyylCarbamate” Org. Synth. 86, 360-373 (2009).

Institution fields

Peer reviewed
yes
First author
Storgaard
Co-authors
Storgaard, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed Enantioselective Addition of Arylboronic Acids to In Situ Generated N-Boc Arylimines. Preparation of (S)-tert-Butyl (4-Chlorophenyl)(Thiophen-2-yl-MethyylCarbamateRhodium‐Catalyzed Enantioselective Addition of Arylboronic Acids to in situ Generated N ‐Boc Arylimines. Preparation of ( S )‐ tert ‐Butyl (4‐Chlorophenyl)(Thiophen‐2‐Yl)Methylcarbamate
year cv 20092009
venue crossref Org. Synth.Organic SynthesesOrganic Syntheses
kind cv articleother
DOI crossref 10.1002/0471264229.os086.3410.1002/0471264229.os086.34
first author openalex StorgaardStorgaard

Citations

OpenAlex
0
Scholar
none
DOI
10.1002/0471264229.os086.34
OpenAlex
W2100517367

Match decisions

  • doi merged · 1.00 · Run 18
2009 Rhodium Catalyzed Enantioselective Cylization of Substituted Imidazoles via C–H Bond Activation Chemical Communications article journal CV OA GS needs review

CV span

lines 681–683 · CV · published

681154. Tsai, A. S.; Wilson, R. M.; Hirada, H.; Bergman, R. G.; Ellman, J. A. “Rhodium Catalyzed682Enantioselective Cylization of Substituted Imidazoles via C–H Bond Activation” Chem. Commun.6833910-3912 (2009). Special issue: Catalysis in Organic Synthesis.

Institution fields

Peer reviewed
yes
First author
Tsai
Co-authors
Tsai, A. S.; Wilson, R. M.; Hirada, H.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium Catalyzed Enantioselective Cylization of Substituted Imidazoles via C–H Bond ActivationRhodium catalyzed enantioselective cyclization of substituted imidazoles via C–H bond activationRhodium catalyzed enantioselective cyclization of substituted imidazoles via C–H bond activation
year cv 200920092009
venue crossref Chem. Commun.Chemical CommunicationsChemical CommunicationsChemical Communications
kind cv articlearticleother
DOI crossref 10.1039/b902878a10.1039/b902878a
first author openalex TsaiTsaiTsai

Citations

OpenAlex
84
Scholar
49
DOI
10.1039/b902878a
OpenAlex
W2049186094

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1039/b902878a for rhodium catalyzed enantioselective cyclization.
  • doi merged · 1.00 · Run 18
2009 SERS-based, single step, real-time detection of protein kinase and/or phosphatase activity utilizing Raman active surface comprising nanoscale features PCT Int. Appl. other CV OA GS

CV span

lines 1484–1486 · CV · published

14849. Chen, F. F.; Liu, G. L.; Ellman, J. A. “SERS-based, single step, real-time detection of protein1485kinase and/or phosphatase activity utilizing Raman active surface comprising nanoscale features”1486PCT Int. Appl. (2009), WO 2009088779 A2 20090716.

Institution fields

Peer reviewed
none
First author
Chen
Co-authors
Chen, F. F.; Liu, G. L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv SERS-based, single step, real-time detection of protein kinase and/or phosphatase activity utilizing Raman active surface comprising nanoscale features
year cv 2009
venue cv PCT Int. Appl.
kind cv other
first author cv Chen

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2009 Triazole derivatives and aminocoumarin derivatives as nonpeptidic inhibitors of cruzain and their preparation and use in the treatment of Chagas disease PCT Int. Appl. other CV OA GS

CV span

lines 1488–1490 · CV · published

148810. Ellman, J. A.; Brak, K. “Triazole derivatives and aminocoumarin derivatives as nonpeptidic1489inhibitors of cruzain and their preparation and use in the treatment of Chagas disease” PCT Int.1490Appl. (2009), WO 2009075778 A2 20090618.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J. A.; Brak, K.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Triazole derivatives and aminocoumarin derivatives as nonpeptidic inhibitors of cruzain and their preparation and use in the treatment of Chagas disease
year cv 2009
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2008 Asymmetric Copper-Catalyzed Synthesis of -Amino Boronate Esters from N-tert-Butanesulfinyl Aldimines Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 718–719 · CV · published

718164. Beenen, M. A.; An, C.; Ellman, J. A. “Asymmetric Copper-Catalyzed Synthesis of -Amino719Boronate Esters from N-tert-Butanesulfinyl Aldimines” J. Am. Chem. Soc. 130, 6910-6911 (2008).

Institution fields

Peer reviewed
yes
First author
Beenen
Co-authors
Beenen, M. A.; An, C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Copper-Catalyzed Synthesis of -Amino Boronate Esters from N-tert-Butanesulfinyl AldiminesAsymmetric Copper-Catalyzed Synthesis of α-Amino Boronate Esters from N - tert -Butanesulfinyl AldiminesAsymmetric Copper-Catalyzed Synthesis of α-Amino Boronate Esters from N-tert-Butanesulfinyl Aldimines
year cv 200820082008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja800829y10.1021/ja800829y
first author openalex BeenenBeenenBeenen

Citations

OpenAlex
229
Scholar
277
DOI
10.1021/ja800829y
OpenAlex
W2023115089

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja800829y for asymmetric copper-catalyzed synthesis of amino boronate esters.
  • doi merged · 1.00 · Run 18
2008 Asymmetric Synthesis of (−)-Incarvillateine Employing an Intramolecular Alkylation via Rh-Catalyzed Olefinic C−H Bond Activation Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 730–732 · CV · published

730168. Tsai, A. S.; Bergman, R. G.; Ellman, J. A. “Asymmetric Synthesis of (−)-Incarvillateine Employing731an Intramolecular Alkylation via Rh-Catalyzed Olefinic C−H Bond Activation” J. Am. Chem. Soc.732130, 6316-6317 (2008).

Institution fields

Peer reviewed
yes
First author
Tsai
Co-authors
Tsai, A. S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of (−)-Incarvillateine Employing an Intramolecular Alkylation via Rh-Catalyzed Olefinic C−H Bond ActivationAsymmetric Synthesis of (−)-Incarvillateine Employing an Intramolecular Alkylation via Rh-Catalyzed Olefinic C–H Bond Activation
year cv 20082008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articleother
DOI crossref 10.1021/ja8012159
first author cv TsaiTsai

Citations

OpenAlex
none
Scholar
122
DOI
10.1021/ja8012159

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja8012159 for asymmetric synthesis of (-)-incarvillateine.
  • fingerprint merged · 1.00 · Run 18
2008 Conversion of glycerol from biodiesel production to allyl alcohol PCT Int. Appl. other CV OA GS

CV span

lines 1496–1497 · CV · published

149612. Bergman, R. G.; Ellman, J. A.; Arceo Rebollo, E. “Conversion of glycerol from biodiesel1497production to allyl alcohol” PCT Int. Appl. (2008), WO 2008092115 A1 20080731.

Institution fields

Peer reviewed
none
First author
Bergman
Co-authors
Bergman, R. G.; Ellman, J. A.; Arceo Rebollo, E.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Conversion of glycerol from biodiesel production to allyl alcohol
year cv 2008
venue cv PCT Int. Appl.
kind cv other
first author cv Bergman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2008 Detection of protease using a single peptide-nanocrescent hybrid SERS probe, and diagnostic applications PCT Int. Appl. other CV OA GS

CV span

lines 1499–1501 · CV · published

149913. Liu, G. L.; Ellman, J. A.; Lee, L. P.; Chen, F. F. “Detection of protease using a single peptide-1500nanocrescent hybrid SERS probe, and diagnostic applications” PCT Int. Appl. (2008), WO15012008018933 A2 20080214.

Institution fields

Peer reviewed
none
First author
Liu
Co-authors
Liu, G. L.; Ellman, J. A.; Lee, L. P.; Chen, F. F.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Detection of protease using a single peptide-nanocrescent hybrid SERS probe, and diagnostic applications
year cv 2008
venue cv PCT Int. Appl.
kind cv other
first author cv Liu

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2008 Direct Functionalization of Nitrogen Heterocycles via Rh-Catalyzed CH Bond Activation Accounts of Chemical Research article journal CV OA GS needs review

CV span

lines 707–708 · CV · published

707161. Lewis, J. C.; Bergman, R. G.; Ellman, J. A. “Direct Functionalization of Nitrogen Heterocycles via708Rh-Catalyzed CH Bond Activation” Acc. Chem. Res. 41, 1013-1025 (2008).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Direct Functionalization of Nitrogen Heterocycles via Rh-Catalyzed CH Bond ActivationDirect Functionalization of Nitrogen Heterocycles via Rh-Catalyzed C−H Bond ActivationDirect functionalization of nitrogen heterocycles via Rh-catalyzed CH bond activation
year cv 200820082008
venue crossref Acc. Chem. Res.Accounts of Chemical ResearchAccounts of chemical researchAccounts of Chemical Research
kind cv articlearticleother
DOI crossref 10.1021/ar800042p10.1021/ar800042p
first author openalex LewisLewisLewis

Citations

OpenAlex
970
Scholar
1047
DOI
10.1021/ar800042p
OpenAlex
W2072243238

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ar800042p for direct functionalization of nitrogen heterocycles review.
  • doi merged · 1.00 · Run 18
2008 Enantioselective Intramolecular Hydroarylation of Alkenes via Directed C-H Bond Activation The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 703–705 · CV · published

703160. Harada, H.; Thalji, R. K.; Bergman, R. G.; Ellman, J. A. “Enantioselective Intramolecular704Hydroarylation of Alkenes via Directed C-H Bond Activation” J. Org. Chem. 73, 6772-6779705(2008).

Institution fields

Peer reviewed
yes
First author
Harada
Co-authors
Harada, H.; Thalji, R. K.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Intramolecular Hydroarylation of Alkenes via Directed C-H Bond ActivationEnantioselective intramolecular hydroarylation of alkenes via directed C− H bond activation
year cv 20082008
venue crossref J. Org. Chem.The Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articleother
DOI crossref 10.1021/jo801098z
first author cv HaradaHarada

Citations

OpenAlex
none
Scholar
165
DOI
10.1021/jo801098z

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo801098z for enantioselective intramolecular hydroarylation.
  • fingerprint merged · 1.00 · Run 18
2008 Enantioselective Synthesis of -Aryl Alkylamines by Rh-Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic Imines Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 714–716 · CV · published

714163. Trincado, M.; Ellman, J. A. “Enantioselective Synthesis of -Aryl Alkylamines by Rh-Catalyzed715Addition Reactions of Arylboronic Acids to Aliphatic Imines” Angew. Chem. Int. Ed. 47, 5623-7165626 (2008).

Institution fields

Peer reviewed
yes
First author
Trincado
Co-authors
Trincado, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Synthesis of -Aryl Alkylamines by Rh-Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic IminesEnantioselective Synthesis of α‐Aryl Alkylamines by Rh‐Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic IminesEnantioselective Synthesis of α‐Aryl Alkylamines by Rh‐Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic IminesEnantioselective Synthesis of α‐Aryl Alkylamines by Rh‐Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic Imines
year cv 2008200820082008
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticleother
DOI crossref 10.1002/anie.20080113710.1002/anie.20080113710.1002/ange.200801137
first author openalex TrincadoTrincadoTrincadoTrincado

Also recorded as

  • W4244231638 (DOI 10.1002/ange.200801137) · same title · 2008 Enantioselective Synthesis of α‐Aryl Alkylamines by Rh‐Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic Imines

Citations

OpenAlex
80
Scholar
82
DOI
10.1002/anie.200801137
OpenAlex
W2130790154

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.200801137 for enantioselective synthesis of alpha-aryl alkylamines.
  • doi merged · 1.00 · Run 18
2008 Expedient Synthesis of N-Methyl Tubulysin Analogues with High Cytotoxicity The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 721–722 · CV · published

721165. Patterson, A. W.; Peltier, H. M.; Ellman, J. A. “Expedient Synthesis of N-Methyl Tubulysin722Analogues with High Cytotoxicity” J. Org. Chem. 73, 4362-4369 (2008) [Featured Article].

Institution fields

Peer reviewed
yes
First author
Patterson
Co-authors
Patterson, A. W.; Peltier, H. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Expedient Synthesis of N-Methyl Tubulysin Analogues with High CytotoxicityExpedient Synthesis of N-Methyl Tubulysin Analogues with High CytotoxicityExpedient Synthesis of N-Methyl Tubulysin Analogues with High Cytotoxicity
year cv 200820082008
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo800384x10.1021/jo800384x
first author openalex PattersonPattersonPatterson

Citations

OpenAlex
59
Scholar
98
DOI
10.1021/jo800384x
OpenAlex
W2014634108

Match decisions

  • doi merged · 1.00 · Run 18
2008 Identification of a New Class of Nonpeptidic Inhibitors of Cruzain Journal of the American Chemical Society article journal CV OA GS

CV span

lines 727–728 · CV · published

727167. Brak, K.; Doyle, P. S.; McKerrow, J. H.; Ellman, J. A. “Identification of a New Class of728Nonpeptidic Inhibitors of Cruzain” J. Am. Chem. Soc. 130, 6404-6410 (2008).

Institution fields

Peer reviewed
yes
First author
Brak
Co-authors
Brak, K.; Doyle, P. S.; McKerrow, J. H.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of a New Class of Nonpeptidic Inhibitors of CruzainIdentification of a New Class of Nonpeptidic Inhibitors of CruzainIdentification of a new class of nonpeptidic inhibitors of cruzain
year cv 200820082008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja710254m10.1021/ja710254m
first author openalex BrakBrakBrak

Citations

OpenAlex
130
Scholar
180
DOI
10.1021/ja710254m
OpenAlex
W1964356444

Match decisions

  • doi merged · 1.00 · Run 18
2008 Positional-Scanning Fluorogenic Substrate Libraries Reveal Unexpected Specificity Determinants of Deubiquitinating Enzymes (DUBs) Biochemical Journal article journal CV OA GS

CV span

lines 710–712 · CV · published

710162. Drag, M.; Mikolajczyk, J.; Bekes, M.; Reyes-Turcu, F.; Ellman, J. A.; Wilkinson, K. D.; Salvesen,711G. S. “Positional-Scanning Fluorogenic Substrate Libraries Reveal Unexpected Specificity712Determinants of Deubiquitinating Enzymes (DUBs)” Biochem. J. 415, 367-375 (2008).

Institution fields

Peer reviewed
yes
First author
Drag
Co-authors
Drag, M.; Mikolajczyk, J.; Bekes, M.; Reyes-Turcu, F.; Ellman, J. A.; Wilkinson, K. D.; Salvesen, G. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Positional-Scanning Fluorogenic Substrate Libraries Reveal Unexpected Specificity Determinants of Deubiquitinating Enzymes (DUBs)Positional-scanning fluorigenic substrate libraries reveal unexpected specificity determinants of DUBs (deubiquitinating enzymes)
year cv 20082008
venue crossref Biochem. J.Biochemical JournalBiochemical Journal
kind cv articleother
DOI crossref 10.1042/bj20080779
first author cv DragDrag

Citations

OpenAlex
none
Scholar
83
DOI
10.1042/bj20080779

Match decisions

  • fingerprint merged · 1.00 · Run 18
2008 Rh(I)-Catalyzed Arylation of Heterocycles via C-H Bond Activation: Expanded Scope Through Mechanistic Insight. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 741–743 · CV · published

741171. Lewis, J. C.; Berman, A. M.; Bergman, R. G.; Ellman, J. A. “Rh(I)-Catalyzed Arylation of742Heterocycles via C-H Bond Activation: Expanded Scope Through Mechanistic Insight.” J. Am.743Chem. Soc. 130, 2493-2500 (2008).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C.; Berman, A. M.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(I)-Catalyzed Arylation of Heterocycles via C-H Bond Activation: Expanded Scope Through Mechanistic Insight.Rh (I)-catalyzed arylation of heterocycles via CH bond activation: Expanded scope through mechanistic insight
year cv 20082008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articleother
DOI crossref 10.1021/ja0748985
first author cv LewisLewis

Citations

OpenAlex
none
Scholar
285
DOI
10.1021/ja0748985

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja0748985 for Rh(I)-catalyzed arylation of heterocycles.
  • fingerprint merged · 1.00 · Run 18
2008 Rh(I)-Catalyzed Direct Arylation of Pyridines and Quinolines Journal of the American Chemical Society article journal CV OA GS

CV span

lines 700–701 · CV · published

700159. Berman, A. M.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A. “Rh(I)-Catalyzed Direct Arylation of701Pyridines and Quinolines” J. Am. Chem. Soc. 130, 14926–14927 (2008).

Institution fields

Peer reviewed
yes
First author
Berman
Co-authors
Berman, A. M.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(I)-Catalyzed Direct Arylation of Pyridines and QuinolinesRh(I)-Catalyzed Direct Arylation of Pyridines and QuinolinesRh (I)-catalyzed direct arylation of pyridines and quinolines
year cv 200820082008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja805939610.1021/ja8059396
first author openalex BermanBermanBerman

Citations

OpenAlex
323
Scholar
345
DOI
10.1021/ja8059396
OpenAlex
W2033753805

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/ja8059396 for rh(i)-catalyzed direct arylation of pyridines and quinolines.
2008 Synthesis of a Benzodiazepine-derived Rhodium NHC Complex by C-H Bond Activation Organometallics article journal CV OA GS

CV span

lines 724–725 · CV · published

724166. Gribble, M. W.; Ellman, J. A.; Bergman, R. G. “Synthesis of a Benzodiazepine-derived Rhodium725NHC Complex by C-H Bond Activation” Organometallics 27, 2152-2155 (2008).

Institution fields

Peer reviewed
yes
First author
Gribble
Co-authors
Gribble, M. W.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Synthesis of a Benzodiazepine-derived Rhodium NHC Complex by C-H Bond ActivationSynthesis of a Benzodiazepine-Derived Rhodium NHC Complex by C−H Bond ActivationSynthesis of a benzodiazepine-derived rhodium NHC complex by CH bond activation
year cv 200820082008
venue crossref OrganometallicsOrganometallicsOrganometallics
kind cv articlearticleother
DOI crossref 10.1021/om800083910.1021/om8000839
first author openalex GribbleGribbleGribble

Citations

OpenAlex
46
Scholar
52
DOI
10.1021/om8000839
OpenAlex
W2058724381

Match decisions

  • doi merged · 1.00 · Run 18
2008 Synthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C-H Activation Journal of the American Chemical Society article CV OA GS needs review

CV span

lines 734–735 · CV · published

734169. Colby, D. A.; Bergman, R. G.; Ellman, J. A. “Synthesis of Dihydropyridines and Pyridines from735Imines and Alkynes via C-H Activation” J. Am. Chem. Soc. 130, 3645-3651 (2008).

Institution fields

Peer reviewed
yes
First author
Colby
Co-authors
Colby, D. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C-H ActivationSynthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C-H ActivationSynthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C−H ActivationThe Synthesis of Dihydropyridines and Pyridines from Imines and Alkynes via CH Activation
year cv 2008200920082008
venue crossref J. Am. Chem. Soc.OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja710478410.1021/ja7104784
first author openalex ColbyEllmanColbyColby

Also recorded as

  • W1995049404 (DOI 10.1021/ja7104784) · same title · 2008 Synthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C−H Activation

Citations

OpenAlex
0
Scholar
438
DOI
10.1021/ja7104784
OpenAlex
W187108596

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja7104784 for the synthesis of dihydropyridines.
  • fingerprint merged · 1.00 · Run 18
2008 The Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C-H Bond Activation/Alkenylation/Electrocyclization Journal of the American Chemical Society article journal CV OA GS

CV span

lines 737–739 · CV · published

737170. Yotphan, S.; Bergman, R. G.; Ellman, J. A. “The Stereoselective Formation of Bicyclic Enamines738with Bridgehead Unsaturation via Tandem C-H Bond Activation/Alkenylation/Electrocyclization”739J. Am. Chem. Soc. 130, 2452-2453 (2008).

Institution fields

Peer reviewed
yes
First author
Yotphan
Co-authors
Yotphan, S.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C-H Bond Activation/Alkenylation/ElectrocyclizationThe Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C−H Bond Activation/Alkenylation/ElectrocyclizationThe Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C-H Bond Activation/Alkenylation/ElectrocyclizationThe stereoselective formation of bicyclic enamines with bridgehead unsaturation via tandem CH bond activation/alkenylation/electrocyclization
year cv 2008200820092008
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyOSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)Journal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja710981b10.1021/ja710981b
first author openalex YotphanYotphanEllmanYotphan

Also recorded as

Citations

OpenAlex
42
Scholar
49
DOI
10.1021/ja710981b
OpenAlex
W2020176610

Match decisions

  • doi merged · 1.00 · Run 18
2007 Asymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C-H Bond Activation Synlett article journal CV OA GS

CV span

lines 758–760 · CV · published

758176. Watzke, A.; Wilson, R. M.; O’Malley, S. J.; Bergman, R. G.; Ellman, J. A. “Asymmetric759Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C-H Bond Activation” Synlett7602383-2389 (2007).

Institution fields

Peer reviewed
yes
First author
Watzke
Co-authors
Watzke, A.; Wilson, R. M.; O’Malley, S. J.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Asymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C-H Bond ActivationAsymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C-H Bond ActivationAsymmetric intramolecular alkylation of chiral aromatic imines via catalytic CH bond activation
year cv 200720072007
venue crossref SynlettSynlettSynlett
kind cv articlearticleother
DOI crossref 10.1055/s-2007-98559310.1055/s-2007-985593
first author openalex WatzkeBergmanWatzke

Citations

OpenAlex
16
Scholar
34
DOI
10.1055/s-2007-985593
OpenAlex
W2025597243

Match decisions

  • doi merged · 1.00 · Run 18
2007 Catalytic Enantioselective Addition of Arylboronic Acids to N-Boc Imines Generated in Situ Organic Letters article journal CV OA GS

CV span

lines 748–749 · CV · published

748173. Nakagawa, H.; Rech, J. C.; Sindelar, R. W.; Ellman, J. A. “Catalytic Enantioselective Addition of749Arylboronic Acids to N-Boc Imines Generated in Situ” Org. Lett. 9, 5155-5157 (2007).

Institution fields

Peer reviewed
yes
First author
Nakagawa
Co-authors
Nakagawa, H.; Rech, J. C.; Sindelar, R. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Addition of Arylboronic Acids to N-Boc Imines Generated in SituCatalytic Enantioselective Addition of Arylboronic Acids to N-Boc Imines Generated in SituCatalytic Enantioselective Addition of Arylboronic Acids to N-Boc Imines Generated in Situ
year cv 200720072007
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol702045w10.1021/ol702045w
first author openalex NakagawaNakagawaNakagawa

Citations

OpenAlex
79
Scholar
79
DOI
10.1021/ol702045w
OpenAlex
W2952698228

Match decisions

  • doi merged · 1.00 · Run 18
2007 Design, Synthesis, and Biological Properties of Highly Potent Tubulysin D Analogues Chemistry – A European Journal article journal CV OA GS needs review

CV span

lines 751–752 · CV · published

751174. Patterson, A. W.; Peltier, H. M.; Sasse, F.; Ellman, J. A. “Design, Synthesis, and Biological752Properties of Highly Potent Tubulysin D Analogues” Chem. Eur. J. 13, 9534-9541 (2007).

Institution fields

Peer reviewed
yes
First author
Patterson
Co-authors
Patterson, A. W.; Peltier, H. M.; Sasse, F.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design, Synthesis, and Biological Properties of Highly Potent Tubulysin D AnaloguesDesign, Synthesis, and Biological Properties of Highly Potent Tubulysin D AnaloguesDesign, synthesis, and biological properties of highly potent tubulysin D analogues
year cv 200720072007
venue crossref Chem. Eur. J.Chemistry - A European JournalChemistry–A European JournalChemistry – A European Journal
kind cv articlearticleother
DOI crossref 10.1002/chem.20070105710.1002/chem.200701057
first author openalex PattersonPattersonPatterson

Citations

OpenAlex
75
Scholar
113
DOI
10.1002/chem.200701057
OpenAlex
W2105144416

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja067177z for total synthesis of tubulysin D.
  • doi merged · 1.00 · Run 18
2007 Enantioselective Aza-Henry Reaction with an N-Sulfinyl Urea Organocatalyst Journal of the American Chemical Society article journal CV OA GS

CV span

lines 745–746 · CV · published

745172. Robak, M. T.; Trincado, M.; Ellman, J. A. “Enantioselective Aza-Henry Reaction with an N-746Sulfinyl Urea Organocatalyst” J. Am. Chem. Soc. 129, 15110-15111 (2007).

Institution fields

Peer reviewed
yes
First author
Robak
Co-authors
Robak, M. T.; Trincado, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Aza-Henry Reaction with an N-Sulfinyl Urea OrganocatalystEnantioselective Aza-Henry Reaction with an N-Sulfinyl Urea OrganocatalystEnantioselective aza-Henry reaction with an N-sulfinyl urea organocatalyst
year cv 200720072007
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja075653v10.1021/ja075653v
first author openalex RobakRobakRobak

Citations

OpenAlex
191
Scholar
250
DOI
10.1021/ja075653v
OpenAlex
W2021825753

Match decisions

  • doi merged · 1.00 · Run 18
2007 Fragment-Based Substrate Activity Screening method for the Identification of Potent Inhibitors of the M. tuberculosis Phosphatase PtpB Journal of the American Chemical Society article journal CV OA GS

CV span

lines 762–765 · CV · published

762177. Soellner, M. B.; Rawles, K. A.; Grundner, C.; Alber, T.; Ellman, J. A. “Fragment-Based Substrate763Activity Screening method for the Identification of Potent Inhibitors of the M. tuberculosis764Phosphatase PtpB” J. Am. Chem. Soc. 129, 9613-9615 (2007) [Research Highlight in Nat. Chem.765Biol. 3, 539 (2007)].

Institution fields

Peer reviewed
yes
First author
Soellner
Co-authors
Soellner, M. B.; Rawles, K. A.; Grundner, C.; Alber, T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Fragment-Based Substrate Activity Screening method for the Identification of Potent Inhibitors of the M. tuberculosis Phosphatase PtpBFragment-Based Substrate Activity Screening Method for the Identification of Potent Inhibitors of the Mycobacterium tuberculosis Phosphatase PtpBFragment-based substrate activity screening method for the identification of potent inhibitors of the Mycobacterium tuberculosis phosphatase PtpB
year cv 200720072007
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja072752010.1021/ja0727520
first author openalex SoellnerSoellnerSoellner

Citations

OpenAlex
107
Scholar
133
DOI
10.1021/ja0727520
OpenAlex
W2011016827

Match decisions

  • doi merged · 1.00 · Run 18
2007 Nonpeptidic Inhibitors of Cathepsin S with an Unprecedented Binding Mode Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 772–774 · CV · published

772180. Inagaki, H.; Tsuruoka, H.; Hornsby, M.; Lesley, S. A.; Spraggon, G.; Ellman, J. A. “Nonpeptidic773Inhibitors of Cathepsin S with an Unprecedented Binding Mode” J. Med. Chem. 50, 2693-2699774(2007).

Institution fields

Peer reviewed
yes
First author
Inagaki
Co-authors
Inagaki, H.; Tsuruoka, H.; Hornsby, M.; Lesley, S. A.; Spraggon, G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Nonpeptidic Inhibitors of Cathepsin S with an Unprecedented Binding ModeCharacterization and Optimization of Selective, Nonpeptidic Inhibitors of Cathepsin S with an Unprecedented Binding ModeCharacterization and optimization of selective, nonpeptidic inhibitors of cathepsin S with an unprecedented binding mode
year cv 200720072007
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm070111+10.1021/jm070111+
first author openalex InagakiInagakiInagaki

Citations

OpenAlex
26
Scholar
41
DOI
10.1021/jm070111+
OpenAlex
W1975820620

Match decisions

  • doi merged · 1.00 · Run 18
2007 One-Pot Asymmetric Synthesis of Either Diastereomer of tert-Butanesulfinyl-protected Amines from Ketones The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 783–785 · CV · published

783183. Tanuwidjaja, J.; Peltier, H. M.; Ellman, J. A. “One-Pot Asymmetric Synthesis of Either784Diastereomer of tert-Butanesulfinyl-protected Amines from Ketones” J. Org. Chem. 72, 626-629785(2007).

Institution fields

Peer reviewed
yes
First author
Tanuwidjaja
Co-authors
Tanuwidjaja, J.; Peltier, H. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv One-Pot Asymmetric Synthesis of Either Diastereomer of tert-Butanesulfinyl-protected Amines from KetonesOne-Pot Asymmetric Synthesis of Either Diastereomer of tert-Butanesulfinyl-protected Amines from KetonesOne‐Pot Asymmetric Synthesis of Either Diastereomer of tert‐Butanesulfinyl‐Protected Amines from Ketones.One-Pot Asymmetric Synthesis of Either Diastereomer of tert-Butanesulfinyl-protected Amines from Ketones
year cv 2007200620072007
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo061651210.1021/jo061651210.1002/chin.200721047
first author openalex TanuwidjajaTanuwidjajaTanuwidjajaTanuwidjaja

Also recorded as

  • W2953293788 (DOI 10.1002/chin.200721047) · same title · 2007 One‐Pot Asymmetric Synthesis of Either Diastereomer of tert‐Butanesulfinyl‐Protected Amines from Ketones.

Citations

OpenAlex
94
Scholar
136
DOI
10.1021/jo0616512
OpenAlex
W2167879129

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2007 One-Pot Microwave-Promoted Synthesis of Nitriles from Aldehydes via tert-Butanesulfinyl Imines Synthesis article journal CV OA GS

CV span

lines 754–756 · CV · published

754175. Tanuwidjaja, J.; Peltier, H. M.; Lewis, J. C.; Schenkel, L. B.; Ellman, J. A. “One-Pot Microwave-755Promoted Synthesis of Nitriles from Aldehydes via tert-Butanesulfinyl Imines” Synthesis 3385-7563389 (2007).

Institution fields

Peer reviewed
yes
First author
Tanuwidjaja
Co-authors
Tanuwidjaja, J.; Peltier, H. M.; Lewis, J. C.; Schenkel, L. B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv One-Pot Microwave-Promoted Synthesis of Nitriles from Aldehydes via tert-Butanesulfinyl IminesOne-Pot Microwave-Promoted Synthesis of Nitriles from Aldehydes via tert -Butanesulfinyl Imines
year cv 20072007
venue crossref SynthesisSynthesis
kind cv articlearticle
DOI crossref 10.1055/s-2007-99080510.1055/s-2007-990805
first author openalex TanuwidjajaEllman

Citations

OpenAlex
3
Scholar
none
DOI
10.1055/s-2007-990805
OpenAlex
W2951907158

Match decisions

  • doi merged · 1.00 · Run 18
2007 Peptide-Nanocrescent Hybrid SERS Probe for Optical Detection of Protease Activity Journal of Nanoscience and Nanotechnology article journal CV OA GS

CV span

lines 787–789 · CV · published

787184. Liu, G. L.; Rosa-Bauza, Y. T.; Salisbury, C. T.; Lu, Y.; Kim, J.; Craik, C.; Ellman, J. A.; Lee, L. P.;788Chen, F. F. "Peptide-Nanocrescent Hybrid SERS Probe for Optical Detection of Protease Activity"789J. Nanoscience Nanotech. 7, 2323–2330 (2007).

Institution fields

Peer reviewed
yes
First author
Liu
Co-authors
Liu, G. L.; Rosa-Bauza, Y. T.; Salisbury, C. T.; Lu, Y.; Kim, J.; Craik, C.; Ellman, J. A.; Lee, L. P.; Chen, F. F.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Peptide-Nanocrescent Hybrid SERS Probe for Optical Detection of Protease ActivityPeptide-Nanoparticle Hybrid SERS Probes for Optical Detection of Protease ActivityPeptide-nanoparticle hybrid SERS probes for optical detection of protease activity
year cv 200720072007
venue crossref J. Nanoscience Nanotech.Journal of Nanoscience and NanotechnologyJournal of nanoscience and nanotechnologyJournal of Nanoscience and Nanotechnology
kind cv articlearticleother
DOI crossref 10.1166/jnn.2007.44410.1166/jnn.2007.444
first author openalex LiuLiuLiu

Citations

OpenAlex
34
Scholar
41
DOI
10.1166/jnn.2007.444
OpenAlex
W2312778997

Match decisions

  • doi merged · 1.00 · Run 18
2007 Rh(I)-Catalyzed Alkylation of Quinolines and Pyridines via C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 776–777 · CV · published

776181. Lewis, J. C.; Bergman, R. G.; Ellman, J. A. “Rh(I)-Catalyzed Alkylation of Quinolines and777Pyridines via C-H Bond Activation” J. Am. Chem. Soc. 129, 5332-5333 (2007).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rh(I)-Catalyzed Alkylation of Quinolines and Pyridines via C-H Bond ActivationRh(I)-Catalyzed Alkylation of Quinolines and Pyridines via C−H Bond ActivationRh(I)‐Catalyzed Alkylation of Quinolines and Pyridines via C—H Bond Activation.Rh (I)-catalyzed alkylation of quinolines and pyridines via CH bond activation
year cv 2007200720072007
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja070388z10.1021/ja070388z10.1002/chin.200737137
first author openalex LewisLewisLewisLewis

Also recorded as

Citations

OpenAlex
348
Scholar
379
DOI
10.1021/ja070388z
OpenAlex
W1995484835

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2007 Straightforward Preparation and Assay of Aspartyl Protease Substrates with an Internal Thioester Linkage ChemBioChem article journal CV OA GS

CV span

lines 767–768 · CV · published

767178. Rosa-Bauza, Y. T.; Berst, F.; Ellman, J. A. “Straightforward Preparation and Assay of Aspartyl768Protease Substrates with an Internal Thioester Linkage” ChemBioChem 8, 981-984 (2007).

Institution fields

Peer reviewed
yes
First author
Rosa-Bauza
Co-authors
Rosa-Bauza, Y. T.; Berst, F.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Straightforward Preparation and Assay of Aspartyl Protease Substrates with an Internal Thioester LinkageStraightforward Preparation and Assay of Aspartyl Protease Substrates with an Internal Thioester Linkage
year cv 20072007
venue crossref ChemBioChemChemBioChem
kind cv articlearticle
DOI crossref 10.1002/cbic.20070000810.1002/cbic.200700008
first author openalex Rosa-BauzaRosa‐Bauzá

Citations

OpenAlex
3
Scholar
none
DOI
10.1002/cbic.200700008
OpenAlex
W2126995115

Match decisions

  • doi merged · 1.00 · Run 18
2007 Substrate Activity Acreening (SAS): a General Procedure for the Preparation and Screening of a Fragment-based Non-peptidic Protease Substrate Library for Inhibitor Discovery Nature Protocols article journal CV OA GS

CV span

lines 795–797 · CV · published

795186. Patterson, A. W.; Wood, W. J. L.; Ellman, J. A. “Substrate Activity Acreening (SAS): a General796Procedure for the Preparation and Screening of a Fragment-based Non-peptidic Protease Substrate797Library for Inhibitor Discovery” Nat. Protoc. 2, 424 - 433 (2007).

Institution fields

Peer reviewed
yes
First author
Patterson
Co-authors
Patterson, A. W.; Wood, W. J. L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Substrate Activity Acreening (SAS): a General Procedure for the Preparation and Screening of a Fragment-based Non-peptidic Protease Substrate Library for Inhibitor DiscoverySubstrate activity screening (SAS): a general procedure for the preparation and screening of a fragment-based non-peptidic protease substrate library for inhibitor discoverySubstrate activity screening (SAS): a general procedure for the preparation and screening of a fragment-based non-peptidic protease substrate library for inhibitor discovery
year cv 200720072007
venue crossref Nat. Protoc.Nature ProtocolsNature protocolsNature Protocols
kind cv articlearticleother
DOI crossref 10.1038/nprot.2007.2810.1038/nprot.2007.28
first author openalex PattersonPattersonPatterson

Citations

OpenAlex
33
Scholar
47
DOI
10.1038/nprot.2007.28
OpenAlex
W2088944010

Match decisions

  • doi merged · 1.00 · Run 18
2007 Synthesis of Potent Bicyclic Bisarylimidazole c-Jun N-Terminal Kinase Inhibitors by Catalytic C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 779–781 · CV · published

779182. Rech, J. C.; Yato, M.; Duckett, D.; Ember, Brian; LoGrasso, P. V.; Bergman, R. G.; Ellman, J. A.780“Synthesis of Potent Bicyclic Bisarylimidazole c-Jun N-Terminal Kinase Inhibitors by Catalytic C-781H Bond Activation” J. Am. Chem. Soc. 129, 490-491 (2007).

Institution fields

Peer reviewed
yes
First author
Rech
Co-authors
Rech, J. C.; Yato, M.; Duckett, D.; Ember, Brian; LoGrasso, P. V.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of Potent Bicyclic Bisarylimidazole c-Jun N-Terminal Kinase Inhibitors by Catalytic C-H Bond ActivationSynthesis of Potent Bicyclic Bisarylimidazole c-Jun N-Terminal Kinase Inhibitors by Catalytic C−H Bond ActivationSynthesis of potent bicyclic bis-arylimidazole c-Jun N-terminal kinase inhibitors by catalytic CH bond activation
year cv 200720062007
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja067600410.1021/ja0676004
first author openalex RechRechRech

Citations

OpenAlex
102
Scholar
117
DOI
10.1021/ja0676004
OpenAlex
W2042388537

Match decisions

  • doi merged · 1.00 · Run 18
2007 The Direct Approach Science article journal CV OA GS

CV span

lines 770–770 · CV · published

770179. Ellman, J. A. “The Direct Approach” Science 316, 1131-1132 (2007).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv The Direct ApproachThe Direct ApproachThe direct approach
year cv 200720072007
venue crossref ScienceScienceScience
kind cv articlearticleother
DOI crossref 10.1126/science.114337310.1126/science.1143373
first author openalex EllmanEllmanEllman

Citations

OpenAlex
39
Scholar
27
DOI
10.1126/science.1143373
OpenAlex
W1521715129

Match decisions

  • doi merged · 1.00 · Run 18
2006 Asymmetric Synthesis of ,-Dibranched Propargylamines by Acetylide Additions to N-tert-Butanesulfinyl Ketimines The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 807–809 · CV · published

807189. Patterson, A. W.; Ellman, J. A. “Asymmetric Synthesis of ,-Dibranched Propargylamines by808Acetylide Additions to N-tert-Butanesulfinyl Ketimines” J. Org. Chem. 71, 7110-7112 (2006).809

Institution fields

Peer reviewed
yes
First author
Patterson
Co-authors
Patterson, A. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of ,-Dibranched Propargylamines by Acetylide Additions to N-tert-Butanesulfinyl KetiminesAsymmetric Synthesis of α,α-Dibranched Propargylamines by Acetylide Additions to N-tert-Butanesulfinyl KetiminesAsymmetric Synthesis of α,α‐Dibranched Propargylamines by Acetylide Additions to N‐tert‐Butanesulfinyl Ketimines.Asymmetric Synthesis of α,α-Dibranched Propargylamines by Acetylide Additions to N-tert-Butanesulfinyl Ketimines
year cv 2006200620062006
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo061160h10.1021/jo061160h10.1002/chin.200701065
first author openalex PattersonPattersonPattersonPatterson

Also recorded as

  • W2949238499 (DOI 10.1002/chin.200701065) · same title · 2006 Asymmetric Synthesis of α,α‐Dibranched Propargylamines by Acetylide Additions to N‐tert‐Butanesulfinyl Ketimines.

Citations

OpenAlex
55
Scholar
68
DOI
10.1021/jo061160h
OpenAlex
W2105379367

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo061160h for propargylamines synthesis.
  • doi merged · 1.00 · Run 18
2006 Asymmetric Synthesis of Protected Arylglycines by Rhodium-Catalyzed Addition of Arylboronic Acids to N-tert-Butanesulfinyl Imino Esters Journal of the American Chemical Society article journal CV OA GS

CV span

lines 827–829 · CV · published

827195. Beenen, M. A.; Weix, D. J.; Ellman, J. A. “Asymmetric Synthesis of Protected Arylglycines by828Rhodium-Catalyzed Addition of Arylboronic Acids to N-tert-Butanesulfinyl Imino Esters” J. Am.829Chem. Soc. 128, 6304-6305 (2006).

Institution fields

Peer reviewed
yes
First author
Beenen
Co-authors
Beenen, M. A.; Weix, D. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Protected Arylglycines by Rhodium-Catalyzed Addition of Arylboronic Acids to N-tert-Butanesulfinyl Imino EstersAsymmetric Synthesis of Protected Arylglycines by Rhodium-Catalyzed Addition of Arylboronic Acids to N-tert-Butanesulfinyl Imino EstersAsymmetric Synthesis of Protected Arylglycines by Rhodium‐Catalyzed Addition of Arylboronic Acids to N‐tert‐Butanesulfinyl Imino Esters.Asymmetric synthesis of protected arylglycines by rhodium-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters
year cv 2006200620062006
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja060529h10.1021/ja060529h10.1002/chin.200639208
first author openalex BeenenBeenenBeenenBeenen

Also recorded as

  • W2952045446 (DOI 10.1002/chin.200639208) · same title · 2006 Asymmetric Synthesis of Protected Arylglycines by Rhodium‐Catalyzed Addition of Arylboronic Acids to N‐tert‐Butanesulfinyl Imino Esters.

Citations

OpenAlex
137
Scholar
166
DOI
10.1021/ja060529h
OpenAlex
W2159292003

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2006 Enantioselective Synthesis of a PKC Inhibitor via Catalytic C-H Bond Activation Organic Letters article journal CV OA GS

CV span

lines 824–825 · CV · published

824194. Wilson, R. M.; Thalji, R. K.; Bergman, R. G.; Ellman, J. A. “Enantioselective Synthesis of a PKC825Inhibitor via Catalytic C-H Bond Activation” Org. Lett. 8, 1745-1747 (2006).

Institution fields

Peer reviewed
yes
First author
Wilson
Co-authors
Wilson, R. M.; Thalji, R. K.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Synthesis of a PKC Inhibitor via Catalytic C-H Bond ActivationEnantioselective Synthesis of a PKC Inhibitor via Catalytic C−H Bond ActivationEnantioselective synthesis of a PKC inhibitor via catalytic C− H bond activation
year cv 200620062006
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol060485h10.1021/ol060485h
first author openalex WilsonWilsonWilson

Citations

OpenAlex
149
Scholar
174
DOI
10.1021/ol060485h
OpenAlex
W2041218412

Match decisions

  • doi merged · 1.00 · Run 18
2006 Experimental and Computational Studies on the Mechanism of N-Heterocycle C-H Activation by Rh(I) Journal of the American Chemical Society article journal CV OA GS

CV span

lines 838–840 · CV · published

838198. Wiedemann, S. H.; Lewis, J. C.; Ellman, J. A.; Bergman, R. G. “Experimental and Computational839Studies on the Mechanism of N-Heterocycle C-H Activation by Rh(I)” J. Am. Chem. Soc. 128,8402452-2462 (2006).

Institution fields

Peer reviewed
yes
First author
Wiedemann
Co-authors
Wiedemann, S. H.; Lewis, J. C.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Experimental and Computational Studies on the Mechanism of N-Heterocycle C-H Activation by Rh(I)Experimental and Computational Studies on the Mechanism ofN-Heterocycle C−H Activation by Rh(I)Experimental and Computational Studies on the Mechanism of N-Heterocycle CH Activation by Rh (I)/PCy3
year cv 200620062006
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja057668410.1021/ja0576684
first author openalex WiedemannWiedemannWiedemann

Citations

OpenAlex
194
Scholar
220
DOI
10.1021/ja0576684
OpenAlex
W2042481895

Match decisions

  • doi merged · 1.00 · Run 18
2006 Functional Phenotyping of Human Plasma Using a 361-Fluorogenic Substrate Biosensing Microarray Biotechnology and Bioengineering article journal CV OA GS

CV span

lines 820–822 · CV · published

820193. Gosalia, D. N.; Denney, W. S.; Salisbury, C. M.; Ellman, J. A.; Diamond, S. L. “Functional821Phenotyping of Human Plasma Using a 361-Fluorogenic Substrate Biosensing Microarray”822Biotechnol. Bioeng. 94, 1099-1110 (2006).

Institution fields

Peer reviewed
yes
First author
Gosalia
Co-authors
Gosalia, D. N.; Denney, W. S.; Salisbury, C. M.; Ellman, J. A.; Diamond, S. L.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Functional Phenotyping of Human Plasma Using a 361-Fluorogenic Substrate Biosensing MicroarrayFunctional phenotyping of human plasma using a 361‐fluorogenic substrate biosensing microarrayFunctional phenotyping of human plasma using a 361‐fluorogenic substrate biosensing microarray
year cv 200620062006
venue crossref Biotechnol. Bioeng.Biotechnology and BioengineeringBiotechnology and bioengineeringBiotechnology and Bioengineering
kind cv articlearticleother
DOI crossref 10.1002/bit.2092710.1002/bit.20927
first author openalex GosaliaGosaliaGosalia

Citations

OpenAlex
29
Scholar
35
DOI
10.1002/bit.20927
OpenAlex
W2147022417

Match decisions

  • doi merged · 1.00 · Run 18
2006 Identification of Selective, Nonpeptidic Nitrile Inhibitors of Cathepsin S using the Substrate Activity Screening Method Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 799–801 · CV · published

799187. Patterson, A. W.; Wood, W. J. L.; Hornsby, M.; Lesley, S.; Spraggon, G.; Ellman, J. A.800“Identification of Selective, Nonpeptidic Nitrile Inhibitors of Cathepsin S using the Substrate801Activity Screening Method” J. Med. Chem. 49, 6298-6307 (2006).

Institution fields

Peer reviewed
yes
First author
Patterson
Co-authors
Patterson, A. W.; Wood, W. J. L.; Hornsby, M.; Lesley, S.; Spraggon, G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of Selective, Nonpeptidic Nitrile Inhibitors of Cathepsin S using the Substrate Activity Screening MethodIdentification of Selective, Nonpeptidic Nitrile Inhibitors of Cathepsin S Using the Substrate Activity Screening MethodIdentification of selective, nonpeptidic nitrile inhibitors of cathepsin S using the substrate activity screening method
year cv 200620062006
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm060701s10.1021/jm060701s
first author openalex PattersonPattersonPatterson

Citations

OpenAlex
86
Scholar
115
DOI
10.1021/jm060701s
OpenAlex
W2056960294

Match decisions

  • doi merged · 1.00 · Run 18
2006 Microwave-Promoted Rhodium-Catalyzed Arylation of Heterocycles through CH Bond Activation Angewandte Chemie International Edition version 2006 Microwave‐Promoted Rhodium‐Catalyzed Arylation of Heterocycles Through C—H Bond Activatio… article journal CV OA GS needs review

CV span

lines 834–836 · CV · published

834197. Lewis, J. C.; Wu, J. Y.; Ellman, J. A.; Bergman, R. G. “Microwave-Promoted Rhodium-Catalyzed835Arylation of Heterocycles through CH Bond Activation” Angew. Chem. Int. Ed. 45, 1589-1591836(2006).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C.; Wu, J. Y.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Microwave-Promoted Rhodium-Catalyzed Arylation of Heterocycles through CH Bond ActivationMicrowave‐Promoted Rhodium‐Catalyzed Arylation of Heterocycles through CH Bond ActivationMicrowave‐Promoted Rhodium‐Catalyzed Arylation of Heterocycles through CH Bond Activation
year cv 200620062006
venue crossref Angew. Chem. Int. Ed.Angewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticle
DOI crossref 10.1002/anie.20050428910.1002/anie.20050428910.1002/ange.200504289
first author openalex LewisLewisLewis

Also recorded as

Citations

OpenAlex
138
Scholar
none
Scholar with related records
172
DOI
10.1002/anie.200504289
OpenAlex
W2108718491

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/anie.200504289 for microwave-promoted rhodium-catalyzed arylation.
  • doi merged · 1.00 · Run 18
2006 NMR Shifts, Orbitals, and M···H-X Bonding in d8 Square Planar Metal Complexes Organometallics article journal CV OA GS

CV span

lines 813–814 · CV · published

813191. Zhang, Y.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A.; Oldfield, E. “NMR Shifts, Orbitals, and814M···H-X Bonding in d8 Square Planar Metal Complexes” Organometallics 25, 3515-3519 (2006).

Institution fields

Peer reviewed
yes
First author
Zhang
Co-authors
Zhang, Y.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A.; Oldfield, E.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv NMR Shifts, Orbitals, and M···H-X Bonding in d8 Square Planar Metal ComplexesNMR Shifts, Orbitals, and M···H−X Bonding in d8 Square Planar Metal ComplexesNMR Shifts, Orbitals, and M···H−X Bonding in d8 Square Planar Metal Complexes
year cv 200620062006
venue crossref OrganometallicsOrganometallicsOrganometallics
kind cv articlearticleother
DOI crossref 10.1021/om060163h10.1021/om060163h
first author openalex ZhangZhangZhang

Citations

OpenAlex
159
Scholar
199
DOI
10.1021/om060163h
OpenAlex
W2051815905

Match decisions

  • doi merged · 1.00 · Run 18
2006 Rapid Identification of Potent Nonpeptidic Serine Protease Inhibitors ChemBioChem article journal CV OA GS

CV span

lines 810–811 · CV · published

810190. Salisbury, C. M.; Ellman, J. A. “Rapid Identification of Potent Nonpeptidic Serine Protease811Inhibitors” ChemBioChem 7, 1034-1037 (2006).

Institution fields

Peer reviewed
yes
First author
Salisbury
Co-authors
Salisbury, C. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Rapid Identification of Potent Nonpeptidic Serine Protease InhibitorsRapid Identification of Potent Nonpeptidic Serine Protease InhibitorsRapid identification of potent nonpeptidic serine protease inhibitors
year cv 200620062006
venue crossref ChemBioChemChemBioChemChemBioChem
kind cv articlearticleother
DOI crossref 10.1002/cbic.20060008110.1002/cbic.200600081
first author openalex SalisburySalisburySalisbury

Citations

OpenAlex
23
Scholar
29
DOI
10.1002/cbic.200600081
OpenAlex
W2073962207

Match decisions

  • doi merged · 1.00 · Run 18
2006 Reassignment of Configuration for Salvianolic Acid B and Establishment of Its Identity with Lithospermic Acid B Journal of Natural Products article journal CV OA GS

CV span

lines 803–805 · CV · published

803188. Watzke, A.; O’Malley, S. J.; Bergman, R. G.; Ellman, J. A. “Reassignment of Configuration for804Salvianolic Acid B and Establishment of Its Identity with Lithospermic Acid B” J. Nat. Prod. 69,8051231-1233 (2006).

Institution fields

Peer reviewed
yes
First author
Watzke
Co-authors
Watzke, A.; O’Malley, S. J.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Reassignment of Configuration for Salvianolic Acid B and Establishment of Its Identity with Lithospermic Acid BReassignment of the Configuration of Salvianolic Acid B and Establishment of Its Identity with Lithospermic Acid BReassignment of the configuration of salvianolic acid B and establishment of its identity with lithospermic acid B
year cv 200620062006
venue crossref J. Nat. Prod.Journal of Natural ProductsJournal of Natural ProductsJournal of Natural Products
kind cv articlearticleother
DOI crossref 10.1021/np060136w10.1021/np060136w
first author openalex WatzkeWatzkeWatzke

Citations

OpenAlex
63
Scholar
76
DOI
10.1021/np060136w
OpenAlex
W2122538212

Match decisions

  • doi merged · 1.00 · Run 18
2006 Rhodium-Catalyzed Direct C-H Addition of 3,4-Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of Vasicoline The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 842–844 · CV · published

842199. Wiedemann, S. H.; Ellman, J. A.; Bergman, R. G. “Rhodium-Catalyzed Direct C-H Addition of8433,4-Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of Vasicoline” J. Org.844Chem. 71, 1969-1976 (2006).

Institution fields

Peer reviewed
yes
First author
Wiedemann
Co-authors
Wiedemann, S. H.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed Direct C-H Addition of 3,4-Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of VasicolineRhodium-Catalyzed Direct C−H Addition of 3,4-Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of VasicolineRhodium‐Catalyzed Direct C—H Addition of 3,4‐Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of Vasicoline.Rhodium-Catalyzed Direct C− H Addition of 3, 4-Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of Vasicoline
year cv 2006200620062006
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo052345b10.1021/jo052345b10.1002/chin.200629147
first author openalex WiedemannWiedemannWiedemannWiedemann

Also recorded as

  • W2949206990 (DOI 10.1002/chin.200629147) · same title · 2006 Rhodium‐Catalyzed Direct C—H Addition of 3,4‐Dihydroquinazolines to Alkenes and Their Use in the Total Synthesis of Vasicoline.

Citations

OpenAlex
81
Scholar
97
DOI
10.1021/jo052345b
OpenAlex
W2176041069

Match decisions

  • passthrough_guard not merged · 0.80 · low_confidence · Run 18 Group contains two distinct papers by Wiedemann and Ellman on oxazolines and dihydroquinazolines via rhodium catalysis, likely mixed due to related methodology.
  • doi merged · 1.00 · Run 18
2006 Stereoselective Alkylation of α,-Unsaturated Imines via C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 831–832 · CV · published

831196. Colby, D. A.; Bergman, R. G.; Ellman, J. A. “Stereoselective Alkylation of α,-Unsaturated Imines832via C-H Bond Activation” J. Am. Chem. Soc. 128, 5604-05 (2006).

Institution fields

Peer reviewed
yes
First author
Colby
Co-authors
Colby, D. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Stereoselective Alkylation of α,-Unsaturated Imines via C-H Bond ActivationStereoselective Alkylation of α,β-Unsaturated Imines via C−H Bond ActivationStereoselective Alkylation of α,β‐Unsaturated Imines via C—H Bond Activation.Stereoselective alkylation of α, β-unsaturated imines via CH bond activation
year cv 2006200620062006
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja058493110.1021/ja058493110.1002/chin.200638063
first author openalex ColbyColbyColbyColby

Also recorded as

Citations

OpenAlex
126
Scholar
144
DOI
10.1021/ja0584931
OpenAlex
W1985521053

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2006 Substrate Profiling of Cysteine Proteases Using a Combinatorial Peptide Library Identifies Functionally Unique Specificities Journal of Biological Chemistry article journal CV OA GS

CV span

lines 816–818 · CV · published

816192. Choe, Y.; Leonetti, F.; Greenbaum, D. C.; Lecaille, F.; Bogyo, M.; Bromme, D.; Ellman, J. A.;817Craik, C. S. “Substrate Profiling of Cysteine Proteases Using a Combinatorial Peptide Library818Identifies Functionally Unique Specificities” J. Biol. Chem. 281, 12824 - 12832 (2006).

Institution fields

Peer reviewed
yes
First author
Choe
Co-authors
Choe, Y.; Leonetti, F.; Greenbaum, D. C.; Lecaille, F.; Bogyo, M.; Bromme, D.; Ellman, J. A.; Craik, C. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Substrate Profiling of Cysteine Proteases Using a Combinatorial Peptide Library Identifies Functionally Unique SpecificitiesSubstrate Profiling of Cysteine Proteases Using a Combinatorial Peptide Library Identifies FunctionallySubstrate profiling of cysteine proteases using a combinatorial peptide library identifies functionally unique specificities
year cv 200620062006
venue crossref J. Biol. Chem.Journal of Biological ChemistryJournal of Biological Chemistry
kind cv articlearticleother
DOI crossref 10.1074/jbc.m513331200
first author openalex ChoeChoeChoe

Citations

OpenAlex
0
Scholar
561
DOI
10.1074/jbc.m513331200
OpenAlex
W2184740999

Match decisions

  • fingerprint merged · 1.00 · Run 18
2006 The Total Synthesis of Tubulysin D Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 791–793 · CV · published

791185. Peltier, H. M.; McMahon, J. P.; Patterson, A. W.; Ellman, J. A. “The Total Synthesis of Tubulysin792D” J. Am. Chem. Soc. 128, 16018-16019 (2006). Critique: Sasse, F.; Menche, D. “Success in793Tubulysin D Synthesis” Nat. Chem. Biol. 3, 87-89 (2007).

Institution fields

Peer reviewed
yes
First author
Peltier
Co-authors
Peltier, H. M.; McMahon, J. P.; Patterson, A. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Total Synthesis of Tubulysin DThe Total Synthesis of Tubulysin DThe Total Synthesis of Tubulysin D (I).The total synthesis of tubulysin D
year cv 2006200620072006
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja067177z10.1021/ja067177z10.1002/chin.200719171
first author openalex PeltierPeltierPeltierPeltier

Also recorded as

Citations

OpenAlex
127
Scholar
185
DOI
10.1021/ja067177z
OpenAlex
W1988236688

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja067177z for total synthesis of tubulysin D.
  • doi merged · 1.00 · Run 18
2005 (+)-2-Methyl-2-propanesulfinamide Organic Syntheses article journal CV OA GS

CV span

lines 854–854 · CV · published

854202. Weix, D. J.; Ellman, J. A. “(+)-2-Methyl-2-propanesulfinamide” Org. Synth. 82, 157-165 (2005).

Institution fields

Peer reviewed
yes
First author
Weix
Co-authors
Weix, D. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv (+)-2-Methyl-2-propanesulfinamide( R S )‐(+)‐2‐Methyl‐2‐propanesulfinamide
year cv 20052005
venue openalex Org. Synth.Organic Syntheses
kind cv articleother
DOI openalex 10.1002/0471264229.os082.24
first author openalex WeixWeix

Citations

OpenAlex
10
Scholar
none
DOI
10.1002/0471264229.os082.24
OpenAlex
W1660162224

Match decisions

  • fingerprint merged · 1.00 · Run 18
2005 Annulation of Aromatic Imines via Directed C-H Bond Activation The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 867–868 · CV · published

867206. Thalji, R. K.; Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A. “Annulation of Aromatic Imines via868Directed C-H Bond Activation” J. Org. Chem. 70, 6775-6781 (2005).

Institution fields

Peer reviewed
yes
First author
Thalji
Co-authors
Thalji, R. K.; Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Annulation of Aromatic Imines via Directed C-H Bond ActivationAnnulation of Aromatic Imines via Directed C−H Bond ActivationAnnulation of Aromatic Imines via Directed C—H Bond Activation.Annulation of aromatic imines via directed C− H bond activation
year cv 2005200520052005
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo050757e10.1021/jo050757e10.1002/chin.200552027
first author openalex ThaljiThaljiThaljiThalji

Also recorded as

Citations

OpenAlex
93
Scholar
113
DOI
10.1021/jo050757e
OpenAlex
W2178468310

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 A Rapid and General Method for the Asymmetric Synthesis of 2-Substituted Pyrrolidines Using tert-Butanesulfinamide Organic & Biomolecular Chemistry article journal CV OA GS

CV span

lines 870–871 · CV · published

870207. Brinner, K. M.; Ellman, J. A. “A Rapid and General Method for the Asymmetric Synthesis of 2-871Substituted Pyrrolidines Using tert-Butanesulfinamide” Org. Biomol. Chem. 3, 2109-2113 (2005).

Institution fields

Peer reviewed
yes
First author
Brinner
Co-authors
Brinner, K. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Rapid and General Method for the Asymmetric Synthesis of 2-Substituted Pyrrolidines Using tert-ButanesulfinamideA rapid and general method for the asymmetric synthesis of 2-substituted pyrrolidines using tert-butanesulfinamideA rapid and general method for the asymmetric synthesis of 2-substituted pyrrolidines using tert-butanesulfinamide
year cv 200520052005
venue crossref Org. Biomol. Chem.Organic & Biomolecular ChemistryOrganic & Biomolecular ChemistryOrganic & Biomolecular Chemistry
kind cv articlearticleother
DOI crossref 10.1039/b502080h10.1039/b502080h
first author openalex BrinnerBrinnerBrinner

Citations

OpenAlex
62
Scholar
80
DOI
10.1039/b502080h
OpenAlex
W2004120839

Match decisions

  • doi merged · 1.00 · Run 18
2005 Asymmetric Conjugate Addition of Copper Reagents to ,-Unsaturated tert-Butanesulfinyl Imines Organic Letters article journal CV OA GS

CV span

lines 851–852 · CV · published

851201. McMahon, J. P.; Ellman, J. A. “Asymmetric Conjugate Addition of Copper Reagents to ,-852Unsaturated tert-Butanesulfinyl Imines” Org. Lett. 7, 5393-5396 (2005).

Institution fields

Peer reviewed
yes
First author
McMahon
Co-authors
McMahon, J. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Conjugate Addition of Copper Reagents to ,-Unsaturated tert-Butanesulfinyl IminesAsymmetric Conjugate Addition of Copper Reagents to α,β-Unsaturated tert-Butanesulfinyl IminesAsymmetric Conjugate Addition of Copper Reagents to α,β‐Unsaturated tert‐Butanesulfinyl Imines.Asymmetric Conjugate Addition of Copper Reagents to α,β-Unsaturated tert-Butanesulfinyl Imines
year cv 2005200520062005
venue crossref Org. Lett.Organic LettersChemInformOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol051986q10.1021/ol051986q10.1002/chin.200613078
first author openalex McMahonMcMahonMcMahonMcMahon

Also recorded as

  • W2952461142 (DOI 10.1002/chin.200613078) · same title · 2006 Asymmetric Conjugate Addition of Copper Reagents to α,β‐Unsaturated tert‐Butanesulfinyl Imines.

Citations

OpenAlex
46
Scholar
61
DOI
10.1021/ol051986q
OpenAlex
W1983658139

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 Asymmetric Synthesis of -Amino Acids by Enolate Additions to tert-Butanesulfinyl Imines Enantioselective Synthesis of β-Amino Acids chapter CV OA GS needs review

CV span

lines 888–890 · CV · published

888212. Brinner, K.; Ellman, J. A. Asymmetric Synthesis of -Amino Acids by Enolate Additions to tert-889Butanesulfinyl Imines. In Enantioselective Synthesis of -Amino Acids, 2nd Edition; Juaristi, E.,890Soloshonok, V., Eds.; John Wiley & Sons, Hoboken, NJ; pp 181-194 (2005).

Institution fields

Peer reviewed
none
First author
Brinner
Co-authors
Brinner, K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
John Wiley & Sons
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of -Amino Acids by Enolate Additions to tert-Butanesulfinyl IminesAsymmetric Synthesis of β-Amino Acids by Enolate Additions to tert-Butanesulfinyl IminesAsymmetric Synthesis of β‐Amino Acids by Enolate Additions to tert‐Butanesulfinyl Imines
year cv 200520052006
venue crossref Enantioselective Synthesis of -Amino Acids, 2nd EditionChemInformEnantioselective Synthesis of β-Amino Acids
kind cv chapterchapterarticle
DOI crossref 10.1002/0471698482.ch810.1002/0471698482.ch810.1002/chin.200629248
first author openalex BrinnerBrinnerBrinner

Also recorded as

Citations

OpenAlex
1
Scholar
none
DOI
10.1002/0471698482.ch8
OpenAlex
W2087913898

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo061160h for propargylamines synthesis.
  • doi merged · 1.00 · Run 18
2005 Catalytic Enantioselective Sulfinyl Transfer Using Cinchona Alkaloid Catalysts Organic Letters article journal CV OA GS

CV span

lines 885–886 · CV · published

885211. Peltier, H. M.; Evans, J. W.; Ellman, J. A. “Catalytic Enantioselective Sulfinyl Transfer Using886Cinchona Alkaloid Catalysts” Org. Lett. 7, 1733-1736 (2005).

Institution fields

Peer reviewed
yes
First author
Peltier
Co-authors
Peltier, H. M.; Evans, J. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Sulfinyl Transfer Using Cinchona Alkaloid CatalystsCatalytic Enantioselective Sulfinyl Transfer Using Cinchona Alkaloid Catalysts.Catalytic Enantioselective Sulfinyl Transfer Using Cinchona Alkaloid CatalystsCatalytic enantioselective sulfinyl transfer using cinchona alkaloid catalysts
year cv 2005200520052005
venue crossref Org. Lett.ChemInformOrganic LettersOrganic lettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol050275p10.1002/chin.20053807610.1021/ol050275p
first author openalex PeltierPeltierPeltierPeltier

Also recorded as

Citations

OpenAlex
52
Scholar
68
DOI
10.1021/ol050275p
OpenAlex
W2949634703

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 Catalytic Functionalization of N-Heterocycles via their Rhodium-Carbene Complexes Handbook of C-H Transformations chapter CV OA GS

CV span

lines 877–879 · CV · published

877209. Wiedemann, S. H.; Ellman, J. A.; Bergman, R. G. Catalytic Functionalization of N-Heterocycles878via their Rhodium-Carbene Complexes. In Handbook of C-H Transformations; Dyker, G., Ed.:879Wiley-VCH Verlag GmbH & Co. KGaA; Weinheim, 187-193 (2005).

Institution fields

Peer reviewed
none
First author
Wiedemann
Co-authors
Wiedemann, S. H.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
Wiley-VCH Verlag GmbH & Co. KGaA
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Catalytic Functionalization of N-Heterocycles via their Rhodium-Carbene Complexes
year cv 2005
venue cv Handbook of C-H Transformations
kind cv chapter
first author cv Wiedemann

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2005 Diastereoselective and Enantioselective Rh(I)-Catalyzed Additions of Arylboronic Acids to N-tert-Butanesulfinyl and N-Diphenylphosphinoyl Aldimines Journal of the American Chemical Society article journal CV OA GS

CV span

lines 895–897 · CV · published

895214. Weix, D. J.; Shi, Y.; Ellman, J. A. “Diastereoselective and Enantioselective Rh(I)-Catalyzed896Additions of Arylboronic Acids to N-tert-Butanesulfinyl and N-Diphenylphosphinoyl Aldimines” J.897Am. Chem. Soc. 127, 1092-1093 (2005).

Institution fields

Peer reviewed
yes
First author
Weix
Co-authors
Weix, D. J.; Shi, Y.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Diastereoselective and Enantioselective Rh(I)-Catalyzed Additions of Arylboronic Acids to N-tert-Butanesulfinyl and N-Diphenylphosphinoyl AldiminesDiastereoselective and Enantioselective Rh(I)-Catalyzed Additions of Arylboronic Acids to N-tert-Butanesulfinyl and N-Diphenylphosphinoyl AldiminesDiastereoselective and Enantioselective Rh(I)‐Catalyzed Additions of Arylboronic Acids to N‐tert‐Butanesulfinyl and N‐Diphenylphosphinoyl Aldimines.Diastereoselective and enantioselective Rh (I)-catalyzed additions of arylboronic acids to N-tert-butanesulfinyl and N-diphenylphosphinoyl aldimines
year cv 2005200520052005
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja044003d10.1021/ja044003d10.1002/chin.200524078
first author openalex WeixWeixWeixWeix

Also recorded as

  • W2949242226 (DOI 10.1002/chin.200524078) · same title · 2005 Diastereoselective and Enantioselective Rh(I)‐Catalyzed Additions of Arylboronic Acids to N‐tert‐Butanesulfinyl and N‐Diphenylphosphinoyl Aldimines.

Citations

OpenAlex
192
Scholar
239
DOI
10.1021/ja044003d
OpenAlex
W2043177113

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 High Throughput Substrate Specificity Profiling of Serine and Cysteine Proteases Using Solution-Phase Fluorogenic Peptide Microarays Molecular & Cellular Proteomics article journal CV OA GS needs review

CV span

lines 881–883 · CV · published

881210. Gosalia, D. N.; Salisbury, C. M.; Ellman, J. A.; Diamond, S. L. “High Throughput Substrate882Specificity Profiling of Serine and Cysteine Proteases Using Solution-Phase Fluorogenic Peptide883Microarays” Molec. Cell. Proteomics 4, 626-636 (2005).

Institution fields

Peer reviewed
yes
First author
Gosalia
Co-authors
Gosalia, D. N.; Salisbury, C. M.; Ellman, J. A.; Diamond, S. L.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv High Throughput Substrate Specificity Profiling of Serine and Cysteine Proteases Using Solution-Phase Fluorogenic Peptide MicroaraysHigh throughput substrate specificity profiling of serine and cysteine proteases using solution-phase fluorogenic peptide microarrays
year cv 20052005
venue crossref Molec. Cell. ProteomicsMolecular & Cellular ProteomicsMolecular & Cellular Proteomics
kind cv articleother
DOI crossref 10.1074/mcp.m500004-mcp200
first author cv GosaliaGosalia

Citations

OpenAlex
none
Scholar
192
DOI
10.1074/mcp.m500004-mcp200

Match decisions

  • passthrough_guard not merged · 0.90 · doi_conflict · Run 18 Records describe the same high throughput specificity profiling of proteases using peptide microarrays across slightly different journal manifestations.
  • fingerprint merged · 1.00 · Run 18
2005 N-Sulfinyl Metalloenamine Conjugate Additions: Asymmetric Synthesis of Piperidines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 864–865 · CV · published

864205. Peltier, H. M.; Ellman, J. A. “N-Sulfinyl Metalloenamine Conjugate Additions: Asymmetric865Synthesis of Piperidines” J. Org. Chem. 70, 7342-7345 (2005).

Institution fields

Peer reviewed
yes
First author
Peltier
Co-authors
Peltier, H. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv N-Sulfinyl Metalloenamine Conjugate Additions: Asymmetric Synthesis of PiperidinesN -Sulfinyl Metalloenamine Conjugate Additions: Asymmetric Synthesis of PiperidinesN‐Sulfinyl Metalloenamine Conjugate Additions: Asymmetric Synthesis of Piperidines.N-Sulfinyl Metalloenamine Conjugate Additions: Asymmetric Synthesis of Piperidines
year cv 2005200520052005
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo051020s10.1021/jo051020s10.1002/chin.200601065
first author openalex PeltierPeltierPeltierPeltier

Also recorded as

Citations

OpenAlex
54
Scholar
65
DOI
10.1021/jo051020s
OpenAlex
W2107387898

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 Potent 4-Aminopiperidine Based Antimalarial Agents Bioorganic & Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 892–893 · CV · published

892213. Brinner, K. M.; Powles, M. A.; Schmatz, D. M.; Ellman, J. A. “Potent 4-Aminopiperidine Based893Antimalarial Agents” Bioorg. Med. Chem. Lett. 15, 345-348 (2005).

Institution fields

Peer reviewed
yes
First author
Brinner
Co-authors
Brinner, K. M.; Powles, M. A.; Schmatz, D. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Potent 4-Aminopiperidine Based Antimalarial AgentsPotent 4-aminopiperidine based antimalarial agentsPotent 4‐Aminopiperidine Based Antimalarial Agents.
year cv 200520042005
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersChemInformBioorganic & Medicinal Chemistry Letters
kind cv articlearticlearticle
DOI crossref 10.1016/j.bmcl.2004.10.06910.1016/j.bmcl.2004.10.06910.1002/chin.200519159
first author openalex BrinnerBrinnerBrinner

Also recorded as

Citations

OpenAlex
13
Scholar
none
DOI
10.1016/j.bmcl.2004.10.069
OpenAlex
W2106677963

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2005 Preagostic Rh-H Interactions and C-H Bond Functionalization: A Combined Experimental and Theoretical Investigation of Rhodium(I) Phosphinite Complexes Organometallics article journal CV OA GS

CV span

lines 856–858 · CV · published

856203. Lewis, J. C.; Wu, J.; Bergman, R. G.; Ellman, J. A. “Preagostic Rh-H Interactions and C-H Bond857Functionalization: A Combined Experimental and Theoretical Investigation of Rhodium(I)858Phosphinite Complexes” Organometallics 24, 5737-5746 (2005).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C.; Wu, J.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preagostic Rh-H Interactions and C-H Bond Functionalization: A Combined Experimental and Theoretical Investigation of Rhodium(I) Phosphinite ComplexesPreagostic Rh−H Interactions and C−H Bond Functionalization: A Combined Experimental and Theoretical Investigation of Rhodium(I) Phosphinite ComplexesPreagostic Rh− H interactions and C− H bond functionalization: a combined experimental and theoretical investigation of rhodium (I) phosphinite complexes
year cv 200520052005
venue crossref OrganometallicsOrganometallicsOrganometallics
kind cv articlearticleother
DOI crossref 10.1021/om050700i10.1021/om050700i
first author openalex LewisLewisLewis

Citations

OpenAlex
111
Scholar
135
DOI
10.1021/om050700i
OpenAlex
W2019543014

Match decisions

  • doi merged · 1.00 · Run 18
2005 Profiling Serine Protease Substrate Specificity with Solution Phase Fluorogenic Peptide Microarrays PROTEOMICS article journal CV OA GS needs review

CV span

lines 873–875 · CV · published

873208. Ghosalia, D. N.; Salisbury, C. M.; Maly, D. J.; Ellman, J. A.; Diamond, S. L. “Profiling Serine874Protease Substrate Specificity with Solution Phase Fluorogenic Peptide Microarrays” Proteomics 5,8751292-1298 (2005).

Institution fields

Peer reviewed
yes
First author
Ghosalia
Co-authors
Ghosalia, D. N.; Salisbury, C. M.; Maly, D. J.; Ellman, J. A.; Diamond, S. L.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Profiling Serine Protease Substrate Specificity with Solution Phase Fluorogenic Peptide MicroarraysProfiling serine protease substrate specificity with solution phase fluorogenic peptide microarrays
year cv 20052005
venue crossref ProteomicsProteomicsPROTEOMICS
kind cv articleother
DOI crossref 10.1002/pmic.200401011
first author cv GhosaliaGosalia

Citations

OpenAlex
none
Scholar
147
DOI
10.1002/pmic.200401011

Match decisions

  • passthrough_guard not merged · 0.90 · doi_conflict · Run 18 Records describe the same high throughput specificity profiling of proteases using peptide microarrays across slightly different journal manifestations.
  • fingerprint merged · 1.00 · Run 18
2005 Substrate Activity Screening: A Fragment-Based Method for the Rapid Identification of Nonpeptidic Protease Inhibitors Journal of the American Chemical Society article journal CV OA GS

CV span

lines 846–849 · CV · published

846200. Wood, W. J. L.; Patterson, A. W.; Tsuruoka, H.; Jain, R. K.; Ellman, J. A. “Substrate Activity847Screening: A Fragment-Based Method for the Rapid Identification of Nonpeptidic Protease848Inhibitors” J. Am. Chem. Soc. 127, 15521-15527 (2005) [Research Highlight in Nat. Chem. Biol. 1,849359 (2005)].

Institution fields

Peer reviewed
yes
First author
Wood
Co-authors
Wood, W. J. L.; Patterson, A. W.; Tsuruoka, H.; Jain, R. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Substrate Activity Screening: A Fragment-Based Method for the Rapid Identification of Nonpeptidic Protease InhibitorsSubstrate Activity Screening: A Fragment-Based Method for the Rapid Identification of Nonpeptidic Protease InhibitorsSubstrate activity screening: a fragment-based method for the rapid identification of nonpeptidic protease inhibitors
year cv 200520052005
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja054723010.1021/ja0547230
first author openalex WoodWoodWood

Citations

OpenAlex
115
Scholar
146
DOI
10.1021/ja0547230
OpenAlex
W1995946728

Match decisions

  • doi merged · 1.00 · Run 18
2005 Total Synthesis of (+)-Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 860–862 · CV · published

860204. O'Malley, S. J.; Tan, K. L.; Watzke, A.; Bergman, R. G.; Ellman, J. A. “Total Synthesis of (+)-861Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C-H Bond Activation”862J. Am. Chem. Soc. 127, 13496-13497 (2005).

Institution fields

Peer reviewed
yes
First author
O'Malley
Co-authors
O'Malley, S. J.; Tan, K. L.; Watzke, A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Total Synthesis of (+)-Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C-H Bond ActivationTotal Synthesis of (+)-Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C−H Bond ActivationTotal Synthesis of (+)‐Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C—H Bond Activation.Total synthesis of (+)-Lithospermic acid by asymmetric intramolecular alkylation via catalytic C− H bond activation
year cv 2005200520062005
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja052680h10.1021/ja052680h10.1002/chin.200606222
first author openalex O'MalleyO'MalleyO'MalleyO'Malley

Also recorded as

  • W2949140199 (DOI 10.1002/chin.200606222) · same title · 2006 Total Synthesis of (+)‐Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C—H Bond Activation.

Citations

OpenAlex
225
Scholar
251
DOI
10.1021/ja052680h
OpenAlex
W2039560354

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Application of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed Asymmetric Hydrogenation of Olefins The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 933–934 · CV · published

933224. Schenkel, L. B.; Ellman, J. A. “Application of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed934Asymmetric Hydrogenation of Olefins” J. Org. Chem. 69, 1800-1802 (2004).

Institution fields

Peer reviewed
yes
First author
Schenkel
Co-authors
Schenkel, L. B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Application of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed Asymmetric Hydrogenation of OlefinsApplication of P,N‐Sulfinyl Imine Ligands to Iridium‐Catalyzed Asymmetric Hydrogenation of Olefins.Application of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed Asymmetric Hydrogenation of OlefinsApplication of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed Asymmetric Hydrogenation of Olefins
year cv 2004200420042004
venue crossref J. Org. Chem.ChemInformThe Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo035675+10.1002/chin.20043103310.1021/jo035675+
first author openalex SchenkelSchenkelSchenkelSchenkel

Also recorded as

  • W2175526535 (DOI 10.1002/chin.200431033) · same title · 2004 Application of P,N‐Sulfinyl Imine Ligands to Iridium‐Catalyzed Asymmetric Hydrogenation of Olefins.

Citations

OpenAlex
63
Scholar
84
DOI
10.1021/jo035675+
OpenAlex
W2952693093

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Arylation of Heterocycles via Rhodium-Catalyzed C-H Bond Functionalization Organic Letters article journal CV OA GS

CV span

lines 936–937 · CV · published

936225. Lewis, J. C. Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A. “Arylation of Heterocycles via937Rhodium-Catalyzed C-H Bond Functionalization” Org. Lett. 6, 35-38 (2004).

Institution fields

Peer reviewed
yes
First author
Lewis
Co-authors
Lewis, J. C. Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Arylation of Heterocycles via Rhodium-Catalyzed C-H Bond FunctionalizationArylation of Heterocycles via Rhodium-Catalyzed C−H Bond FunctionalizationArylation of Heterocycles via Rhodium‐Catalyzed C—H Bond Functionalization.Arylation of heterocycles via rhodium-catalyzed C− H bond functionalization
year cv 2004200320042004
venue crossref Org. Lett.Organic LettersChemInformOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol035985e10.1021/ol035985e10.1002/chin.200423062
first author openalex LewisLewisLewisLewis

Also recorded as

Citations

OpenAlex
219
Scholar
284
DOI
10.1021/ol035985e
OpenAlex
W2051255862

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Asymmetric -Alkylation of N'-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro- -bisabolene ChemInform article journal CV OA GS

CV span

lines 899–901 · CV · published

899215. Kochi, T.; Ellman, J. A. “Asymmetric -Alkylation of N'-tert-Butanesulfinyl Amidines.900Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro- -bisabolene” J. Am. Chem.901Soc. 126, 15652-15653 (2004).

Institution fields

Peer reviewed
yes
First author
Kochi
Co-authors
Kochi, T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric -Alkylation of N'-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro- -bisaboleneAsymmetric α-Alkylation of N‘-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro-α-bisaboleneAsymmetric α‐Alkylation of N′‐tert‐Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)‐7‐Amino‐7,8‐dihydro‐α‐bisabolene (XIV).Asymmetric α-Alkylation of N‘-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro-α-bisabolene
year cv 2004200420052004
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyChemInform
kind cv articlearticlearticleother
DOI crossref 10.1002/chin.20051703410.1021/ja044753n10.1002/chin.200517034
first author openalex KochiKochiKochiKochi

Also recorded as

  • W1973018553 (DOI 10.1021/ja044753n) · same title · 2004 Asymmetric α-Alkylation of N‘-tert-Butanesulfinyl Amidines. Application to the Total Synthesis of (6R,7S)-7-Amino-7,8-dihydro-α-bisabolene

Citations

OpenAlex
0
Scholar
131
DOI
10.1002/chin.200517034
OpenAlex
W2953203819

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Asymmetric Synthesis of Amines with tert-Butanesulfinamide and Its Application Journal of Synthetic Organic Chemistry, Japan article journal CV OA GS

CV span

lines 923–924 · CV · published

923221. Kochi, T.; Mukade, T. “Asymmetric Synthesis of Amines with tert-Butanesulfinamide and Its924Application” J. Syn. Org. Chem. Jpn. 62, 128-139 (2004).

Institution fields

Peer reviewed
yes
First author
Kochi
Co-authors
Kochi, T.; Mukade, T.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Amines with tert-Butanesulfinamide and Its ApplicationAsymmetric Synthesis of Amines with tert‐Butanesulfinamide and Its ApplicationAsymmetric Synthesis of Amines with tert-Butanesulfinamide and Its Application
year cv 200420042004
venue crossref J. Syn. Org. Chem. Jpn.ChemInformJournal of Synthetic Organic Chemistry JapanJournal of Synthetic Organic Chemistry, Japan
kind cv articlearticlearticle
DOI crossref 10.5059/yukigoseikyokaishi.62.12810.1002/chin.20042823610.5059/yukigoseikyokaishi.62.128
first author openalex KochiKochiKochi

Also recorded as

Citations

OpenAlex
10
Scholar
none
DOI
10.5059/yukigoseikyokaishi.62.128
OpenAlex
W2951873347

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Catalytic Enantioselective Synthesis of Sulfinate Esters Through the Dynamic Resolution of tert-Butanesulfinyl Chloride Journal of the American Chemical Society article journal CV OA GS

CV span

lines 906–908 · CV · published

906217. Evans, J .W.; Fierman, M. B.; Miller, S. J.; Ellman, J. A. “Catalytic Enantioselective Synthesis of907Sulfinate Esters Through the Dynamic Resolution of tert-Butanesulfinyl Chloride” J. Am. Chem.908Soc. 126, 8134-8135 (2004).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, J .W.; Fierman, M. B.; Miller, S. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Enantioselective Synthesis of Sulfinate Esters Through the Dynamic Resolution of tert-Butanesulfinyl ChlorideCatalytic Enantioselective Synthesis of Sulfinate Esters through the Dynamic Resolution of tert -Butanesulfinyl ChlorideCatalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride
year cv 200420042004
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja047845l10.1021/ja047845l
first author openalex EvansEvansEvans

Citations

OpenAlex
121
Scholar
144
DOI
10.1021/ja047845l
OpenAlex
W2079681695

Match decisions

  • doi merged · 1.00 · Run 18
2004 C-H Bond activation by iridium and rhodium complexes: Catalytic hydrogen-deuterium exchange and C-C bond-forming reactions. ACS Symposium Series chapter CV OA GS

CV span

lines 914–918 · CV · published

914219. Klei, S. R.; Tan, K. L.; Golden, J. T.; Yung, C. M.; Thalji, R. K.; Ahrendt, K. A.; Ellman, J. A.;915Tilley, T. D.; Bergman, R. G. “C-H Bond activation by iridium and rhodium complexes: Catalytic916hydrogen-deuterium exchange and C-C bond-forming reactions.” In Activation and917Functionalization of C-H Bonds; Goldberg, K. I.; Goldman, A. S., Ed.; ACS Symposium Series918885; American Chemical Society; Washington, DC, 46-55 (2004).

Institution fields

Peer reviewed
yes
First author
Klei
Co-authors
Klei, S. R.; Tan, K. L.; Golden, J. T.; Yung, C. M.; Thalji, R. K.; Ahrendt, K. A.; Ellman, J. A.; Tilley, T. D.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
American Chemical Society
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv C-H Bond activation by iridium and rhodium complexes: Catalytic hydrogen-deuterium exchange and C-C bond-forming reactions.C—H Bond Activation by Iridium and Rhodium Complexes: Catalytic Hydrogen—Deuterium Exchange and C—C Bond‐Forming ReactionsC—H Bond Activation by Iridium and Rhodium Complexes: Catalytic Hydrogen—Deuterium Exchange and C—C Bond-Forming Reactions
year cv 200420052004
venue crossref Activation and Functionalization of C-H BondsChemInformACS symposium seriesACS Symposium Series
kind cv chapterarticleother
DOI crossref 10.1021/bk-2004-0885.ch00210.1002/chin.20052425110.1021/bk-2004-0885.ch002
first author openalex KleiKleiKlei

Also recorded as

  • W1971003295 (DOI 10.1002/chin.200524251) · same title · 2005 C—H Bond Activation by Iridium and Rhodium Complexes: Catalytic Hydrogen—Deuterium Exchange and C—C Bond‐Forming Reactions

Citations

OpenAlex
3
Scholar
none
DOI
10.1021/bk-2004-0885.ch002
OpenAlex
W2951468843

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Highly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 920–921 · CV · published

920220. Thalji, R. K.; Ellman, J. A.; Bergman, R. G. “Highly Efficient and Enantioselective Cyclization of921Aromatic Imines via Directed C-H Bond Activation” J. Am. Chem. Soc. 126, 7192-7193 (2004).

Institution fields

Peer reviewed
yes
First author
Thalji
Co-authors
Thalji, R. K.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C-H Bond ActivationHighly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C−H Bond ActivationHighly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C—H Bond Activation.Highly efficient and enantioselective cyclization of aromatic imines via directed C− H bond activation
year cv 2004200420042004
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja039498610.1021/ja039498610.1002/chin.200442030
first author openalex ThaljiThaljiThaljiThalji

Also recorded as

  • W2949670009 (DOI 10.1002/chin.200442030) · same title · 2004 Highly Efficient and Enantioselective Cyclization of Aromatic Imines via Directed C—H Bond Activation.

Citations

OpenAlex
292
Scholar
302
DOI
10.1021/ja0394986
OpenAlex
W2107024447

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Highly Stereoselective Addition of Organometallic Reagents to N- tert-Butanesulfinyl Imines Derived from 3- and 4-Substituted Cyclohexanones Organic Letters article journal CV OA GS

CV span

lines 926–928 · CV · published

926222. McMahon, J. P.; Ellman, J. A. “Highly Stereoselective Addition of Organometallic Reagents to N-927tert-Butanesulfinyl Imines Derived from 3- and 4-Substituted Cyclohexanones” Org. Lett. 6, 1645-9281647 (2004).

Institution fields

Peer reviewed
yes
First author
McMahon
Co-authors
McMahon, J. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Highly Stereoselective Addition of Organometallic Reagents to N- tert-Butanesulfinyl Imines Derived from 3- and 4-Substituted CyclohexanonesHighly Stereoselective Addition of Organometallic Reagents to N-tert-Butanesulfinyl Imines Derived from 3- and 4-Substituted CyclohexanonesHighly Stereoselective Addition of Organometallic Reagents to N‐tert‐Butanesulfinyl Imines Derived from 3‐ and 4‐Substituted Cyclohexanones.Highly Stereoselective Addition of Organometallic Reagents to N-tert-Butanesulfinyl Imines Derived from 3- and 4-Substituted Cyclohexanones
year cv 2004200420042004
venue crossref Org. Lett.Organic LettersChemInformOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol049522010.1021/ol049522010.1002/chin.200438078
first author openalex McMahonMcMahonMcMahonMcMahon

Also recorded as

  • W2953000455 (DOI 10.1002/chin.200438078) · same title · 2004 Highly Stereoselective Addition of Organometallic Reagents to N‐tert‐Butanesulfinyl Imines Derived from 3‐ and 4‐Substituted Cyclohexanones.

Citations

OpenAlex
47
Scholar
59
DOI
10.1021/ol0495220
OpenAlex
W1970492343

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2004 Intermolecular Coupling of Alkenes to Heterocycles via C-H Bond Activation The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 903–904 · CV · published

903216. Tan, K. L.; Park, S.; Ellman, J. A.; Bergman, R. G. “Intermolecular Coupling of Alkenes to904Heterocycles via C-H Bond Activation” J. Org. Chem. 69, 7329-7335 (2004).

Institution fields

Peer reviewed
yes
First author
Tan
Co-authors
Tan, K. L.; Park, S.; Ellman, J. A.; Bergman, R. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Intermolecular Coupling of Alkenes to Heterocycles via C-H Bond ActivationIntermolecular Coupling of Alkenes to Heterocycles via C−H Bond ActivationIntermolecular Coupling of Alkenes to Heterocycles via C—H Bond Activation.Intermolecular coupling of alkenes to heterocycles via C− H bond activation
year cv 2004200420052004
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo048666p10.1021/jo048666p10.1002/chin.200508098
first author openalex TanTanTanTan

Also recorded as

Citations

OpenAlex
93
Scholar
123
DOI
10.1021/jo048666p
OpenAlex
W2173939885

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja0281129 for intermolecular coupling of alkenes.
  • doi merged · 1.00 · Run 18
2004 Profiling of protease specificity using combinatorial fluorogenic substrate libraries U.S. Patent No. 6,680,178 other CV OA GS

CV span

lines 1431–1432 · CV · published

143112. Harris, J. L.; Backes, B. J.; Ellman, J. A.; Craig, C. S. “Profiling of protease specificity using1432combinatorial fluorogenic substrate libraries” U.S. (2004) Patent No. 6,680,178.

Institution fields

Peer reviewed
none
First author
Harris
Co-authors
Harris, J. L.; Backes, B. J.; Ellman, J. A.; Craig, C. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Profiling of protease specificity using combinatorial fluorogenic substrate librariesProfiling of protease specificity using combinatorial fluorogenic substrate libraries
year cv 20042004
venue cv U.S. Patent No. 6,680,178US Patent
kind cv otherother
first author cv HarrisHarris

Citations

OpenAlex
none
Scholar
126

Match decisions

  • fingerprint merged · 1.00 · Run 18
2004 Rhodium-Catalyzed Direct C-H Addition of 4,4-Dimethyl-2-oxazoline to Alkenes Organic Letters article journal CV OA GS needs review

CV span

lines 930–931 · CV · published

930223. Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A. “Rhodium-Catalyzed Direct C-H Addition of9314,4-Dimethyl-2-oxazoline to Alkenes” Org. Lett. 6, 1685-1687 (2004).

Institution fields

Peer reviewed
yes
First author
Wiedemann
Co-authors
Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rhodium-Catalyzed Direct C-H Addition of 4,4-Dimethyl-2-oxazoline to AlkenesRhodium‐Catalyzed Direct C—H Addition of 4,4‐Dimethyl‐2‐oxazoline to Alkenes.Rhodium-Catalyzed Direct C−H Addition of 4,4-Dimethyl-2-oxazoline to AlkenesRhodium-catalyzed direct C− H addition of 4, 4-dimethyl-2-oxazoline to alkenes
year cv 2004200420042004
venue crossref Org. Lett.ChemInformOrganic LettersOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol049417q10.1002/chin.20043813010.1021/ol049417q
first author openalex WiedemannWiedemannWiedemannWiedemann

Also recorded as

Citations

OpenAlex
58
Scholar
75
DOI
10.1021/ol049417q
OpenAlex
W2950254443

Match decisions

  • passthrough_guard not merged · 0.80 · low_confidence · Run 18 Group contains two distinct papers by Wiedemann and Ellman on oxazolines and dihydroquinazolines via rhodium catalysis, likely mixed due to related methodology.
  • doi merged · 1.00 · Run 18
2004 Self-Condensation of N-tert-Butanesulfinyl Aldimines: Application to the Asymmetric Synthesis of Biologically Important Amine-Containing Compounds Organic Letters article journal CV OA GS

CV span

lines 910–912 · CV · published

910218. Schenkel, L. B.; Ellman, J. A. “Self-Condensation of N-tert-Butanesulfinyl Aldimines: Application911to the Asymmetric Synthesis of Biologically Important Amine-Containing Compounds” Org. Lett.9126, 3621-3624 (2004).

Institution fields

Peer reviewed
yes
First author
Schenkel
Co-authors
Schenkel, L. B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Self-Condensation of N-tert-Butanesulfinyl Aldimines: Application to the Asymmetric Synthesis of Biologically Important Amine-Containing CompoundsSelf‐Condensation of N‐tert‐Butanesulfinyl Aldimines: Application to the Rapid Asymmetric Synthesis of Biologically Important Amine‐Containing Compounds.Self-Condensation of N-tert-Butanesulfinyl Aldimines: Application to the Rapid Asymmetric Synthesis of Biologically Important Amine-Containing CompoundsSelf-Condensation of N-tert-Butanesulfinyl Aldimines: Application to the Rapid Asymmetric Synthesis of Biologically Important Amine-Containing Compounds
year cv 2004200520042004
venue crossref Org. Lett.ChemInformOrganic LettersOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol048458j10.1002/chin.20050405610.1021/ol048458j
first author openalex SchenkelSchenkelSchenkelSchenkel

Also recorded as

  • W2148850935 (DOI 10.1002/chin.200504056) · same title · 2005 Self‐Condensation of N‐tert‐Butanesulfinyl Aldimines: Application to the Rapid Asymmetric Synthesis of Biologically Important Amine‐Containing Compounds.

Citations

OpenAlex
65
Scholar
90
DOI
10.1021/ol048458j
OpenAlex
W2952939227

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 An Improved Synthesis of tert-Butanesulfinamide Suitable for Large Scale Production Organic Letters article journal CV OA GS

CV span

lines 969–970 · CV · published

969235. Weix, D. J.; Ellman, J. A. “An Improved Synthesis of tert-Butanesulfinamide Suitable for Large970Scale Production” Org. Lett. 5, 1317-1320 (2003).

Institution fields

Peer reviewed
yes
First author
Weix
Co-authors
Weix, D. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv An Improved Synthesis of tert-Butanesulfinamide Suitable for Large Scale ProductionImproved Synthesis of tert-Butanesulfinamide Suitable for Large-Scale ProductionImproved Synthesis of tert‐Butanesulfinamide Suitable for Large‐Scale Production.Improved Synthesis of tert-Butanesulfinamide Suitable for Large-Scale Production
year cv 2003200320032003
venue crossref Org. Lett.Organic LettersChemInformOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol034254b10.1021/ol034254b10.1002/chin.200332055
first author openalex WeixWeixWeixWeix

Also recorded as

Citations

OpenAlex
138
Scholar
217
DOI
10.1021/ol034254b
OpenAlex
W2040273361

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 Applications of tert-Butanesulfinamide in the Asymmetric Synthesis of Amines Pure and Applied Chemistry article journal CV OA GS

CV span

lines 998–999 · CV · published

998243. Ellman, J. A. “Applications of tert-Butanesulfinamide in the Asymmetric Synthesis of Amines”999Pure Appl. Chem. 75, 39-46 (2003).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Applications of tert-Butanesulfinamide in the Asymmetric Synthesis of AminesApplications of tert-butanesulfinamide in the asymmetric synthesis of aminesApplications of tert‐Butanesulfinamide in the Asymmetric Synthesis of AminesApplications of tert-butanesulfinamide in the asymmetric synthesis of amines
year cv 2003200320032003
venue crossref Pure Appl. Chem.Pure and Applied ChemistryChemInformPure and Applied chemistryPure and Applied Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1351/pac20037501003910.1351/pac20037501003910.1002/chin.200338238
first author openalex EllmanEllmanEllmanEllman

Also recorded as

Citations

OpenAlex
249
Scholar
335
DOI
10.1351/pac200375010039
OpenAlex
W2131146694

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 Attenuation of Autoimmune Disease in Fas-Deficient Mice by Treatment with a Cytotoxic Benzodiazepine Arthritis & Rheumatism article CV OA GS

CV span

lines 991–993 · CV · published

991241. Bednarski, J. J.; Warner, R. E.; Rao, T.; Leonetti, F.; Yung, R.; Richardson, B. C.; Johnson, K. J.;992Ellman, J. A. Opipari, A. W.; Glick, G. D. “Attenuation of Autoimmune Disease in Fas-Deficient993Mice by Treatment with a Cytotoxic Benzodiazepine” Arthritis & Rheumatism 48, 757-766 (2003).

Institution fields

Peer reviewed
yes
First author
Bednarski
Co-authors
Bednarski, J. J.; Warner, R. E.; Rao, T.; Leonetti, F.; Yung, R.; Richardson, B. C.; Johnson, K. J.; Ellman, J. A. Opipari, A. W.; Glick, G. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Attenuation of Autoimmune Disease in Fas-Deficient Mice by Treatment with a Cytotoxic BenzodiazepineAttenuation of autoimmune disease in fas‐deficient mice by treatment with a cytotoxic benzodiazepine
year cv 20032003
venue crossref Arthritis & RheumatismArthritis & RheumatismArthritis & Rheumatism
kind cv articleother
DOI crossref 10.1002/art.10968
first author cv BednarskiBednarski

Citations

OpenAlex
none
Scholar
66
DOI
10.1002/art.10968

Match decisions

  • fingerprint merged · 1.00 · Run 18
2003 Catalytic Properties and Inhibition of Proline-Specific Dipeptidyl Peptidases II, IV and VII Biochemical Journal article journal CV OA GS

CV span

lines 972–974 · CV · published

972236. Leiting, B.; Pryor, K. D.; Wu, J. K.; Marsilio, F.; Patel, R. A.; Craik, C. S.; Ellman, J. A.;973Cummings, R. T.; Thornberry, N. “Catalytic Properties and Inhibition of Proline-Specific974Dipeptidyl Peptidases II, IV and VII” Biochem. J. 371, 525-532 (2003).

Institution fields

Peer reviewed
yes
First author
Leiting
Co-authors
Leiting, B.; Pryor, K. D.; Wu, J. K.; Marsilio, F.; Patel, R. A.; Craik, C. S.; Ellman, J. A.; Cummings, R. T.; Thornberry, N.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Properties and Inhibition of Proline-Specific Dipeptidyl Peptidases II, IV and VIICatalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VIICatalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VII
year cv 200320032003
venue crossref Biochem. J.Biochemical JournalBiochemical JournalBiochemical Journal
kind cv articlearticleother
DOI crossref 10.1042/bj2002164310.1042/bj20021643
first author openalex LeitingLeitingLeiting

Citations

OpenAlex
181
Scholar
233
DOI
10.1042/bj20021643
OpenAlex
W2169009504

Match decisions

  • doi merged · 1.00 · Run 18
2003 Crystal Structures of Reversible Ketone-Based Inhibitors of the Cysteine Protease Cruzain Bioorganic & Medicinal Chemistry article journal CV OA GS

CV span

lines 995–996 · CV · published

995242. Huang, L.; Brinen, L. S.; Ellman, J. A. “Crystal Structures of Reversible Ketone-Based Inhibitors996of the Cysteine Protease Cruzain” Bioorg. Med. Chem. 11, 21-29 (2003).

Institution fields

Peer reviewed
yes
First author
Huang
Co-authors
Huang, L.; Brinen, L. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Crystal Structures of Reversible Ketone-Based Inhibitors of the Cysteine Protease CruzainCrystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzainCrystal structures of reversible ketone-based inhibitors of the cysteine protease cruzain
year cv 200320032003
venue crossref Bioorg. Med. Chem.Bioorganic & Medicinal ChemistryBioorganic & medicinal chemistryBioorganic & Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1016/s0968-0896(02)00427-310.1016/s0968-0896(02)00427-3
first author openalex HuangHuangHuang

Citations

OpenAlex
98
Scholar
143
DOI
10.1016/s0968-0896(02)00427-3
OpenAlex
W2095258814

Match decisions

  • doi merged · 1.00 · Run 18
2003 D-Ala-D-Lac Binding is Not Required for the High Activity of Vancomycin Dimers Against Vancomycin Resistant Enterococci Journal of the American Chemical Society article journal CV OA GS

CV span

lines 956–958 · CV · published

956231. Jain, R. K.; Trias, J.; Ellman, J. A. “D-Ala-D-Lac Binding is Not Required for the High Activity of957Vancomycin Dimers Against Vancomycin Resistant Enterococci” J. Am. Chem. Soc. 125, 8740-9588741 (2003).

Institution fields

Peer reviewed
yes
First author
Jain
Co-authors
Jain, R. K.; Trias, J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv D-Ala-D-Lac Binding is Not Required for the High Activity of Vancomycin Dimers Against Vancomycin Resistant Enterococcid -Ala- d -Lac Binding Is Not Required for the High Activity of Vancomycin Dimers against Vancomycin Resistant EnterococciD-Ala-D-Lac binding is not required for the high activity of vancomycin dimers against vancomycin resistant enterococci
year cv 200320032003
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja035976110.1021/ja0359761
first author openalex JainJainJain

Citations

OpenAlex
34
Scholar
54
DOI
10.1021/ja0359761
OpenAlex
W1968324441

Match decisions

  • doi merged · 1.00 · Run 18
2003 Development and Application of a New General Method for the Asymmetric Synthesis of s yn - and a nti -1,3-Amino Alcohols Journal of the American Chemical Society article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Development and Application of a New General Method for the Asymmetric Synthesis of s yn - and a nti -1,3-Amino AlcoholsDevelopment and Application of a New General Method for the Asymmetric Synthesis of s yn-and a nti-1, 3-Amino Alcohols
year openalex 20032003
venue openalex Journal of the American Chemical SocietyJournal of the American Chemical Society
kind openalex articleother
DOI openalex 10.1021/ja0363462
first author openalex KochiKochi

Citations

OpenAlex
181
Scholar
225
DOI
10.1021/ja0363462
OpenAlex
W2057920875

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja0363462 for synthesis of syn- and anti-1,3-amino alcohols.
  • fingerprint merged · 1.00 · Run 18
2003 Development and Application of a New General Method for the Asymmetric Synthesis of syn- and anti-1,3-Amino Alcohols ChemInform article journal CV OA GS needs review

CV span

lines 952–954 · CV · published

952230. Kochi, T.; Tang, T. P.; Ellman, J. A. "Development and Application of a New General Method for953the Asymmetric Synthesis of syn- and anti-1,3-Amino Alcohols" J. Am. Chem. Soc. 125, 11276-95411282 (2003).

Institution fields

Peer reviewed
yes
First author
Kochi
Co-authors
Kochi, T.; Tang, T. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Development and Application of a New General Method for the Asymmetric Synthesis of syn- and anti-1,3-Amino AlcoholsDevelopment and Application of a New General Method for the Asymmetric Synthesis of syn‐ and anti‐1,3‐Amino Alcohols.
year cv 20032003
venue crossref J. Am. Chem. Soc.ChemInformChemInform
kind cv articlearticle
DOI crossref 10.1002/chin.20040106510.1002/chin.200401065
first author openalex KochiKochi

Citations

OpenAlex
3
Scholar
none
DOI
10.1002/chin.200401065
OpenAlex
W2951364450

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja0363462 for synthesis of syn- and anti-1,3-amino alcohols.
  • doi merged · 1.00 · Run 18
2003 Enantioselective Oxidation of Di-tert-Butyl Disulfide with a Vanadium Catalyst: Progress toward Mechanism Elucidation The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1005–1007 · CV · published

1005245. Blum, S. A.; Bergman, R. G.; Ellman, J. A. “Enantioselective Oxidation of Di-tert-Butyl Disulfide1006with a Vanadium Catalyst: Progress toward Mechanism Elucidation” J. Org. Chem. 68, 150-1551007(2003).

Institution fields

Peer reviewed
yes
First author
Blum
Co-authors
Blum, S. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Enantioselective Oxidation of Di-tert-Butyl Disulfide with a Vanadium Catalyst: Progress toward Mechanism ElucidationEnantioselective Oxidation of Di-tert-Butyl Disulfide with a Vanadium Catalyst: Progress toward Mechanism ElucidationEnantioselective Oxidation of Di-tert-Butyl Disulfide with a Vanadium Catalyst: Progress toward Mechanism Elucidation
year cv 200320022003
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo020556010.1021/jo0205560
first author openalex BlumBlumBlum

Citations

OpenAlex
108
Scholar
137
DOI
10.1021/jo0205560
OpenAlex
W2078485670

Match decisions

  • doi merged · 1.00 · Run 18
2003 Identification of Potent and Broad-Spectrum Antibiotics from SAR Studies of a Synthetic Vancomycin Analog Bioorganic & Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 976–978 · CV · published

976237. Ahrendt, K. A.; Olsen, J. A.; Wakao, M.; Trias, J. Ellman, J. A. “Identification of Potent and977Broad-Spectrum Antibiotics from SAR Studies of a Synthetic Vancomycin Analog” Bioorg. Med.978Chem. Lett. 13, 1683-1686 (2003).

Institution fields

Peer reviewed
yes
First author
Ahrendt
Co-authors
Ahrendt, K. A.; Olsen, J. A.; Wakao, M.; Trias, J. Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of Potent and Broad-Spectrum Antibiotics from SAR Studies of a Synthetic Vancomycin AnalogIdentification of potent and broad-Spectrum antibiotics from SAR studies of a synthetic vancomycin analogueIdentification of potent and broad-spectrum antibiotics from SAR studies of a synthetic vancomycin analogue
year cv 200320032003
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic & Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/s0960-894x(03)00243-910.1016/s0960-894x(03)00243-9
first author openalex AhrendtAhrendtAhrendt

Citations

OpenAlex
18
Scholar
35
DOI
10.1016/s0960-894x(03)00243-9
OpenAlex
W2045713908

Match decisions

  • doi merged · 1.00 · Run 18
2003 Microwave Assisted C-H Bond Activation: A Rapid Entry into Functionalized Heterocycles Organic Letters article journal CV OA GS

CV span

lines 963–964 · CV · published

963233. Tan, K. L.; Vasudevan, A.; Bergman, R. G.; Ellman, J. A.; Souers, A. J. “Microwave Assisted C-H964Bond Activation: A Rapid Entry into Functionalized Heterocycles” Org. Lett. 5, 2131-2134 (2003).

Institution fields

Peer reviewed
yes
First author
Tan
Co-authors
Tan, K. L.; Vasudevan, A.; Bergman, R. G.; Ellman, J. A.; Souers, A. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Microwave Assisted C-H Bond Activation: A Rapid Entry into Functionalized HeterocyclesMicrowave-Assisted C−H Bond Activation: A Rapid Entry into Functionalized HeterocyclesMicrowave‐Assisted C—H Bond Activation: A Rapid Entry into Functionalized Heterocycles.Microwave-assisted C− H bond activation: a rapid entry into functionalized heterocycles
year cv 2003200320032003
venue crossref Org. Lett.Organic LettersChemInformOrganic lettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol030050j10.1021/ol030050j10.1002/chin.200340138
first author openalex TanTanTanTan

Also recorded as

Citations

OpenAlex
128
Scholar
155
DOI
10.1021/ol030050j
OpenAlex
W2028846977

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 Novel Sulfinyl Imine Ligands for Asymmetric Catalysis Organic Letters article journal CV OA GS

CV span

lines 988–989 · CV · published

988240. Schenkel, L. B.; Ellman, J. A. “Novel Sulfinyl Imine Ligands for Asymmetric Catalysis” Org. Lett.9895, 545-548 (2003).

Institution fields

Peer reviewed
yes
First author
Schenkel
Co-authors
Schenkel, L. B.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Novel Sulfinyl Imine Ligands for Asymmetric CatalysisNovel Sulfinyl Imine Ligands for Asymmetric CatalysisNovel Sulfinyl Imine Ligands for Asymmetric Catalysis.Novel sulfinyl imine ligands for asymmetric catalysis
year cv 2003200320032003
venue crossref Org. Lett.Organic LettersChemInformOrganic LettersOrganic Letters
kind cv articlearticlearticleother
DOI crossref 10.1021/ol027468m10.1021/ol027468m10.1002/chin.200325034
first author openalex SchenkelSchenkelSchenkelSchenkel

Also recorded as

Citations

OpenAlex
80
Scholar
115
DOI
10.1021/ol027468m
OpenAlex
W2066936401

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 Novel Uncomplexed and Complexed Structures of Plasmepsin II, an Aspartic Protease from Plasmodium falciparum Journal of Molecular Biology article journal CV OA GS

CV span

lines 984–986 · CV · published

984239. Asojo, O. A.; Gulnik. S. V.; Afonina, E.; Yu, B.; Ellman, J. A.; Haque, T. S.; Silva, A. M. “Novel985Uncomplexed and Complexed Structures of Plasmepsin II, an Aspartic Protease from Plasmodium986falciparum” J. Mol. Biol. 327, 173-181 (2003).

Institution fields

Peer reviewed
yes
First author
Asojo
Co-authors
Asojo, O. A.; Gulnik. S. V.; Afonina, E.; Yu, B.; Ellman, J. A.; Haque, T. S.; Silva, A. M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Novel Uncomplexed and Complexed Structures of Plasmepsin II, an Aspartic Protease from Plasmodium falciparumNovel Uncomplexed and Complexed Structures of Plasmepsin II, an Aspartic Protease from Plasmodium falciparumNovel uncomplexed and complexed structures of plasmepsin II, an aspartic protease from Plasmodium falciparum
year cv 200320032003
venue crossref J. Mol. Biol.Journal of Molecular BiologyJournal of molecular biologyJournal of Molecular Biology
kind cv articlearticleother
DOI crossref 10.1016/s0022-2836(03)00036-610.1016/s0022-2836(03)00036-6
first author openalex AsojoAsojoAsojo

Citations

OpenAlex
152
Scholar
187
DOI
10.1016/s0022-2836(03)00036-6
OpenAlex
W2048833096

Match decisions

  • doi merged · 1.00 · Run 18
2003 Parallel Solution-Phase Asymmetric Synthesis of -Branched Amines Journal of Combinatorial Chemistry article journal CV OA GS

CV span

lines 960–961 · CV · published

960232. Mukade, T.; Dragoli, D. R.; Ellman, J. A. “Parallel Solution-Phase Asymmetric Synthesis of -961Branched Amines” J. Comb. Chem. 5, 590-596 (2003).

Institution fields

Peer reviewed
yes
First author
Mukade
Co-authors
Mukade, T.; Dragoli, D. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Parallel Solution-Phase Asymmetric Synthesis of -Branched AminesParallel Solution‐Phase Asymmetric Synthesis of α‐Branched Amines.Parallel Solution-Phase Asymmetric Synthesis of α-Branched AminesParallel solution-phase asymmetric synthesis of α-branched amines
year cv 2003200420032003
venue crossref J. Comb. Chem.ChemInformJournal of Combinatorial ChemistryJournal of Combinatorial ChemistryJournal of Combinatorial Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/cc030016w10.1002/chin.20040606710.1021/cc030016w
first author openalex MukadeMukadeMukadeMukade

Also recorded as

Citations

OpenAlex
50
Scholar
66
DOI
10.1021/cc030016w
OpenAlex
W2952908127

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 (RS)‐(+)‐2‐Methyl‐2‐propanesulfinamide [tert‐Butanesulfinamide] Organic Syntheses article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title scholar (RS)‐(+)‐2‐Methyl‐2‐propanesulfinamide [tert‐Butanesulfinamide]
year scholar 2003
venue scholar Organic Syntheses
kind scholar other
first author scholar Weix

Citations

OpenAlex
none
Scholar
74

Match decisions

No decision recorded; a single record.

2003 Stereoselective Synthesis of 1,2-Disubstituted -Amino Alcohols by Nucleophilic Addition to N-tert-Butanesulfinyl aldimines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 939–940 · CV · published

939226. Evans, J. W.; Ellman, J. A. “Stereoselective Synthesis of 1,2-Disubstituted -Amino Alcohols by940Nucleophilic Addition to N-tert-Butanesulfinyl aldimines” J. Org. Chem. 68, 9948-9957 (2003).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, J. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Stereoselective Synthesis of 1,2-Disubstituted -Amino Alcohols by Nucleophilic Addition to N-tert-Butanesulfinyl aldiminesStereoselective Synthesis of 1,2‐Disubstituted β‐Amino Alcohols by Nucleophilic Addition to N‐tert‐Butanesulfinyl α‐Alkoxyaldimines.Stereoselective Synthesis of 1,2-Disubstituted β-Amino Alcohols by Nucleophilic Addition to N-tert-Butanesulfinyl α-AlkoxyaldiminesStereoselective Synthesis of 1,2-Disubstituted β-Amino Alcohols by Nucleophilic Addition to N-tert-Butanesulfinyl α-Alkoxyaldimines
year cv 2003200420032003
venue crossref J. Org. Chem.ChemInformThe Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo035224p10.1002/chin.20041907010.1021/jo035224p
first author openalex EvansEvansEvansEvans

Also recorded as

  • W2105791110 (DOI 10.1002/chin.200419070) · platform twin · 2004 Stereoselective Synthesis of 1,2‐Disubstituted β‐Amino Alcohols by Nucleophilic Addition to N‐tert‐Butanesulfinyl α‐Alkoxyaldimines.

Citations

OpenAlex
71
Scholar
96
DOI
10.1021/jo035224p
OpenAlex
W2949475498

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2003 Structure Activity Studies of a Novel Cytotoxic Benzodiazepine Bioorganic & Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 948–950 · CV · published

948229. Boitano, A.; Leonetii, F.; Emal, C.; Ellman, J. A.; Roush, W. R.; Opipari, A. W.; Glick, G. D.949“Structure Activity Studies of a Novel Cytotoxic Benzodiazepine” Bioorg. Med. Chem. Lett. 13,9503327-3330 (2003).

Institution fields

Peer reviewed
yes
First author
Boitano
Co-authors
Boitano, A.; Leonetii, F.; Emal, C.; Ellman, J. A.; Roush, W. R.; Opipari, A. W.; Glick, G. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Structure Activity Studies of a Novel Cytotoxic BenzodiazepineStructure activity studies of a novel cytotoxic benzodiazepineStructure Activity Studies of a Novel Cytotoxic Benzodiazepine.Structure activity studies of a novel cytotoxic benzodiazepine
year cv 2003200320032003
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersChemInformBioorganic & medicinal chemistry lettersBioorganic & Medicinal Chemistry Letters
kind cv articlearticlearticleother
DOI crossref 10.1016/s0960-894x(03)00683-810.1016/s0960-894x(03)00683-810.1002/chin.200401144
first author openalex BoitanoBoitanoBoitanoBoitano

Also recorded as

Citations

OpenAlex
16
Scholar
42
DOI
10.1016/s0960-894x(03)00683-8
OpenAlex
W2136181908

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 Synthesis and Characterization of the First Potent Inhibitor of Yapsin 1. Implications for the Study of Yapsin-Like Enzymes Journal of Biological Chemistry article journal CV OA GS

CV span

lines 980–982 · CV · published

980238. Cawley, N. X.; Chino, M.; Maldonado, A.; Rodriguez, Y. M.; Loh, Y. P.; Ellman, J. A. “Synthesis981and Characterization of the First Potent Inhibitor of Yapsin 1. Implications for the Study of Yapsin-982Like Enzymes” J. Biol. Chem. 278, 5523-5530 (2003).

Institution fields

Peer reviewed
yes
First author
Cawley
Co-authors
Cawley, N. X.; Chino, M.; Maldonado, A.; Rodriguez, Y. M.; Loh, Y. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Characterization of the First Potent Inhibitor of Yapsin 1. Implications for the Study of Yapsin-Like EnzymesSynthesis and Characterization of the First Potent Inhibitor of Yapsin 1
year cv 20032003
venue crossref J. Biol. Chem.Journal of Biological ChemistryJournal of Biological Chemistry
kind cv articlearticle
DOI crossref 10.1074/jbc.m20723020010.1074/jbc.m207230200
first author openalex CawleyCawley

Citations

OpenAlex
12
Scholar
none
DOI
10.1074/jbc.m207230200
OpenAlex
W2076368251

Match decisions

  • doi merged · 1.00 · Run 18
2003 Synthesis of a Diverse Library of Mechanism-Based Cysteine Protease Inhibitors Journal of Combinatorial Chemistry article journal CV OA GS

CV span

lines 942–943 · CV · published

942227. Wood, W.; Huang, L.; Ellman, J. A. “Synthesis of a Diverse Library of Mechanism-Based Cysteine943Protease Inhibitors” J. Comb. Chem. 5, 869-880 (2003).

Institution fields

Peer reviewed
yes
First author
Wood
Co-authors
Wood, W.; Huang, L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of a Diverse Library of Mechanism-Based Cysteine Protease InhibitorsSynthesis of a Diverse Library of Mechanism-Based Cysteine Protease InhibitorsSynthesis of a diverse library of mechanism-based cysteine protease inhibitors
year cv 200320032003
venue crossref J. Comb. Chem.Journal of Combinatorial ChemistryJournal of Combinatorial ChemistryJournal of Combinatorial Chemistry
kind cv articlearticleother
DOI crossref 10.1021/cc034008r10.1021/cc034008r
first author openalex WoodWoodWood

Citations

OpenAlex
23
Scholar
40
DOI
10.1021/cc034008r
OpenAlex
W1991090669

Match decisions

  • doi merged · 1.00 · Run 18
2003 Synthesis of a Tricyclic Mescaline Analog by Catalytic C-H Bond Activation Organic Letters article journal CV OA GS

CV span

lines 966–967 · CV · published

966234. Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A. “Synthesis of a Tricyclic Mescaline Analog by967Catalytic C-H Bond Activation” Org. Lett. 5, 1301-1303 (2003).

Institution fields

Peer reviewed
yes
First author
Ahrendt
Co-authors
Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of a Tricyclic Mescaline Analog by Catalytic C-H Bond ActivationSynthesis of a Tricyclic Mescaline Analogue by Catalytic C−H Bond ActivationSynthesis of a Tricyclic Mescaline Analogue by Catalytic C− H Bond Activation
year cv 200320032003
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol034228d10.1021/ol034228d
first author openalex AhrendtAhrendtAhrendt

Citations

OpenAlex
99
Scholar
129
DOI
10.1021/ol034228d
OpenAlex
W2043147672

Match decisions

  • doi merged · 1.00 · Run 18
2003 The Preparation and Utility of Bis(sulfinyl)imidoamidine Ligands for the Copper-Catalyzed Diels Alder Reaction The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1001–1003 · CV · published

1001244. Owens, T. D.; Souers, A. J.; Ellman, J. A. “The Preparation and Utility of1002Bis(sulfinyl)imidoamidine Ligands for the Copper-Catalyzed Diels Alder Reaction” J. Org. Chem.100368, 3-10 (2003).

Institution fields

Peer reviewed
yes
First author
Owens
Co-authors
Owens, T. D.; Souers, A. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Preparation and Utility of Bis(sulfinyl)imidoamidine Ligands for the Copper-Catalyzed Diels Alder ReactionThe Preparation and Utility of Bis(sulfinyl)imidoamidine Ligands for the Copper‐Catalyzed Diels—Alder Reaction.The Preparation and Utility of Bis(sulfinyl)imidoamidine Ligands for the Copper-Catalyzed Diels−Alder ReactionThe Preparation and Utility of Bis (sulfinyl) imidoamidine Ligands for the Copper-Catalyzed Diels− Alder Reaction
year cv 2003200320022003
venue crossref J. Org. Chem.ChemInformThe Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo020524c10.1002/chin.20032102610.1021/jo020524c
first author openalex OwensOwensOwensOwens

Also recorded as

  • W2100386446 (DOI 10.1002/chin.200321026) · same title · 2003 The Preparation and Utility of Bis(sulfinyl)imidoamidine Ligands for the Copper‐Catalyzed Diels—Alder Reaction.

Citations

OpenAlex
86
Scholar
102
DOI
10.1021/jo020524c
OpenAlex
W2949486180

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2003 The Proapoptotic Benzodiazepine BZ-423 Affects the Growth and Survival of Malignant B Cells J. Cancer Res. article CV OA GS

CV span

lines 945–946 · CV · published

945228. Boitano, A.; Ellman, J. A.; Glick, G. D.; Opipari, A. W. “The Proapoptotic Benzodiazepine BZ-423946Affects the Growth and Survival of Malignant B Cells” J. Cancer Res. 63, 6870-6876 (2003).

Institution fields

Peer reviewed
yes
First author
Boitano
Co-authors
Boitano, A.; Ellman, J. A.; Glick, G. D.; Opipari, A. W.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv The Proapoptotic Benzodiazepine BZ-423 Affects the Growth and Survival of Malignant B CellsThe proapoptotic benzodiazepine Bz-423 affects the growth and survival of malignant B cells.The proapoptotic benzodiazepine Bz-423 affects the growth and survival of malignant B cells
year cv 200320032003
venue cv J. Cancer Res.PubMedCancer research
kind cv articlearticleother
first author openalex BoitanoBoitanoBoitano

Citations

OpenAlex
31
Scholar
53
OpenAlex
W1540852269

Match decisions

  • fingerprint merged · 1.00 · Run 18
2002 Altered Substrate Specificity of Drug-Resistant Human Immunodeficiency Virus Type 1 Protease Journal of Virology article journal CV OA GS

CV span

lines 1064–1066 · CV · published

1064262. Dauber, D. S.; Ziermann, R. Parkin, N.; Maly, D. J.; Mahrus, S.; Harris, J. L.; Ellman, J. A.;1065Petropoulos, C.; Craik, C. S. “Altered Substrate Specificity of Drug-Resistant Human1066Immunodeficiency Virus Type 1 Protease” J. Virol. 76, 1359-1368 (2002).

Institution fields

Peer reviewed
yes
First author
Dauber
Co-authors
Dauber, D. S.; Ziermann, R. Parkin, N.; Maly, D. J.; Mahrus, S.; Harris, J. L.; Ellman, J. A.; Petropoulos, C.; Craik, C. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Altered Substrate Specificity of Drug-Resistant Human Immunodeficiency Virus Type 1 ProteaseAltered substrate specificity of drug-resistant human immunodeficiency virus type 1 protease
year cv 20022002
venue crossref J. Virol.Journal of virologyJournal of Virology
kind cv articleother
DOI crossref 10.1128/jvi.76.3.1359-1368.2002
first author cv DauberDauber

Citations

OpenAlex
none
Scholar
85
DOI
10.1128/jvi.76.3.1359-1368.2002

Match decisions

  • fingerprint merged · 1.00 · Run 18
2002 Asymmetric Synthesis of -Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions to tert-Butanesulfinyl Imines The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 1015–1017 · CV · published

1015248. Tang, T. P.; Ellman, J. A. “Asymmetric Synthesis of -Amino Acid Derivatives Incorporating a1016Broad Range of Substitution Patterns by Enolate Additions to tert-Butanesulfinyl Imines” J. Org.1017Chem. 67, 7819-7832 (2002).

Institution fields

Peer reviewed
yes
First author
Tang
Co-authors
Tang, T. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of -Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions to tert-Butanesulfinyl IminesAsymmetric Synthesis of β-Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions totert-Butanesulfinyl IminesAsymmetric Synthesis of β‐Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions to tert‐Butanesulfinyl Imines.Asymmetric Synthesis of β-Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions to tert-Butanesulfinyl Imines
year cv 2002200220032002
venue crossref J. Org. Chem.The Journal of Organic ChemistryChemInformThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticlearticleother
DOI crossref 10.1021/jo025957u10.1021/jo025957u10.1002/chin.200314188
first author openalex TangTangTangTang

Also recorded as

  • W2953284355 (DOI 10.1002/chin.200314188) · same title · 2003 Asymmetric Synthesis of β‐Amino Acid Derivatives Incorporating a Broad Range of Substitution Patterns by Enolate Additions to tert‐Butanesulfinyl Imines.

Citations

OpenAlex
177
Scholar
233
DOI
10.1021/jo025957u
OpenAlex
W2144429758

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo061160h for propargylamines synthesis.
  • doi merged · 1.00 · Run 18
2002 Asymmetric Synthesis of syn- and anti-1,3-Amino Alcohols ChemInform article journal CV OA GS needs review

CV span

lines 1040–1041 · CV · published

1040255. Kochi, T.; Tang, T. P.; Ellman, J. A. “Asymmetric Synthesis of syn- and anti-1,3-Amino Alcohols”1041J. Am. Chem. Soc. 124, 6518-6519 (2002).

Institution fields

Peer reviewed
yes
First author
Kochi
Co-authors
Kochi, T.; Tang, T. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of syn- and anti-1,3-Amino AlcoholsAsymmetric Synthesis of syn- and anti-1,3-Amino AlcoholsAsymmetric Synthesis of syn‐ and anti‐1,3‐Amino Alcohols.Asymmetric Synthesis of s yn-and a nti-1, 3-Amino Alcohols
year cv 2002200220022002
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyChemInform
kind cv articlearticlearticleother
DOI crossref 10.1002/chin.20024203310.1021/ja026292g10.1002/chin.200242033
first author openalex KochiKochiKochiKochi

Also recorded as

Citations

OpenAlex
0
Scholar
175
DOI
10.1002/chin.200242033
OpenAlex
W2950089764

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja026292g for asymmetric synthesis of syn- and anti-1,3-amino alcohols.
  • doi merged · 1.00 · Run 18
2002 Benzodiazepine-Induced Superoxidce Signals B Cell Apoptosis: Mechanistic Insight and Potential Therapeutic Utility Journal of Clinical Investigation article journal CV OA GS

CV span

lines 1019–1022 · CV · published

1019249. Blatt, N. B.; Bednarski, J. J.; Warner, R. E.; Leonetti, F.; Johnson, K. M.; Boitano, A.; Yung, R.;1020Richardson, B. C.; Johnson, K. J.; Ellman, J. A. Opipari, A. W.; Glick, G. D. “Benzodiazepine-1021Induced Superoxidce Signals B Cell Apoptosis: Mechanistic Insight and Potential Therapeutic1022Utility” J. Clin. Invest. 110, 1123-1132 (2002).

Institution fields

Peer reviewed
yes
First author
Blatt
Co-authors
Blatt, N. B.; Bednarski, J. J.; Warner, R. E.; Leonetti, F.; Johnson, K. M.; Boitano, A.; Yung, R.; Richardson, B. C.; Johnson, K. J.; Ellman, J. A. Opipari, A. W.; Glick, G. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Benzodiazepine-Induced Superoxidce Signals B Cell Apoptosis: Mechanistic Insight and Potential Therapeutic UtilityBenzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utilityBenzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utilityBenzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utilityBenzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utility
year cv 20022002200220022002
venue crossref J. Clin. Invest.Journal of Clinical InvestigationJournal of Clinical InvestigationJournal of Clinical InvestigationThe Journal of clinical investigationJournal of Clinical Investigation
kind cv articlearticlearticlearticleother
DOI crossref 10.1172/jci021602910.1172/jci1602910.1172/jci021602910.1172/jci200216029
first author openalex BlattBlattBlattBlattBlatt

Also recorded as

  • W2117994321 (DOI 10.1172/jci16029) · platform twin · 2002 Benzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utility
  • W4255595865 (DOI 10.1172/jci200216029) · platform twin · 2002 Benzodiazepine-induced superoxide signalsB cell apoptosis: mechanistic insight and potential therapeutic utility

Citations

OpenAlex
59
Scholar
120
DOI
10.1172/jci0216029
OpenAlex
W4243151643

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: platform_twin
2002 Combinatorial Strategies for Targeting Protein Families. Application to the Proteases ChemBioChem article journal CV OA GS needs review

CV span

lines 1057–1058 · CV · published

1057260. Maly, D. J.; Huang, L.; Ellman, J. A. “Combinatorial Strategies for Targeting Protein Families.1058Application to the Proteases” ChemBioChem 3, 16-37 (2002).

Institution fields

Peer reviewed
yes
First author
Maly
Co-authors
Maly, D. J.; Huang, L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Combinatorial Strategies for Targeting Protein Families. Application to the ProteasesCombinatorial Strategies for Targeting Protein Families: Application to the ProteasesCombinatorial strategies for targeting protein families: application to the proteases
year cv 200220022002
venue crossref ChemBioChemChemBioChemChemBioChem
kind cv articlearticleother
DOI crossref 10.1002/1439-7633(20020104)3:1<16::aid-cbic16>3.0.co;2-z10.1002/1439-7633(20020104)3:1<16::aid-cbic16>3.0.co;2-z
first author openalex MalyMalyMaly

Citations

OpenAlex
64
Scholar
117
DOI
10.1002/1439-7633(20020104)3:1<16::aid-cbic16>3.0.co;2-z
OpenAlex
W2054518327

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1002/1439-7633(20020104)3:1<16::aid-cbic16>3.0.co;2-z for combinatorial strategies targeting protein families.
  • doi merged · 1.00 · Run 18
2002 Design and Synthesis of Novel Inhibitors of Gelatinase B Bioorganic &amp; Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 1043–1044 · CV · published

1043256. Wang, X.; Choe, Y.; Craik, C. S.; Ellman, J. A. “Design and Synthesis of Novel Inhibitors of1044Gelatinase B” Bioorg. Med. Chem. Lett. 12, 2201-2204 (2002).

Institution fields

Peer reviewed
yes
First author
Wang
Co-authors
Wang, X.; Choe, Y.; Craik, C. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design and Synthesis of Novel Inhibitors of Gelatinase BDesign and synthesis of novel inhibitors of gelatinase BDesign and synthesis of novel inhibitors of gelatinase B
year cv 200220022002
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic &amp; Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/s0960-894x(02)00365-710.1016/s0960-894x(02)00365-7
first author openalex WangWangWang

Citations

OpenAlex
21
Scholar
40
DOI
10.1016/s0960-894x(02)00365-7
OpenAlex
W2017040371

Match decisions

  • doi merged · 1.00 · Run 18
2002 Efficient Method to prepare hydroxyethylamine-based aspartyl protease inhibitors with diverse P1 side chains Tetrahedron article journal CV OA GS

CV span

lines 1034–1035 · CV · published

1034253. Chino, M.; Wakao, M.; Ellman, J. A. “Efficient Method to prepare hydroxyethylamine-based1035aspartyl protease inhibitors with diverse P1 side chains” Tetrahedron 58, 6305-6310 (2002).

Institution fields

Peer reviewed
yes
First author
Chino
Co-authors
Chino, M.; Wakao, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Efficient Method to prepare hydroxyethylamine-based aspartyl protease inhibitors with diverse P1 side chainsEfficient method to prepare hydroxyethylamine-based aspartyl protease inhibitors with diverse P1 side chains
year cv 20022002
venue crossref TetrahedronTetrahedron
kind cv articlearticle
DOI crossref 10.1016/s0040-4020(02)00629-410.1016/s0040-4020(02)00629-4
first author openalex ChinoChino

Citations

OpenAlex
11
Scholar
none
DOI
10.1016/s0040-4020(02)00629-4
OpenAlex
W2020283497

Match decisions

  • doi merged · 1.00 · Run 18
2002 Expedient Solid-Phase Synthesis of Fluorogenic Protease Substrates Using the 7-Amino-4-Carbamoylmethylcoumarin (ACC) Fluorophore The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1053–1055 · CV · published

1053259. Maly, D. J.; Leonetti, F.; Backes, B. J.; Dauber, D. S.; Harris, J. L.; Craik, C. S.; Ellman, J. A.1054“Expedient Solid-Phase Synthesis of Fluorogenic Protease Substrates Using the 7-Amino-4-1055Carbamoylmethylcoumarin (ACC) Fluorophore” J. Org. Chem. 67, 910-915 (2002).

Institution fields

Peer reviewed
yes
First author
Maly
Co-authors
Maly, D. J.; Leonetti, F.; Backes, B. J.; Dauber, D. S.; Harris, J. L.; Craik, C. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Expedient Solid-Phase Synthesis of Fluorogenic Protease Substrates Using the 7-Amino-4-Carbamoylmethylcoumarin (ACC) FluorophoreExpedient Solid-Phase Synthesis of Fluorogenic Protease Substrates Using the 7-Amino-4-carbamoylmethylcoumarin (ACC) FluorophoreExpedient solid-phase synthesis of fluorogenic protease substrates using the 7-amino-4-carbamoylmethylcoumarin (ACC) fluorophore
year cv 200220022002
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of organic chemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo016140o10.1021/jo016140o
first author openalex MalyMalyMaly

Citations

OpenAlex
141
Scholar
201
DOI
10.1021/jo016140o
OpenAlex
W2003113488

Match decisions

  • doi merged · 1.00 · Run 18
2002 General Solid-Phase Procedure to Prepare Novel Cyclic Ketone Inhibitors of the Cysteine Protease Cruzain Bioorganic &amp; Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 1027–1028 · CV · published

1027251. Huang, L.; Ellman, J. A. “General Solid-Phase Procedure to Prepare Novel Cyclic Ketone1028Inhibitors of the Cysteine Protease Cruzain” Bioorg. Med. Chem. Lett. 12, 2993-2996 (2002).

Institution fields

Peer reviewed
yes
First author
Huang
Co-authors
Huang, L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General Solid-Phase Procedure to Prepare Novel Cyclic Ketone Inhibitors of the Cysteine Protease CruzainGeneral solid-phase method to prepare novel cyclic ketone inhibitors of the cysteine protease cruzain
year cv 20022002
venue crossref Bioorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic &amp; Medicinal Chemistry Letters
kind cv articlearticle
DOI crossref 10.1016/s0960-894x(02)00619-410.1016/s0960-894x(02)00619-4
first author openalex HuangHuang

Citations

OpenAlex
16
Scholar
none
DOI
10.1016/s0960-894x(02)00619-4
OpenAlex
W2038628469

Match decisions

  • doi merged · 1.00 · Run 18
2002 Identification of Potent and Selective Mechanism-Based Inhibitors of the Cysteine Protease Cruzain Using Solid-Phase Parallel Synthesis Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 1060–1062 · CV · published

1060261. Huang, L.; Lee, A.; Ellman, J. A. “Identification of Potent and Selective Mechanism-Based1061Inhibitors of the Cysteine Protease Cruzain Using Solid-Phase Parallel Synthesis” J. Med. Chem.106245, 676-684 (2002).

Institution fields

Peer reviewed
yes
First author
Huang
Co-authors
Huang, L.; Lee, A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of Potent and Selective Mechanism-Based Inhibitors of the Cysteine Protease Cruzain Using Solid-Phase Parallel SynthesisIdentification of Potent and Selective Mechanism-Based Inhibitors of the Cysteine Protease Cruzain Using Solid-Phase Parallel SynthesisIdentification of potent and selective mechanism-based inhibitors of the cysteine protease cruzain using solid-phase parallel synthesis
year cv 200220012002
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm010333m10.1021/jm010333m
first author openalex HuangHuangHuang

Citations

OpenAlex
58
Scholar
92
DOI
10.1021/jm010333m
OpenAlex
W2078046457

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jm010333m for identification of cruzain inhibitors.
2002 Interference with Heme Binding to Histidine-Rich Protein-2 As an Antimalarial Strategy Chemistry &amp; Biology article journal CV OA GS

CV span

lines 1030–1032 · CV · published

1030252. Choi, C. Y. H.; Schneider, E. L.; Kim, J. M.; Gluzman, I. Y.; Goldberg, D. E.; Ellman, J. A.;1031Marletta, A. “Interference with Heme Binding to Histidine-Rich Protein-2 As an Antimalarial1032Strategy” Chem. Biol. 9, 881-889 (2002).

Institution fields

Peer reviewed
yes
First author
Choi
Co-authors
Choi, C. Y. H.; Schneider, E. L.; Kim, J. M.; Gluzman, I. Y.; Goldberg, D. E.; Ellman, J. A.; Marletta, A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Interference with Heme Binding to Histidine-Rich Protein-2 As an Antimalarial StrategyInterference with Heme Binding to Histidine-Rich Protein-2 as an Antimalarial StrategyInterference with heme binding to histidine-rich protein-2 as an antimalarial strategy
year cv 200220022002
venue crossref Chem. Biol.Chemistry & BiologyChemistry & biologyChemistry &amp; Biology
kind cv articlearticleother
DOI crossref 10.1016/s1074-5521(02)00183-710.1016/s1074-5521(02)00183-7
first author openalex ChoiChoiChoi

Citations

OpenAlex
25
Scholar
33
DOI
10.1016/s1074-5521(02)00183-7
OpenAlex
W1999439874

Match decisions

  • doi merged · 1.00 · Run 18
2002 Intermediacy of an N-Heterocyclic Carbene in the Catalytic C-H Activation of Benzimidazole Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1046–1047 · CV · published

1046257. Tan, K. L.; Bergman, R. G.; Ellman, J. A. “Intermediacy of an N-Heterocyclic Carbene in the1047Catalytic C-H Activation of Benzimidazole” J. Am. Chem. Soc. 124, 3202-3203 (2002).

Institution fields

Peer reviewed
yes
First author
Tan
Co-authors
Tan, K. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Intermediacy of an N-Heterocyclic Carbene in the Catalytic C-H Activation of BenzimidazoleIntermediacy of an N-Heterocyclic Carbene Complex in the Catalytic C−H Activation of a Substituted BenzimidazoleIntermediacy of an N-heterocyclic carbene complex in the catalytic C− H activation of a substituted benzimidazole
year cv 200220022002
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja017351d10.1021/ja017351d
first author openalex TanTanTan

Citations

OpenAlex
188
Scholar
243
DOI
10.1021/ja017351d
OpenAlex
W1974464721

Match decisions

  • doi merged · 1.00 · Run 18
2002 Intermolecular Coupling of Alkenes to Heterocycles via Rhodium-Catalyzed C-H Bond Activation Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1024–1025 · CV · published

1024250. Tan, K. L.; Bergman, R. G.; Ellman, J. A. “Intermolecular Coupling of Alkenes to Heterocycles via1025Rhodium-Catalyzed C-H Bond Activation” J. Am. Chem. Soc. 124, 13964-13965 (2002).

Institution fields

Peer reviewed
yes
First author
Tan
Co-authors
Tan, K. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Intermolecular Coupling of Alkenes to Heterocycles via Rhodium-Catalyzed C-H Bond ActivationIntermolecular Coupling of Isomerizable Alkenes to Heterocycles via Rhodium-Catalyzed C−H Bond ActivationIntermolecular Coupling of Isomerizable Alkenes to Heterocycles via Rhodium‐Catalyzed C—H Bond Activation.Intermolecular coupling of isomerizable alkenes to heterocycles via rhodium-catalyzed C− H bond activation
year cv 2002200220032002
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja028112910.1021/ja028112910.1002/chin.200315109
first author openalex TanTanTanTan

Also recorded as

  • W2952329541 (DOI 10.1002/chin.200315109) · platform twin · 2003 Intermolecular Coupling of Isomerizable Alkenes to Heterocycles via Rhodium‐Catalyzed C—H Bond Activation.

Citations

OpenAlex
155
Scholar
183
DOI
10.1021/ja0281129
OpenAlex
W2050400197

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja0281129 for intermolecular coupling of alkenes.
  • doi merged · 1.00 · Run 18
2002 Novel and Potent Anti-Malarial Agents Bioorganic &amp; Medicinal Chemistry article journal CV OA GS

CV span

lines 1037–1038 · CV · published

1037254. Brinner, K. M.; Kim, J. M.; Habashita, H.; Gluzman, I. Y.; Goldberg, D. E.; Ellman, J. A. “Novel1038and Potent Anti-Malarial Agents” Bioorg. Med. Chem. 10, 3649-3661 (2002).

Institution fields

Peer reviewed
yes
First author
Brinner
Co-authors
Brinner, K. M.; Kim, J. M.; Habashita, H.; Gluzman, I. Y.; Goldberg, D. E.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Novel and Potent Anti-Malarial AgentsNovel and Potent Anti-malarial AgentsNovel and potent anti-malarial agents
year cv 200220022002
venue crossref Bioorg. Med. Chem.Bioorganic & Medicinal ChemistryBioorganic & medicinal chemistryBioorganic &amp; Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1016/s0968-0896(02)00207-910.1016/s0968-0896(02)00207-9
first author openalex BrinnerBrinnerBrinner

Citations

OpenAlex
22
Scholar
38
DOI
10.1016/s0968-0896(02)00207-9
OpenAlex
W2074494791

Match decisions

  • doi merged · 1.00 · Run 18
2002 N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines Accounts of Chemical Research article journal CV OA GS

CV span

lines 1012–1013 · CV · published

1012247. Ellman, J. A.; Owens, T. D.; Tang, T. P. “N-tert-Butanesulfinyl Imines: Versatile Intermediates for1013the Asymmetric Synthesis of Amines” Acc. Chem. Res. 35, 984-995 (2002).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J. A.; Owens, T. D.; Tang, T. P.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of AminesN-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of AminesN‐tert‐Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of AminesN-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines
year cv 2002200220032002
venue crossref Acc. Chem. Res.Accounts of Chemical ResearchChemInformAccounts of chemical researchAccounts of Chemical Research
kind cv articlearticlearticleother
DOI crossref 10.1021/ar020066u10.1021/ar020066u10.1002/chin.200307222
first author openalex EllmanEllmanEllmanEllman

Also recorded as

Citations

OpenAlex
830
Scholar
1093
DOI
10.1021/ar020066u
OpenAlex
W2168679251

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2002 Peptide Microarrays for the Determination of Substrate Specificity Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1009–1010 · CV · published

1009246. Salisbury, C. M.; Maly, D. J.; Ellman, J. A. “Peptide Microarrays for the Determination of1010Substrate Specificity” J. Am. Chem. Soc. 124, 14868-14870 (2002).

Institution fields

Peer reviewed
yes
First author
Salisbury
Co-authors
Salisbury, C. M.; Maly, D. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Peptide Microarrays for the Determination of Substrate SpecificityPeptide Microarrays for the Determination of Protease Substrate SpecificityPeptide microarrays for the determination of protease substrate specificity
year cv 200220022002
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja027477q10.1021/ja027477q
first author openalex SalisburySalisburySalisbury

Citations

OpenAlex
252
Scholar
342
DOI
10.1021/ja027477q
OpenAlex
W2083015173

Match decisions

  • doi merged · 1.00 · Run 18
2002 Tyrosylprotein Sulfotransferase Inhibitors Generated by Combinatorial Target-Guided ligand Assembly Bioorganic &amp; Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 1049–1051 · CV · published

1049258. Kehoe, J. W.; Maly, D. J.; Verdugo, D. E.; Armstrong, J. I.; Cook, B. N.; Ouyang, Y.-B.; Moore, K.1050L.; Ellman, J. A.; Bertozzi, C. R. “Tyrosylprotein Sulfotransferase Inhibitors Generated by1051Combinatorial Target-Guided ligand Assembly” Bioorg. Med. Chem. Lett 12, 329-332 (2002).

Institution fields

Peer reviewed
yes
First author
Kehoe
Co-authors
Kehoe, J. W.; Maly, D. J.; Verdugo, D. E.; Armstrong, J. I.; Cook, B. N.; Ouyang, Y.-B.; Moore, K. L.; Ellman, J. A.; Bertozzi, C. R.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Tyrosylprotein Sulfotransferase Inhibitors Generated by Combinatorial Target-Guided ligand AssemblyTyrosylprotein sulfotransferase inhibitors generated by combinatorial target-Guided ligand assemblyTyrosylprotein sulfotransferase inhibitors generated by combinatorial target-guided ligand assembly
year cv 200220022002
venue crossref Bioorg. Med. Chem. LettBioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic &amp; Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/s0960-894x(01)00744-210.1016/s0960-894x(01)00744-2
first author openalex KehoeKehoeKehoe

Citations

OpenAlex
46
Scholar
58
DOI
10.1016/s0960-894x(01)00744-2
OpenAlex
W2070527088

Match decisions

  • doi merged · 1.00 · Run 18
2001 A Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C–H Activation Angewandte Chemie International Edition article CV OA GS

CV span

lines 1102–1104 · CV · published

1102273. Szewczyk, J. W.; Zuckermann, R. L.; Bergman, R. G.; Ellman, J. A. “A Mass Spectrometric1103Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C–H1104Activation” Angew. Chem. Int. Ed. 40, 216-219 (2001).

Institution fields

Peer reviewed
yes
First author
Szewczyk
Co-authors
Szewczyk, J. W.; Zuckermann, R. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C–H ActivationA Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C-H Activation This work was supported by the Director, Office of Energy Research, Office of Basic Energy Sciences, Chemical Sciences Division, U.S. Department of Energy, under contract No. DE-AC03-76SF00098. We are grateful to the National Institutes of Health for support (GM-50353) and for a Postdoctoral Fellowship to J.W.S.A Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C−H ActivationA Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C−H ActivationA Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C−H ActivationA mass spectrometric labeling strategy for high‐throughput reaction evaluation and optimization: exploring C− H activation
year cv 200120012001200120012001
venue crossref Angew. Chem. Int. Ed.PubMedAngewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International EditionAngewandte ChemieAngewandte Chemie International Edition
kind cv articlearticlearticlearticlearticleother
DOI crossref 10.1002/1521-3773(20010105)40:1<216::aid-anie216>3.0.co;2-k10.1002/1521-3773(20010105)40:1<216::aid-anie216>3.0.co;2-k10.1002/1521-3773(20010105)40:1<216::aid-anie216>3.3.co;2-b10.1002/1521-3757(20010105)113:1<222::aid-ange222>3.0.co;2-e10.1002/1521-3773(20010105)40:1<216::aid-anie216>3.0.co;2-k
first author openalex SzewczykSzewczykSzewczykSzewczykSzewczykSzewczyk

Also recorded as

Citations

OpenAlex
59
Scholar
80
DOI
10.1002/1521-3773(20010105)40:1<216::aid-anie216>3.0.co;2-k
OpenAlex
W2171551301

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2001 Annulation of Alkenyl-Substituted Heterocycles via Rhodium-Catalyzed Intramolecular C-H Activated Coupling Reactions Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1091–1093 · CV · published

1091270. Tan, K. L.; Bergman, R. G.; Ellman, J. A. “Annulation of Alkenyl-Substituted Heterocycles via1092Rhodium-Catalyzed Intramolecular C-H Activated Coupling Reactions” J. Am. Chem. Soc. 123,10932685-2686 (2001).

Institution fields

Peer reviewed
yes
First author
Tan
Co-authors
Tan, K. L.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Annulation of Alkenyl-Substituted Heterocycles via Rhodium-Catalyzed Intramolecular C-H Activated Coupling ReactionsAnnulation of Alkenyl-Substituted Heterocycles via Rhodium-Catalyzed Intramolecular C−H Activated Coupling ReactionsAnnulation of Alkenyl‐Substituted Heterocycles via Rhodium‐Catalyzed Intramolecular C—H Activated Coupling Reactions.Annulation of alkenyl-substituted heterocycles via rhodium-catalyzed intramolecular C− H activated coupling reactions
year cv 2001200120012001
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyChemInformJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticlearticleother
DOI crossref 10.1021/ja005873810.1021/ja005873810.1002/chin.200129130
first author openalex TanTanTanTan

Also recorded as

  • W2949117594 (DOI 10.1002/chin.200129130) · same title · 2001 Annulation of Alkenyl‐Substituted Heterocycles via Rhodium‐Catalyzed Intramolecular C—H Activated Coupling Reactions.

Citations

OpenAlex
173
Scholar
226
DOI
10.1021/ja0058738
OpenAlex
W1989127118

Match decisions

  • classified merged · 1.00 · Run 18 resolved by the OpenAlex classification: same_title
2001 Annulation of Aromatic Imines via Directed C-H Activation with Wilkinson’s Catalyst Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1074–1075 · CV · published

1074265. Thalji, R.; Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A. “Annulation of Aromatic Imines via1075Directed C-H Activation with Wilkinson’s Catalyst” J. Am. Chem. Soc. 123, 9692-9693 (2001).

Institution fields

Peer reviewed
yes
First author
Thalji
Co-authors
Thalji, R.; Ahrendt, K. A.; Bergman, R. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Annulation of Aromatic Imines via Directed C-H Activation with Wilkinson’s CatalystAnnulation of Aromatic Imines via Directed C−H Activation with Wilkinson's CatalystAnnulation of aromatic imines via directed C− H activation with wilkinson's catalyst
year cv 200120012001
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja016642j10.1021/ja016642j
first author openalex ThaljiThaljiThalji

Citations

OpenAlex
225
Scholar
259
DOI
10.1021/ja016642j
OpenAlex
W1986600892

Match decisions

  • doi merged · 1.00 · Run 18
2001 Asymmetric Synthesis of 1,2-Amino Alcohols Using tert-Butanesulfinyl Aldimines and Ketimines The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1071–1072 · CV · published

1071264. Tang, T. P.; Volkman, S. K.; Ellman, J. A. “Asymmetric Synthesis of 1,2-Amino Alcohols Using1072tert-Butanesulfinyl Aldimines and Ketimines” J. Org. Chem. 66, 8772-8778 (2001).

Institution fields

Peer reviewed
yes
First author
Tang
Co-authors
Tang, T. P.; Volkman, S. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of 1,2-Amino Alcohols Using tert-Butanesulfinyl Aldimines and KetiminesAsymmetric Synthesis of Protected 1,2-Amino Alcohols Using tert-Butanesulfinyl Aldimines and KetiminesAsymmetric Synthesis of Protected 1,2-Amino Alcohols Using tert-Butanesulfinyl Aldimines and Ketimines
year cv 200120012001
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo015686810.1021/jo0156868
first author openalex TangTangTang

Citations

OpenAlex
109
Scholar
170
DOI
10.1021/jo0156868
OpenAlex
W2041108021

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jo0156868 for asymmetric synthesis of 1,2-amino alcohols.
2001 Asymmetric Synthesis of Pre-Protected ,-Disubstituted Amino Acids from tert-Butanesulfinyl Ketimines Tetrahedron Letters article journal CV OA GS

CV span

lines 1095–1096 · CV · published

1095271. Borg, G.; Chino, M.; Ellman, J. A. “Asymmetric Synthesis of Pre-Protected ,-Disubstituted1096Amino Acids from tert-Butanesulfinyl Ketimines” Tetrahedron Lett. 42, 1433-1436 (2001).

Institution fields

Peer reviewed
yes
First author
Borg
Co-authors
Borg, G.; Chino, M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Pre-Protected ,-Disubstituted Amino Acids from tert-Butanesulfinyl KetiminesAsymmetric synthesis of pre-protected α,α-disubstituted amino acids from tert-butanesulfinyl ketiminesAsymmetric synthesis of pre-protected α, α-disubstituted amino acids from tert-butanesulfinyl ketimines
year cv 200120012001
venue crossref Tetrahedron Lett.Tetrahedron LettersTetrahedron LettersTetrahedron Letters
kind cv articlearticleother
DOI crossref 10.1016/s0040-4039(00)02300-510.1016/s0040-4039(00)02300-5
first author openalex BorgBorgBorg

Citations

OpenAlex
77
Scholar
104
DOI
10.1016/s0040-4039(00)02300-5
OpenAlex
W1985616540

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jo0156868 for asymmetric synthesis of 1,2-amino alcohols.
2001 Definition of the Extended Substrate Specificity Determinants for -Tryptases I and II Journal of Biological Chemistry article journal CV OA GS

CV span

lines 1087–1089 · CV · published

1087269. Harris, J. L.; Niles, A.; Burdick, K.; Maffitt, M.; Backes, B. J.; Ellman, J. A.; Kuntz, I.; Haak-1088Frendscho, M.; Craik, C. S. “Definition of the Extended Substrate Specificity Determinants for -1089Tryptases I and II” J. Biol. Chem. 276, 34941-34947 (2001).

Institution fields

Peer reviewed
yes
First author
Harris
Co-authors
Harris, J. L.; Niles, A.; Burdick, K.; Maffitt, M.; Backes, B. J.; Ellman, J. A.; Kuntz, I.; Haak-Frendscho, M.; Craik, C. S.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Definition of the Extended Substrate Specificity Determinants for -Tryptases I and IIDefinition of the Extended Substrate Specificity Determinants for β-Tryptases I and IIDefinition of the extended substrate specificity determinants for β-tryptases I and II
year cv 200120012001
venue crossref J. Biol. Chem.Journal of Biological ChemistryJournal of Biological ChemistryJournal of Biological Chemistry
kind cv articlearticleother
DOI crossref 10.1074/jbc.m10299720010.1074/jbc.m102997200
first author openalex HarrisHarrisHarris

Citations

OpenAlex
59
Scholar
88
DOI
10.1074/jbc.m102997200
OpenAlex
W1998331667

Match decisions

  • doi merged · 1.00 · Run 18
2001 Design, Synthesis, and Utility of Support-Bound tert-Butanesulfinamide Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1084–1085 · CV · published

1084268. Dragoli, D. R.; Burdett, M. T.; Ellman, J. A. “Design, Synthesis, and Utility of Support-Bound tert-1085Butanesulfinamide” J. Am. Chem. Soc. 123, 10127-10128 (2001).

Institution fields

Peer reviewed
yes
First author
Dragoli
Co-authors
Dragoli, D. R.; Burdett, M. T.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design, Synthesis, and Utility of Support-Bound tert-ButanesulfinamideDesign, Synthesis, and Utility of a Support-Bound tert-ButanesulfinamideDesign, synthesis, and utility of a support-bound tert-butanesulfinamide
year cv 200120012001
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja016349j10.1021/ja016349j
first author openalex DragoliDragoliDragoli

Citations

OpenAlex
69
Scholar
107
DOI
10.1021/ja016349j
OpenAlex
W2013601794

Match decisions

  • doi merged · 1.00 · Run 18
2001 Parallel Solution-Phase Synthesis of Mechanism-Based Cysteine Protease Inhibitors Organic Letters article journal CV OA GS

CV span

lines 1068–1069 · CV · published

1068263. Lee. A.; Ellman, J. A. “Parallel Solution-Phase Synthesis of Mechanism-Based Cysteine Protease1069Inhibitors” Org. Lett. 3, 3707-3709 (2001).

Institution fields

Peer reviewed
yes
First author
Lee
Co-authors
Lee. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Parallel Solution-Phase Synthesis of Mechanism-Based Cysteine Protease InhibitorsParallel Solution-Phase Synthesis of Mechanism-Based Cysteine Protease InhibitorsParallel solution-phase synthesis of mechanism-based cysteine protease inhibitors
year cv 200120012001
venue crossref Org. Lett.Organic LettersOrganic LettersOrganic Letters
kind cv articlearticleother
DOI crossref 10.1021/ol016649610.1021/ol0166496
first author openalex LeeLeeLee

Citations

OpenAlex
23
Scholar
37
DOI
10.1021/ol0166496
OpenAlex
W1971773865

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jm010333m for identification of cruzain inhibitors.
2001 Preparation of 4-amino-1-benzylpiperidines as antimalarials PCT Int. Appl. other CV OA GS

CV span

lines 1503–1504 · CV · published

150314. Kim, J. M.; Ellman, J. A.; Goldberg, D. “Preparation of 4-amino-1-benzylpiperidines as1504antimalarials” PCT Int. Appl. (2001), WO 0114331 A2 2001030.

Institution fields

Peer reviewed
none
First author
Kim
Co-authors
Kim, J. M.; Ellman, J. A.; Goldberg, D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of 4-amino-1-benzylpiperidines as antimalarials
year cv 2001
venue cv PCT Int. Appl.
kind cv other
first author cv Kim

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2001 Synthesis and Crystal Structure of a Unique and Homochiral N,S-Bonded N,N-Bis(-tert-Butanesulfinyl)amidinate Rhodium(I) Complex Inorganic Chemistry article journal CV OA GS

CV span

lines 1080–1082 · CV · published

1080267. Souers, A. J.; Owens, T. D.; Oliver, A. G.; Hollander, F. J.; Ellman, J. A. “Synthesis and Crystal1081Structure of a Unique and Homochiral N,S-Bonded N,N-Bis(-tert-Butanesulfinyl)amidinate1082Rhodium(I) Complex” Inorg. Chem. 40, 5299-5301 (2001).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Owens, T. D.; Oliver, A. G.; Hollander, F. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Crystal Structure of a Unique and Homochiral N,S-Bonded N,N-Bis(-tert-Butanesulfinyl)amidinate Rhodium(I) ComplexSynthesis and Crystal Structure of a Unique and Homochiral N,S-Bonded N,N‘-Bis(tert-butanesulfinyl)amidinate Rhodium(I) Complex
year cv 20012001
venue crossref Inorg. Chem.Inorganic ChemistryInorganic Chemistry
kind cv articlearticle
DOI crossref 10.1021/ic010420510.1021/ic0104205
first author openalex SouersSouers

Citations

OpenAlex
20
Scholar
none
DOI
10.1021/ic0104205
OpenAlex
W2018174140

Match decisions

  • doi merged · 1.00 · Run 18
2001 Synthesis, Utility, and Structure of Novel Bis(sulfinyl)imidoamidine Ligands for Asymmetric Lewis Acid Catalysis Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1098–1100 · CV · published

1098272. Owens, T. D.; Hollander, F. J.; Oliver, A. G.; Ellman, J. A. “Synthesis, Utility, and Structure of1099Novel Bis(sulfinyl)imidoamidine Ligands for Asymmetric Lewis Acid Catalysis” J. Am. Chem.1100Soc. 123, 1539-1540 (2001).

Institution fields

Peer reviewed
yes
First author
Owens
Co-authors
Owens, T. D.; Hollander, F. J.; Oliver, A. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis, Utility, and Structure of Novel Bis(sulfinyl)imidoamidine Ligands for Asymmetric Lewis Acid CatalysisSynthesis, Utility, and Structure of Novel Bis(sulfinyl)imidoamidine Ligands for Asymmetric Lewis Acid CatalysisSynthesis, utility, and structure of novel bis (sulfinyl) imidoamidine ligands for asymmetric Lewis acid catalysis
year cv 200120012001
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja005635c10.1021/ja005635c
first author openalex OwensOwensOwens

Citations

OpenAlex
119
Scholar
144
DOI
10.1021/ja005635c
OpenAlex
W2953250122

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja005635c for bis(sulfinyl)imidoamidine ligands.
  • doi merged · 1.00 · Run 18
2001 -Turn Mimetic Library Synthesis: Scaffolds and Applications Tetrahedron article journal CV OA GS needs review

CV span

lines 1077–1078 · CV · published

1077266. Souers, A. J.; Ellman, J. A. “-Turn Mimetic Library Synthesis: Scaffolds and Applications”1078Tetrahedron 57, 7431-7448 (2001).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv -Turn Mimetic Library Synthesis: Scaffolds and Applicationsβ-Turn mimetic library synthesis: scaffolds and applicationsβ-Turn mimetic library synthesis: scaffolds and applications
year cv 200120012001
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/s0040-4020(01)00680-910.1016/s0040-4020(01)00680-9
first author openalex SouersSouersSouers

Citations

OpenAlex
158
Scholar
195
DOI
10.1016/s0040-4020(01)00680-9
OpenAlex
W2021967959

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/s0040-4020(01)00680-9 for beta-turn mimetic library synthesis.
  • doi merged · 1.00 · Run 18
2000 Asymmetric Synthesis of a C-3 Substituted Pipecolic Acid The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 1130–1131 · CV · published

1130280. Souers, A. J.; Ellman, J. A. “Asymmetric Synthesis of a C-3 Substituted Pipecolic Acid” J. Org.1131Chem. 65, 1222-1224 (2000).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of a C-3 Substituted Pipecolic AcidAsymmetric Synthesis of a C-3 Substituted Pipecolic AcidAsymmetric synthesis of a C-3 substituted pipecolic acid
year cv 200020002000
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo991293l10.1021/jo991293l
first author openalex SouersSouersSouers

Citations

OpenAlex
34
Scholar
32
DOI
10.1021/jo991293l
OpenAlex
W2950253111

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo991293l for asymmetric synthesis of pipecolic acid.
  • doi merged · 1.00 · Run 18
2000 Combinatorial Libraries for Drug Development Stimulating Concepts in Chemistry chapter CV OA GS

CV span

lines 1114–1116 · CV · published

1114276. Lee, A.; Szewczyk, J. W.; Ellman, J. A. “Combinatorial Libraries for Drug Development” in1115“Stimulating Concepts in Chemistry” Vogtle, F.; Stoddart, J. F.; Shibasaki, M. Ed.; Wiley-VCH,1116Weinheim, 2000, pp. 65-78.

Institution fields

Peer reviewed
none
First author
Lee
Co-authors
Lee, A.; Szewczyk, J. W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
Wiley-VCH
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Combinatorial Libraries for Drug DevelopmentCombinatorial Libraries for Drug Development
year cv 20002000
venue crossref Stimulating Concepts in Chemistry
kind cv chapterother
DOI crossref 10.1002/3527605746.ch510.1002/3527605746.ch5
first author openalex LeeLee

Citations

OpenAlex
1
Scholar
none
DOI
10.1002/3527605746.ch5
OpenAlex
W2004433873

Match decisions

  • doi merged · 1.00 · Run 18
2000 Combinatorial Methods to Engineer Small Molecules for Functional Genomics The Role of Natural Products in Drug Discovery chapter CV OA GS

CV span

lines 1118–1120 · CV · published

1118277. Ellman, J. A. “Combinatorial Methods to Engineer Small Molecules for Functional Genomics”, in1119Ernst Schering Research Foundation Workshop 32, “The Role of Natural Products in Drug1120Discovery” Mulzer, J. and Bohlmann, R. Ed.; Springer, New York, 2000, pp. 183-204.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
Springer
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Methods to Engineer Small Molecules for Functional GenomicsCombinatorial Methods to Engineer Small Molecules for Functional Genomics
year cv 20002000
venue crossref Ernst Schering Research Foundation Workshop 32, “The Role of Natural Products in Drug Discovery”The Role of Natural Products in Drug Discovery
kind cv chapterchapter
DOI crossref 10.1007/978-3-662-04042-3_610.1007/978-3-662-04042-3_6
first author openalex EllmanEllman

Citations

OpenAlex
3
Scholar
none
DOI
10.1007/978-3-662-04042-3_6
OpenAlex
W197946017

Match decisions

  • doi merged · 1.00 · Run 18
2000 Combinatorial Target-Guided Ligand Assembly. Identification of Potent, Sub-type Selective c-Src Inhibitors Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 1126–1128 · CV · published

1126279. Maly, D. J.; Choong, I. C.; Ellman, J. A. “Combinatorial Target-Guided Ligand Assembly.1127Identification of Potent, Sub-type Selective c-Src Inhibitors” Proc. Natl. Acad. Sci. 97, 2419-24241128(2000).

Institution fields

Peer reviewed
yes
First author
Maly
Co-authors
Maly, D. J.; Choong, I. C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Target-Guided Ligand Assembly. Identification of Potent, Sub-type Selective c-Src InhibitorsCombinatorial target-guided ligand assembly: Identification of potent subtype-selective c-Src inhibitorsCombinatorial target-guided ligand assembly: identification of potent subtype-selective c-Src inhibitors
year cv 200020002000
venue crossref Proc. Natl. Acad. Sci.Proceedings of the National Academy of SciencesProceedings of the National Academy of SciencesProceedings of the National Academy of Sciences
kind cv articlearticleother
DOI crossref 10.1073/pnas.97.6.241910.1073/pnas.97.6.2419
first author openalex MalyMalyMaly

Citations

OpenAlex
190
Scholar
303
DOI
10.1073/pnas.97.6.2419
OpenAlex
W2047222471

Match decisions

  • doi merged · 1.00 · Run 18
2000 Inhibitors of protein tyrosine kinases U.S. Patent No. 6,100,254 other CV OA GS

CV span

lines 1443–1444 · CV · published

144316. Budde, R, J. A.; Ellman, J. A.; Levin, V. A.; Gallick, G. E.; Newman, R. A.; “Inhibitors of protein1444tyrosine kinases” U.S. (2000), Patent No. 6,100,254.

Institution fields

Peer reviewed
none
First author
Budde
Co-authors
Budde, R, J. A.; Ellman, J. A.; Levin, V. A.; Gallick, G. E.; Newman, R. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Inhibitors of protein tyrosine kinasesInhibitors of protein tyrosine kinases
year cv 20002000
venue cv U.S. Patent No. 6,100,254US Patent
kind cv otherother
first author cv BuddeBudde

Citations

OpenAlex
none
Scholar
90

Match decisions

  • fingerprint merged · 1.00 · Run 18
2000 Methods for treating neurodegenerative disorders using aspartyl protease inhibitors PCT Int. Appl. reprint 2006 Methods for Treating Neurodegenerative Disorders using Aspartyl Protease Inhibitors other CV OA GS

CV span

lines 1506–1508 · CV · published

150615. Ellman, J. A.; Lynch, G.; Kuntz, I. D.; Bi, X.; Lee, C. E.; Skillman, A. G.; Haque, T. “Methods for1507treating neurodegenerative disorders using aspartyl protease inhibitors” PCT Int. Appl. (2000), WO15080056335 A1 20000928.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J. A.; Lynch, G.; Kuntz, I. D.; Bi, X.; Lee, C. E.; Skillman, A. G.; Haque, T.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Methods for treating neurodegenerative disorders using aspartyl protease inhibitors
year cv 2000
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2000 Nanomolar, Non-Peptide Inhibitors of Cathepsin D U.S. Patent No. 6,150,416 other CV OA GS

CV span

lines 1440–1441 · CV · published

144015. Kick, E. K.; Ellman, J. A.; Kuntz, I. D.; Lee, C. E.; Liu, G.; Roe, D. C.; Skillman, A. G.1441“Nanomolar, Non-Peptide Inhibitors of Cathepsin D” U.S. (2000), Patent No. 6,150,416.

Institution fields

Peer reviewed
none
First author
Kick
Co-authors
Kick, E. K.; Ellman, J. A.; Kuntz, I. D.; Lee, C. E.; Liu, G.; Roe, D. C.; Skillman, A. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Nanomolar, Non-Peptide Inhibitors of Cathepsin D
year cv 2000
venue cv U.S. Patent No. 6,150,416
kind cv other
first author cv Kick

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

2000 Novel Cathepsin D Inhibitors Block the Formation of Hyperphosphorylated Tau Fragments in Hippocampus Journal of Neurochemistry article journal CV OA GS

CV span

lines 1122–1124 · CV · published

1122278. Bi, X.; Lin, B. Haque, T.; Lee, C. E.; Skillman, A. G.; Kuntz, I. D.; Ellman, J. A.; Lynch, G.1123“Novel Cathepsin D Inhibitors Block the Formation of Hyperphosphorylated Tau Fragments in1124Hippocampus” J. Neurochem. 74, 1469-1477 (2000).

Institution fields

Peer reviewed
yes
First author
Bi
Co-authors
Bi, X.; Lin, B. Haque, T.; Lee, C. E.; Skillman, A. G.; Kuntz, I. D.; Ellman, J. A.; Lynch, G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Novel Cathepsin D Inhibitors Block the Formation of Hyperphosphorylated Tau Fragments in HippocampusNovel Cathepsin D Inhibitors Block the Formation of Hyperphosphorylated Tau Fragments in HippocampusNovel cathepsin D inhibitors block the formation of hyperphosphorylated tau fragments in hippocampus
year cv 200020002000
venue crossref J. Neurochem.Journal of NeurochemistryJournal of neurochemistryJournal of Neurochemistry
kind cv articlearticleother
DOI crossref 10.1046/j.1471-4159.2000.0741469.x10.1046/j.1471-4159.2000.0741469.x
first author openalex BiBiBi

Citations

OpenAlex
70
Scholar
101
DOI
10.1046/j.1471-4159.2000.0741469.x
OpenAlex
W2005069707

Match decisions

  • doi merged · 1.00 · Run 18
2000 Optimization of a Somatostatin Mimetic via Constrained amino acid and Backbone Incorporation Bioorganic &amp; Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 1110–1112 · CV · published

1110275. Souers, A. J.; Rosenquist, A.; Jarvie, E. M.; Ladlow, M.; Fenuik, W.; Ellman, J. A. “Optimization1111of a Somatostatin Mimetic via Constrained amino acid and Backbone Incorporation” Biorg. Med.1112Chem. Lett. 10, 2731-2733 (2000).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Rosenquist, A.; Jarvie, E. M.; Ladlow, M.; Fenuik, W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Optimization of a Somatostatin Mimetic via Constrained amino acid and Backbone IncorporationOptimization of a somatostatin mimetic via constrained amino acid and backbone incorporation
year cv 20002000
venue crossref Biorg. Med. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic &amp; Medicinal Chemistry Letters
kind cv articlearticle
DOI crossref 10.1016/s0960-894x(00)00552-710.1016/s0960-894x(00)00552-7
first author openalex SouersSouers

Citations

OpenAlex
17
Scholar
none
DOI
10.1016/s0960-894x(00)00552-7
OpenAlex
W2072494222

Match decisions

  • doi merged · 1.00 · Run 18
2000 Rapid and General Profiling of Protease Specificity by Using Combinatorial Fluorogenic Substrate Libraries Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 1106–1108 · CV · published

1106274. Backes, B. J.; Harris, J. L.; Leonetti, F.; Ellman, J. A.; Craik, C. “Rapid and General Profiling of1107Protease Specificity by Using Combinatorial Fluorogenic Substrate Libraries” Proc. Natl. Acad.1108Sci. 97, 7754-7759 (2000).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Harris, J. L.; Leonetti, F.; Ellman, J. A.; Craik, C.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Rapid and General Profiling of Protease Specificity by Using Combinatorial Fluorogenic Substrate LibrariesRapid and general profiling of protease specificity by using combinatorial fluorogenic substrate librariesRapid and general profiling of protease specificity by using combinatorial fluorogenic substrate libraries
year cv 200020002000
venue crossref Proc. Natl. Acad. Sci.Proceedings of the National Academy of SciencesProceedings of the National Academy of SciencesProceedings of the National Academy of Sciences
kind cv articlearticleother
DOI crossref 10.1073/pnas.14013269710.1073/pnas.140132697
first author openalex BackesHarrisHarris

Citations

OpenAlex
546
Scholar
740
DOI
10.1073/pnas.140132697
OpenAlex
W2103700658

Match decisions

  • doi merged · 1.00 · Run 18
2000 Strategy to Prepare Positional Scanning Libraries of Fluorogenic Peptide Substrates that Incorporate Diverse P1 Substituents: Facile and Accurate Specificity Determination of Thrombin and Plasmin Nat. Biotechnology article CV OA GS

CV span

lines 1133–1136 · CV · published

1133281. Backes, B. J.; Harris, J. L.; Leonetti, F.; Craik, C.; Ellman, J. A. “Strategy to Prepare Positional1134Scanning Libraries of Fluorogenic Peptide Substrates that Incorporate Diverse P1 Substituents:1135Facile and Accurate Specificity Determination of Thrombin and Plasmin” Nat. Biotechnology 18,1136187-194 (2000).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Harris, J. L.; Leonetti, F.; Craik, C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Strategy to Prepare Positional Scanning Libraries of Fluorogenic Peptide Substrates that Incorporate Diverse P1 Substituents: Facile and Accurate Specificity Determination of Thrombin and Plasmin
year cv 2000
venue cv Nat. Biotechnology
kind cv article
first author cv Backes

Citations

OpenAlex
none
Scholar
none

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1038/72642 for positional-scanning libraries of fluorogenic peptide substrates.
2000 Synthesis of positional-scanning libraries of fluorogenic peptide substrates to define the extended substrate specificity of plasmin and thrombin Nature Biotechnology article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Synthesis of positional-scanning libraries of fluorogenic peptide substrates to define the extended substrate specificity of plasmin and thrombinSynthesis of positional-scanning libraries of fluorogenic peptide substrates to define the extended substrate specificity of plasmin and thrombin
year openalex 20002000
venue openalex Nature BiotechnologyNature biotechnology
kind openalex articleother
DOI openalex 10.1038/72642
first author openalex BackesBackes

Citations

OpenAlex
248
Scholar
355
DOI
10.1038/72642
OpenAlex
W2050756511

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1038/72642 for positional-scanning libraries of fluorogenic peptide substrates.
2000 Targeted Libraries Proceedings of the 16th American Peptide Symposium conference paper CV OA GS

CV span

lines 1148–1150 · CV · published

1148285. Huang, L.; Lee, A.; Ellman, J. A. “Targeted Libraries”, in Proceedings of the 16th American1149Peptide Symposium, Fields, G. B.; Tam, J. P.; and Kerwin, J. F. Ed.; Kluwer Academic Publishers,1150Inc.: Boston, 2000, pp. 161-163.

Institution fields

Peer reviewed
none
First author
Huang
Co-authors
Huang, L.; Lee, A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
Kluwer Academic Publishers, Inc.
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Targeted Libraries
year cv 2000
venue cv Proceedings of the 16th American Peptide Symposium
kind cv conference_paper
first author cv Huang

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1999 An Alkanesulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1183–1184 · CV · published

1183294. Backes, B. J.; Ellman, J. A. “An Alkanesulfonamide “Safety-Catch” Linker for Solid-Phase1184Synthesis” J. Org. Chem. 64, 2322-2330 (1999).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv An Alkanesulfonamide “Safety-Catch” Linker for Solid-Phase SynthesisAn Alkanesulfonamide “Safety-Catch” Linker for Solid-Phase SynthesisAn alkanesulfonamide “safety-catch” linker for solid-phase synthesis
year cv 199919991999
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo981990y10.1021/jo981990y
first author openalex BackesBackesBackes

Citations

OpenAlex
203
Scholar
338
DOI
10.1021/jo981990y
OpenAlex
W2002480858

Match decisions

  • doi merged · 1.00 · Run 18
1999 Asymmetric Synthesis of Chiral Amines by Highly Diastereoselective 1,2-Additions of Organometallic Reagents to N-tert-Butanesulfinyl Imines Tetrahedron article journal CV OA GS needs review

CV span

lines 1175–1177 · CV · published

1175292. Cogan, D. A.; Liu, G.; Ellman, J. “Asymmetric Synthesis of Chiral Amines by Highly1176Diastereoselective 1,2-Additions of Organometallic Reagents to N-tert-Butanesulfinyl Imines”1177Tetrahedron 55, 8883-8904 (1999).

Institution fields

Peer reviewed
yes
First author
Cogan
Co-authors
Cogan, D. A.; Liu, G.; Ellman, J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Asymmetric Synthesis of Chiral Amines by Highly Diastereoselective 1,2-Additions of Organometallic Reagents to N-tert-Butanesulfinyl IminesAsymmetric synthesis of chiral amines by highly diastereoselective 1,2-additions of organometallic reagents to N-tert-butanesulfinyl iminesAsymmetric synthesis of chiral amines by highly diastereoselective 1, 2-additions of organometallic reagents to N-tert-butanesulfinyl imines
year cv 199919991999
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/s0040-4020(99)00451-210.1016/s0040-4020(99)00451-2
first author openalex CoganCoganCogan

Citations

OpenAlex
334
Scholar
491
DOI
10.1016/s0040-4020(99)00451-2
OpenAlex
W1997595536

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/s0040-4020(99)00451-2 for asymmetric synthesis of chiral amines.
  • doi merged · 1.00 · Run 18
1999 Benzodiazepine Compounds as Inhibitors of the Src Protein Tyrosine Kinase: Screening of a Combinatorial Library of 1,4-Benzodiazepines Archives of Biochemistry and Biophysics article journal CV OA GS

CV span

lines 1156–1159 · CV · published

1156287. Ramdas, L.; Bunin, B. A.; Plunkett, M. J.; Sun, G.; Ellman, J. A.; Gallick, G.; Budde, R. J. A.1157“Benzodiazepine Compounds as Inhibitors of the Src Protein Tyrosine Kinase: Screening of a1158Combinatorial Library of 1,4-Benzodiazepines” Archives of Biochem. And Biophys. 368, 394-4001159(1999).

Institution fields

Peer reviewed
yes
First author
Ramdas
Co-authors
Ramdas, L.; Bunin, B. A.; Plunkett, M. J.; Sun, G.; Ellman, J. A.; Gallick, G.; Budde, R. J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Benzodiazepine Compounds as Inhibitors of the Src Protein Tyrosine Kinase: Screening of a Combinatorial Library of 1,4-BenzodiazepinesBenzodiazepine Compounds as Inhibitors of the Src Protein Tyrosine Kinase: Screening of a Combinatorial Library of 1,4-BenzodiazepinesBenzodiazepine compounds as inhibitors of the src protein tyrosine kinase: screening of a combinatorial library of 1, 4-benzodiazepines
year cv 199919991999
venue crossref Archives of Biochem. And Biophys.Archives of Biochemistry and BiophysicsArchives of Biochemistry and BiophysicsArchives of Biochemistry and Biophysics
kind cv articlearticleother
DOI crossref 10.1006/abbi.1999.131310.1006/abbi.1999.1313
first author openalex RamdasRamdasRamdas

Citations

OpenAlex
21
Scholar
33
DOI
10.1006/abbi.1999.1313
OpenAlex
W2041008865

Match decisions

  • doi merged · 1.00 · Run 18
1999 Chiral N-Acyl-tert-Butanesulfinamides: The “Safety-Catch” Principle Applied to Diastereoselective Enolate Alkylations The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 1167–1169 · CV · published

1167290. Backes, B. J.; Dragoli, D. R.; Ellman, J. A. “Chiral N-Acyl-tert-Butanesulfinamides: The “Safety-1168Catch” Principle Applied to Diastereoselective Enolate Alkylations” J. Org. Chem. 64, 5472-54781169(1999).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Dragoli, D. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Chiral N-Acyl-tert-Butanesulfinamides: The “Safety-Catch” Principle Applied to Diastereoselective Enolate AlkylationsChiral N -Acyl- tert -butanesulfinamides: The “Safety-Catch” Principle Applied to Diastereoselective Enolate AlkylationsChiral N-Acyl-tert-butanesulfinamides: The “Safety-Catch” Principle Applied to Diastereoselective Enolate Alkylations
year cv 199919991999
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo990271w10.1021/jo990271w
first author openalex BackesBackesBackes

Citations

OpenAlex
62
Scholar
81
DOI
10.1021/jo990271w
OpenAlex
W1966756269

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo990271w for chiral N-acyl-tert-butanesulfinamides.
  • doi merged · 1.00 · Run 18
1999 Combinatorial Library Approach to the Development of Synthetic Receptors Targeting Vancomycin Resistant Bacteria Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1171–1173 · CV · published

1171291. Xu, R.; Greiveldinger, G.; Marenus, L. E.; Cooper, A. G.; Ellman, J. A. “Combinatorial Library1172Approach to the Development of Synthetic Receptors Targeting Vancomycin Resistant Bacteria” J.1173Am. Chem. Soc. 121, 4898-4899 (1999).

Institution fields

Peer reviewed
yes
First author
Xu
Co-authors
Xu, R.; Greiveldinger, G.; Marenus, L. E.; Cooper, A. G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Library Approach to the Development of Synthetic Receptors Targeting Vancomycin Resistant BacteriaCombinatorial Library Approach for the Identification of Synthetic Receptors Targeting Vancomycin-Resistant BacteriaCombinatorial library approach for the identification of synthetic receptors targeting vancomycin-resistant bacteria
year cv 199919991999
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja990240i10.1021/ja990240i
first author openalex XuXuXu

Citations

OpenAlex
103
Scholar
144
DOI
10.1021/ja990240i
OpenAlex
W2093982102

Match decisions

  • doi merged · 1.00 · Run 18
1999 Compounds that activate the mouse melanocortin-1 receptor identified by screening a small molecule library based upon the β-turn Journal of medicinal chemistry article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title scholar Compounds that activate the mouse melanocortin-1 receptor identified by screening a small molecule library based upon the β-turn
year scholar 1999
venue scholar Journal of medicinal chemistry
kind scholar other
first author scholar Haskell-Luevano

Citations

OpenAlex
none
Scholar
95

Match decisions

No decision recorded; a single record.

1999 Expedient Synthesis of Alkoxylamines Using tert-Butyl Oxaziridine: The First Direct Amination of Alcohols J. Org. Chem. article journal CV OA GS

CV span

lines 1161–1162 · CV · published

1161288. Choong, I. C.; Ellman, J. A. “Expedient Synthesis of Alkoxylamines Using tert-Butyl Oxaziridine:1162The First Direct Amination of Alcohols” J. Org. Chem. 64, 6528-6529 (1999).

Institution fields

Peer reviewed
yes
First author
Choong
Co-authors
Choong, I. C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Expedient Synthesis of Alkoxylamines Using tert-Butyl Oxaziridine: The First Direct Amination of Alcohols
year cv 1999
venue cv J. Org. Chem.
kind cv article
first author cv Choong

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1999 Fmoc-BasedSynthesis of Peptide-Thioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical Ligation Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1138–1140 · CV · published

1138282. Shin, Y.; Winans, K. A.; Backes, B. J.; Kent, S. B. H.; Ellman, J. A.; Bertozzi, C. R. “Fmoc-1139BasedSynthesis of Peptide-Thioesters: Application to the Total Chemical Synthesis of a1140Glycoprotein by Native Chemical Ligation” J. Am. Chem. Soc. 121, 11684-11689 (1999).

Institution fields

Peer reviewed
yes
First author
Shin
Co-authors
Shin, Y.; Winans, K. A.; Backes, B. J.; Kent, S. B. H.; Ellman, J. A.; Bertozzi, C. R.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Fmoc-BasedSynthesis of Peptide-Thioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical LigationFmoc-Based Synthesis of Peptide-αThioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical LigationFmoc-based synthesis of peptide-αthioesters: application to the total chemical synthesis of a glycoprotein by native chemical ligation
year cv 199919991999
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja992881j10.1021/ja992881j
first author openalex ShinShinShin

Citations

OpenAlex
367
Scholar
484
DOI
10.1021/ja992881j
OpenAlex
W2027163628

Match decisions

  • doi merged · 1.00 · Run 18
1999 General Solid-phase Method for the Preparation of Mechanism-based Cysteine Protease Inhibitors Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1142–1143 · CV · published

1142283. Lee, A.; Huang, L.; Ellman, J. A. “General Solid-phase Method for the Preparation of Mechanism-1143based Cysteine Protease Inhibitors” J. Am. Chem. Soc. 121, 9907-9914 (1999).

Institution fields

Peer reviewed
yes
First author
Lee
Co-authors
Lee, A.; Huang, L.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General Solid-phase Method for the Preparation of Mechanism-based Cysteine Protease InhibitorsGeneral Solid-Phase Method for the Preparation of Mechanism-Based Cysteine Protease InhibitorsGeneral solid-phase method for the preparation of mechanism-based cysteine protease inhibitors
year cv 199919991999
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja992009a10.1021/ja992009a
first author openalex LeeLeeLee

Citations

OpenAlex
53
Scholar
93
DOI
10.1021/ja992009a
OpenAlex
W2011863201

Match decisions

  • doi merged · 1.00 · Run 18
1999 Identification of Agonists at the Human Melanocortin Receptor MC1R By the Evaluation of a Library of Small Molecules Based upon the -Turn J. Med. Chem. article journal CV OA GS

CV span

lines 1152–1154 · CV · published

1152286. Haskell-Leuvano, C.; Souers, A. J.; Rosenquist, A., Ellman, J. A.; Cone, R. D. “Identification of1153Agonists at the Human Melanocortin Receptor MC1R By the Evaluation of a Library of Small1154Molecules Based upon the -Turn” J. Med. Chem. 42, 4380-4387 (1999).

Institution fields

Peer reviewed
yes
First author
Haskell-Leuvano
Co-authors
Haskell-Leuvano, C.; Souers, A. J.; Rosenquist, A.; Ellman, J. A.; Cone, R. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Identification of Agonists at the Human Melanocortin Receptor MC1R By the Evaluation of a Library of Small Molecules Based upon the -Turn
year cv 1999
venue cv J. Med. Chem.
kind cv article
first author cv Haskell-Leuvano

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1999 Identification of a Potent Heterocyclic Ligand to Somatostatin Receptor Sub-Type 5 by the Synthesis and Screening of -Turn Mimetic Libraries Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1193–1195 · CV · published

1193297. Souers, A. J.; Virgilio, A. A.; Rosenquist, A.; Fenuik, W. Ellman, J. A. “Identification of a Potent1194Heterocyclic Ligand to Somatostatin Receptor Sub-Type 5 by the Synthesis and Screening of -1195Turn Mimetic Libraries” J. Am. Chem. Soc. 121, 1817-1825 (1999).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Virgilio, A. A.; Rosenquist, A.; Fenuik, W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Identification of a Potent Heterocyclic Ligand to Somatostatin Receptor Sub-Type 5 by the Synthesis and Screening of -Turn Mimetic LibrariesIdentification of a Potent Heterocyclic Ligand To Somatostatin Receptor Subtype 5 by the Synthesis and Screening of β-Turn Mimetic LibrariesIdentification of a potent heterocyclic ligand to somatostatin receptor subtype 5 by the synthesis and screening of β-turn mimetic libraries
year cv 199919991999
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja983742p10.1021/ja983742p
first author openalex SouersSouersSouers

Citations

OpenAlex
81
Scholar
118
DOI
10.1021/ja983742p
OpenAlex
W2008741858

Match decisions

  • doi merged · 1.00 · Run 18
1999 One-Pot Asymmetric Reductive Amination of Ketones to Prepare tert-Butanesulfinyl Protected Amines Tetrahedron Lett. article journal CV OA GS needs review

CV span

lines 1164–1165 · CV · published

1164289. Borg, G.; Cogan, D. A.; Ellman, J. A. “One-Pot Asymmetric Reductive Amination of Ketones to1165Prepare tert-Butanesulfinyl Protected Amines” Tetrahedron Lett. 40, 6709-6712 (1999).

Institution fields

Peer reviewed
yes
First author
Borg
Co-authors
Borg, G.; Cogan, D. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv One-Pot Asymmetric Reductive Amination of Ketones to Prepare tert-Butanesulfinyl Protected Amines
year cv 1999
venue cv Tetrahedron Lett.
kind cv article
first author cv Borg

Citations

OpenAlex
none
Scholar
none

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/s0040-4039(99)01351-9 for one-pot asymmetric synthesis of tert-butanesulfinyl-protected amines.
1999 One-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketimines Tetrahedron Letters article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex One-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketiminesOne-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketimines
year openalex 19991999
venue openalex Tetrahedron LettersTetrahedron letters
kind openalex articleother
DOI openalex 10.1016/s0040-4039(99)01351-9
first author openalex BorgBorg

Citations

OpenAlex
111
Scholar
146
DOI
10.1016/s0040-4039(99)01351-9
OpenAlex
W2048311189

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/s0040-4039(99)01351-9 for one-pot asymmetric synthesis of tert-butanesulfinyl-protected amines.
  • fingerprint merged · 1.00 · Run 18
1999 Parallel Solid-Phase Synthesis of Prostaglandin E Analogs Journal of Combinatorial Chemistry article journal CV OA GS

CV span

lines 1145–1146 · CV · published

1145284. Dragoli, D. R.; Ellman, J. A. “Parallel Solid-Phase Synthesis of Prostaglandin E Analogs” J. Comb.1146Chem. 1, 534-539 (1999).

Institution fields

Peer reviewed
yes
First author
Dragoli
Co-authors
Dragoli, D. R.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Parallel Solid-Phase Synthesis of Prostaglandin E AnalogsParallel Synthesis of Prostaglandin E1 AnaloguesParallel Synthesis of Prostaglandin E1 Analogues
year cv 199919991999
venue openalex J. Comb. Chem.Journal of Combinatorial ChemistryJournal of Combinatorial Chemistry
kind cv articlearticleother
DOI openalex 10.1021/cc990033e
first author openalex DragoliDragoliDragoli

Citations

OpenAlex
43
Scholar
74
DOI
10.1021/cc990033e
OpenAlex
W2081666794

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/cc990033e for parallel synthesis of prostaglandin E1 analogues.
1999 Pharmacophore Recombination for the Identification of Small Molecule Drug Lead Compounds PCT Int. Appl. reprint 2009 Pharmacophore recombination for the identification of small molecule drug lead compoundsversion 2002 Pharmacophore Recombination for the Identification of Small Molecule Drug Lead Compounds other CV OA GS

CV span

lines 1510–1511 · CV · published

151016. Ellman, J. A.; Choong, I. “Pharmacophore Recombination for the Identification of Small Molecule1511Drug Lead Compounds” PCT Int. Appl. (1999), WO 9949314 A1 19990930.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
Ellman, J. A.; Choong, I.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Pharmacophore Recombination for the Identification of Small Molecule Drug Lead Compounds
year cv 1999
venue cv PCT Int. Appl.
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1999 Preparation of Benzodiazepinones as Protein Tyrosine Kinase Inhibitors PCT Int. Appl. other CV OA GS

CV span

lines 1513–1515 · CV · published

151317. Budde, R, J. A.; Ellman, J. A.; Levin, V. A.; Gallick, G. E.; Newman, R. A.; “Preparation of1514Benzodiazepinones as Protein Tyrosine Kinase Inhibitors” PCT Int. Appl. (1999), WO 9919306 A2151519990422.

Institution fields

Peer reviewed
none
First author
Budde
Co-authors
Budde, R, J. A.; Ellman, J. A.; Levin, V. A.; Gallick, G. E.; Newman, R. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of Benzodiazepinones as Protein Tyrosine Kinase Inhibitors
year cv 1999
venue cv PCT Int. Appl.
kind cv other
first author cv Budde

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1999 Preparation of Enantioenriched -Bromo Acids with Diverse Side Chain Functionality Synthesis article journal CV OA GS needs review

CV span

lines 1186–1187 · CV · published

1186295. Souers, A. J.; Schürer, Kwack, H.; Virgilio, A. A.; Ellman, J. A. “Preparation of Enantioenriched1187-Bromo Acids with Diverse Side Chain Functionality” Synthesis, 583-585 (1999).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Schürer; Kwack, H.; Virgilio, A. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Preparation of Enantioenriched -Bromo Acids with Diverse Side Chain Functionality
year cv 1999
venue cv Synthesis
kind cv article
first author cv Souers

Citations

OpenAlex
none
Scholar
none

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1055/s-1999-3427 for preparation of enantioenriched alpha-bromo acids.
1999 Preparation of Enantioenriched α-Bromo Acids Incorporating Diverse Functionality Synthesis article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Preparation of Enantioenriched α-Bromo Acids Incorporating Diverse FunctionalityPreparation of enantioenriched α-bromo acids incorporating diverse functionality
year openalex 19991999
venue openalex SynthesisSynthesis
kind openalex articleother
DOI openalex 10.1055/s-1999-3427
first author openalex SouersSouers

Citations

OpenAlex
18
Scholar
27
DOI
10.1055/s-1999-3427
OpenAlex
W2949960908

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1055/s-1999-3427 for preparation of enantioenriched alpha-bromo acids.
  • fingerprint merged · 1.00 · Run 18
1999 Single Digit Nanomolar, Low Molecular Weight Non-Peptide Inhibitors of Malarial Aspartyl Protease Plasmepsin II Journal of Medicinal Chemistry article journal CV OA GS

CV span

lines 1179–1181 · CV · published

1179293. Haque, T. S.; Skillman, A. G.; Lee, C. E.; Habashita, H.; Gluzman, I. Y.; Ewing, T. J. A.; Goldberg,1180D. E.; Kuntz, I. D.; Ellman, J. A. “Single Digit Nanomolar, Low Molecular Weight Non-Peptide1181Inhibitors of Malarial Aspartyl Protease Plasmepsin II” J. Med. Chem. 42, 1428-1440 (1999).

Institution fields

Peer reviewed
yes
First author
Haque
Co-authors
Haque, T. S.; Skillman, A. G.; Lee, C. E.; Habashita, H.; Gluzman, I. Y.; Ewing, T. J. A.; Goldberg, D. E.; Kuntz, I. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Single Digit Nanomolar, Low Molecular Weight Non-Peptide Inhibitors of Malarial Aspartyl Protease Plasmepsin IIPotent, Low-Molecular-Weight Non-Peptide Inhibitors of Malarial Aspartyl Protease Plasmepsin IIPotent, low-molecular-weight non-peptide inhibitors of malarial aspartyl protease plasmepsin II
year cv 199919991999
venue crossref J. Med. Chem.Journal of Medicinal ChemistryJournal of Medicinal ChemistryJournal of Medicinal Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jm980641t10.1021/jm980641t
first author openalex HaqueHaqueHaque

Citations

OpenAlex
169
Scholar
234
DOI
10.1021/jm980641t
OpenAlex
W2093094597

Match decisions

  • doi merged · 1.00 · Run 18
1999 Synthesis of Alkoxylamines by Alkoxide Amination with 3,3‘-Di- tert -butyloxaziridine The Journal of Organic Chemistry article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Synthesis of Alkoxylamines by Alkoxide Amination with 3,3‘-Di- tert -butyloxaziridineSynthesis of Alkoxylamines by Alkoxide Amination with 3,3‘-Di-tert-butyloxaziridine
year openalex 19991999
venue openalex The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind openalex articleother
DOI openalex 10.1021/jo990490h
first author openalex ChoongChoong

Citations

OpenAlex
54
Scholar
77
DOI
10.1021/jo990490h
OpenAlex
W1977855028

Match decisions

  • fingerprint merged · 1.00 · Run 18
1999 The Asymmetric Synthesis of -Dibranched Amines by the Trimethylaluminum Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl Ketimines Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1197–1199 · CV · published

1197298. Cogan, D. A.; Ellman, J. A. “The Asymmetric Synthesis of -Dibranched Amines by the1198Trimethylaluminum Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl Ketimines” J.1199Am. Chem. Soc. 121, 268-269 (1999).

Institution fields

Peer reviewed
yes
First author
Cogan
Co-authors
Cogan, D. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Asymmetric Synthesis of -Dibranched Amines by the Trimethylaluminum Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl KetiminesAsymmetric Synthesis of α,α-Dibranched Amines by the Trimethylaluminum-Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl KetiminesAsymmetric synthesis of α, α-dibranched amines by the trimethylaluminum-mediated 1, 2-addition of organolithiums to tert-butanesulfinyl ketimines
year cv 199919981999
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja983217q10.1021/ja983217q
first author openalex CoganCoganCogan

Citations

OpenAlex
239
Scholar
308
DOI
10.1021/ja983217q
OpenAlex
W2037764504

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja983217q for asymmetric synthesis of alpha,alpha-dibranched amines.
  • doi merged · 1.00 · Run 18
1999 The Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 1189–1192 · CV · published

1189296. Liu, G.; Cogan, D. A.; Owens, T. D.; Tang, T. P.; Ellman, J. A. “The Synthesis of Enantiomerically1190Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-1191Butanesulfinamide with Aldehydes and Ketones” J. Org. Chem. 64,1278-1284 (1999).1192

Institution fields

Peer reviewed
yes
First author
Liu
Co-authors
Liu, G.; Cogan, D. A.; Owens, T. D.; Tang, T. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and KetonesSynthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and KetonesSynthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones
year cv 199919991999
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo982059i10.1021/jo982059i
first author openalex LiuLiuLiu

Citations

OpenAlex
504
Scholar
709
DOI
10.1021/jo982059i
OpenAlex
W2158192184

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo982059i for synthesis of N-tert-butanesulfinyl imines.
  • doi merged · 1.00 · Run 18
1999 The tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for Asymmetric -Amino Acid Synthesis and Applications The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 1201–1203 · CV · published

1201299. Tang, T. P.; Ellman, J. A. “The tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and1202Boc-Surrogate for Asymmetric -Amino Acid Synthesis and Applications” J. Org. Chem. 64, 12-120313 (1999).

Institution fields

Peer reviewed
yes
First author
Tang
Co-authors
Tang, T. P.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for Asymmetric -Amino Acid Synthesis and ApplicationsThe tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for the Asymmetric Synthesis and Applications of β-Amino AcidsThe tert-butanesulfinyl group: an ideal chiral directing group and Boc-surrogate for the asymmetric synthesis and applications of β-amino acids
year cv 199919981999
venue crossref J. Org. Chem.The Journal of Organic ChemistryJ. Org. ChemThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo982082410.1021/jo9820824
first author openalex TangTangTang

Citations

OpenAlex
174
Scholar
294
DOI
10.1021/jo9820824
OpenAlex
W1988446650

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jo9820824 for the tert-butanesulfinyl group in beta-amino acid synthesis.
  • doi merged · 1.00 · Run 18
1998 Catalytic Asymmetric Oxidation of tert-Butyl Disulfide. Synthesis of tert-Butanesulfinamides, tert-Butyl Sulfoxide, and tert-Butanesulfinimines Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1216–1218 · CV · published

1216303. Cogan, D. A.; Liu, G.; Kim, K.; Backes, B. A.; Ellman, J. A. “Catalytic Asymmetric Oxidation of1217tert-Butyl Disulfide. Synthesis of tert-Butanesulfinamides, tert-Butyl Sulfoxide, and tert-1218Butanesulfinimines” J. Am. Chem. Soc. 120, 8011-8019 (1998).

Institution fields

Peer reviewed
yes
First author
Cogan
Co-authors
Cogan, D. A.; Liu, G.; Kim, K.; Backes, B. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Asymmetric Oxidation of tert-Butyl Disulfide. Synthesis of tert-Butanesulfinamides, tert-Butyl Sulfoxide, and tert-ButanesulfiniminesCatalytic Asymmetric Oxidation oftert-Butyl Disulfide. Synthesis oftert-Butanesulfinamides,tert-Butyl Sulfoxides, andtert-Butanesulfinimines
year cv 19981998
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticle
DOI crossref 10.1021/ja980920610.1021/ja9809206
first author openalex CoganCogan

Citations

OpenAlex
361
Scholar
none
DOI
10.1021/ja9809206
OpenAlex
W1965128725

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja9809206 for catalytic asymmetric oxidation of tert-butyl disulfide.
  • doi merged · 1.00 · Run 18
1998 ChemInform Abstract: Catalytic Asymmetric Oxidation of tert‐Butyl Disulfide. Synthesis of tert‐Butanesulfinamides, tert‐Butyl Sulfoxides, and tert‐Butanesulfinimines. ChemInform article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex ChemInform Abstract: Catalytic Asymmetric Oxidation of tert‐Butyl Disulfide. Synthesis of tert‐Butanesulfinamides, tert‐Butyl Sulfoxides, and tert‐Butanesulfinimines.Catalytic asymmetric oxidation of tert-butyl disulfide. Synthesis of tert-butanesulfinamides, tert-butyl sulfoxides, and tert-butanesulfinimines
year openalex 19981998
venue openalex ChemInformJournal of the American Chemical Society
kind openalex articleother
DOI openalex 10.1002/chin.199851041
first author openalex CoganCogan

Citations

OpenAlex
0
Scholar
479
DOI
10.1002/chin.199851041
OpenAlex
W2949205688

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja9809206 for catalytic asymmetric oxidation of tert-butyl disulfide.
  • fingerprint merged · 1.00 · Run 18
1998 Combinatorial Chemistry Current Opinion in Chemical Biology reprint 1997 Combinatorial Chemistry article journal CV OA GS

CV span

lines 1220–1221 · CV · published

1220304. Ellman, J. A.; Gallop, M. A. “Combinatorial Chemistry” Curr. Opin. Chem. Biol. 2, 317-3191221(1998).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J. A.; Gallop, M. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Chemistry
year cv 1998
venue crossref Curr. Opin. Chem. Biol.Current Opinion in Chemical Biology
kind cv article
DOI crossref 10.1016/s1367-5931(98)80003-3
first author cv Ellman

Citations

OpenAlex
none
Scholar
none
DOI
10.1016/s1367-5931(98)80003-3

Match decisions

No decision recorded; a single record.

1998 Conformationally Restricted Peptide and Peptidomimetic Libraries Combinatorial Chemistry and Molecular Diversity in Drug Discovery chapter CV OA GS

CV span

lines 1285–1287 · CV · published

1285323. Virgilio, A. A.; Ellman, J. A. "Conformationally Restricted Peptide and Peptidomimetic Libraries"1286in Combinatorial Chemistry and Molecular Diversity in Drug Discovery; Gordon, E. M. and1287Kerwin, J. F. Ed.; John Wiley & Sons, Inc.: New York, New York, 1998, pp. 133-151.

Institution fields

Peer reviewed
none
First author
Virgilio
Co-authors
Virgilio, A. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
John Wiley & Sons, Inc.
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Conformationally Restricted Peptide and Peptidomimetic Libraries
year cv 1998
venue cv Combinatorial Chemistry and Molecular Diversity in Drug Discovery
kind cv chapter
first author cv Virgilio

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1998 General Solid-Phase Synthesis Approach to Prepare Mechanism-Based Aspartyl Protease Inhibitor Libraries. Identification of Potent Cathepsin D Inhibitors Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1208–1210 · CV · published

1208301. Lee, C. E.; Kick, E. K.; Ellman, J. A. “General Solid-Phase Synthesis Approach to Prepare1209Mechanism-Based Aspartyl Protease Inhibitor Libraries. Identification of Potent Cathepsin D1210Inhibitors” J. Am. Chem. Soc. 120, 9735-9748 (1998).

Institution fields

Peer reviewed
yes
First author
Lee
Co-authors
Lee, C. E.; Kick, E. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General Solid-Phase Synthesis Approach to Prepare Mechanism-Based Aspartyl Protease Inhibitor Libraries. Identification of Potent Cathepsin D InhibitorsGeneral Solid-Phase Synthesis Approach To Prepare Mechanism-Based Aspartyl Protease Inhibitor Libraries. Identification of Potent Cathepsin D InhibitorsGeneral solid-phase synthesis approach to prepare mechanism-based aspartyl protease inhibitor libraries. Identification of potent cathepsin D inhibitors
year cv 199819981998
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja981812m10.1021/ja981812m
first author openalex LeeLeeLee

Citations

OpenAlex
55
Scholar
110
DOI
10.1021/ja981812m
OpenAlex
W2014714297

Match decisions

  • doi merged · 1.00 · Run 18
1998 Novel Inhibitors of 41 Integrin Receptor Interactions Through Library Synthesis and Screening Bioorganic &amp; Medicinal Chemistry Letters article journal CV OA GS

CV span

lines 1212–1214 · CV · published

1212302. Souers, A. J.; Virgilio, A. A.; Schürer, S. S.; Ellman, J. A.; Vanderslice, P.; Kogan, T. P. “Novel1213Inhibitors of 41 Integrin Receptor Interactions Through Library Synthesis and Screening”1214BioMed. Chem. Lett. 8, 2297-2303 (1998).

Institution fields

Peer reviewed
yes
First author
Souers
Co-authors
Souers, A. J.; Virgilio, A. A.; Schürer, S. S.; Ellman, J. A.; Vanderslice, P.; Kogan, T. P.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Novel Inhibitors of 41 Integrin Receptor Interactions Through Library Synthesis and ScreeningNovel inhibitors of α4β1 integrin receptor interactions through library synthesis and screeningNovel inhibitors of α4β1 integrin receptor interactions through library synthesis and screening
year cv 199819981998
venue crossref BioMed. Chem. Lett.Bioorganic & Medicinal Chemistry LettersBioorganic & medicinal chemistry lettersBioorganic &amp; Medicinal Chemistry Letters
kind cv articlearticleother
DOI crossref 10.1016/s0960-894x(98)00416-810.1016/s0960-894x(98)00416-8
first author openalex SouersSouersSouers

Citations

OpenAlex
48
Scholar
75
DOI
10.1016/s0960-894x(98)00416-8
OpenAlex
W2091305367

Match decisions

  • doi merged · 1.00 · Run 18
1998 Solid-Phase Synthesis of Diverse E- F-Series Prostaglandins The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1223–1224 · CV · published

1223305. Thompson, L. A.; Moore, F. L.; Moon, Y.-C; Ellman, J. A. “Solid-Phase Synthesis of Diverse E- F-1224Series Prostaglandins” J. Org. Chem. 63, 2066-2067 (1998).

Institution fields

Peer reviewed
yes
First author
Thompson
Co-authors
Thompson, L. A.; Moore, F. L.; Moon, Y.-C; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Solid-Phase Synthesis of Diverse E- F-Series ProstaglandinsSolid-Phase Synthesis of Diverse E- and F-Series ProstaglandinsSolid-phase synthesis of diverse E-and F-series prostaglandins
year cv 199819981998
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo980076210.1021/jo9800762
first author openalex ThompsonThompsonThompson

Citations

OpenAlex
56
Scholar
100
DOI
10.1021/jo9800762
OpenAlex
W2063854225

Match decisions

  • doi merged · 1.00 · Run 18
1998 Synthesis of 3-Substituted 1,4-Benzodiazepin-2-ones Journal of the Brazilian Chemical Society article journal CV OA GS

CV span

lines 1205–1206 · CV · published

1205300. Kim, K.; Volkman, S. K.; Ellman, J. A. “Synthesis of 3-Substituted 1,4-Benzodiazepin-2-ones” J.1206Braz. Chem. Soc. 9, 375-379 (1998).

Institution fields

Peer reviewed
yes
First author
Kim
Co-authors
Kim, K.; Volkman, S. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis of 3-Substituted 1,4-Benzodiazepin-2-onesSynthesis of 3-Substituted 1,4-Benzodiazepin-2-onesSynthesis of 3-substituted 1, 4-benzodiazepin-2-ones
year cv 199819981998
venue crossref J. Braz. Chem. Soc.Journal of the Brazilian Chemical SocietyJournal of the Brazilian Chemical SocietyJournal of the Brazilian Chemical Society
kind cv articlearticleother
DOI crossref 10.1590/s0103-5053199800040001010.1590/s0103-50531998000400010
first author openalex KimKyungjinKyungjin

Citations

OpenAlex
18
Scholar
51
DOI
10.1590/s0103-50531998000400010
OpenAlex
W2071298232

Match decisions

  • doi merged · 1.00 · Run 18
1997 Approaches to the Synthesis of the Vancomycin Antibiotics. Synthesis of Orienticin C (Bis-dechlorovancomycin) Aglycon Journal of the American Chemical Society article journal CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex Approaches to the Synthesis of the Vancomycin Antibiotics. Synthesis of Orienticin C (Bis-dechlorovancomycin) AglyconApproaches to the synthesis of the vancomycin antibiotics. Synthesis of orienticin C (bis-dechlorovancomycin) aglycon
year openalex 19971997
venue openalex Journal of the American Chemical SocietyJournal of the American Chemical Society
kind openalex articleother
DOI openalex 10.1021/ja964420t
first author openalex EvansEvans

Citations

OpenAlex
79
Scholar
109
DOI
10.1021/ja964420t
OpenAlex
W2161016813

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja964420t for vancomycin antibiotics synthesis.
  • fingerprint merged · 1.00 · Run 18
1997 A Silicon Linker for the Direct Loading of Aromatic Compounds onto Solid Supports. Traceless Synthesis of Pyridyl-Based Tricyclics The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1226–1228 · CV · published

1226306. Woolard, F. X.; Paetsch, J.; Ellman, J. A. “A Silicon Linker for the Direct Loading of Aromatic1227Compounds onto Solid Supports. Traceless Synthesis of Pyridyl-Based Tricyclics” J. Org. Chem.122862, 6102-6103 (1997).

Institution fields

Peer reviewed
yes
First author
Woolard
Co-authors
Woolard, F. X.; Paetsch, J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Silicon Linker for the Direct Loading of Aromatic Compounds onto Solid Supports. Traceless Synthesis of Pyridyl-Based TricyclicsA Silicon Linker for Direct Loading of Aromatic Compounds to Supports. Traceless Synthesis of Pyridine-Based TricyclicsA silicon linker for direct loading of aromatic compounds to supports. Traceless synthesis of pyridine-based tricyclics
year cv 199719971997
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo971074510.1021/jo9710745
first author openalex WoolardWoolardWoolard

Citations

OpenAlex
86
Scholar
138
DOI
10.1021/jo9710745
OpenAlex
W2074714235

Match decisions

  • doi merged · 1.00 · Run 18
1997 Catalytic Asymmetric Synthesis of tert-Butanesulfinamide. Application to the Asymmetric Synthesis of Amines Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1230–1231 · CV · published

1230307. Liu, G.; Cogan, D. A.; Ellman, J. A. “Catalytic Asymmetric Synthesis of tert-Butanesulfinamide.1231Application to the Asymmetric Synthesis of Amines” J. Am. Chem. Soc. 119, 9913-9914 (1997).

Institution fields

Peer reviewed
yes
First author
Liu
Co-authors
Liu, G.; Cogan, D. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Catalytic Asymmetric Synthesis of tert-Butanesulfinamide. Application to the Asymmetric Synthesis of AminesCatalytic Asymmetric Synthesis of tert-Butanesulfinamide. Application to the Asymmetric Synthesis of AminesCatalytic asymmetric synthesis of tert-butanesulfinamide. Application to the asymmetric synthesis of amines
year cv 199719971997
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja972012z10.1021/ja972012z
first author openalex LiuLiuLiu

Citations

OpenAlex
519
Scholar
788
DOI
10.1021/ja972012z
OpenAlex
W1996768696

Match decisions

  • doi merged · 1.00 · Run 18
1997 Combinatorial Thinking in Chemistry and Biology Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 1246–1247 · CV · published

1246312. Ellman, J. Stoddard, B.; Wells, J. “Combinatorial Thinking in Chemistry and Biology” Proc. Natl.1247Acad. Sci., USA 94, 2779-2782 (1997).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J.; Stoddard, B.; Wells, J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Thinking in Chemistry and BiologyCombinatorial thinking in chemistry and biologyCombinatorial thinking in chemistry and biology
year cv 199719971997
venue crossref Proc. Natl. Acad. Sci., USAProceedings of the National Academy of SciencesProceedings of the National Academy of SciencesProceedings of the National Academy of Sciences
kind cv articlearticleother
DOI crossref 10.1073/pnas.94.7.277910.1073/pnas.94.7.2779
first author openalex EllmanEllmanEllman

Citations

OpenAlex
42
Scholar
89
DOI
10.1073/pnas.94.7.2779
OpenAlex
W2017662385

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the exact DOI 10.1073/pnas.94.7.2779 and title for combinatorial thinking in chemistry and biology.
1997 Germanium and Silicon Linking Strategies for Traceless Solid-Phase Synthesis The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1243–1244 · CV · published

1243311. Plunkett, M. J.; Ellman, J. A. "Germanium and Silicon Linking Strategies for Traceless Solid-Phase1244Synthesis" J. Org. Chem. 62, 2885-2893 (1997).

Institution fields

Peer reviewed
yes
First author
Plunkett
Co-authors
Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Germanium and Silicon Linking Strategies for Traceless Solid-Phase SynthesisGermanium and Silicon Linking Strategies for Traceless Solid-Phase SynthesisGermanium and silicon linking strategies for traceless solid-phase synthesis
year cv 199719971997
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo961889y10.1021/jo961889y
first author openalex PlunkettPlunkettPlunkett

Citations

OpenAlex
133
Scholar
193
DOI
10.1021/jo961889y
OpenAlex
W2041712015

Match decisions

  • doi merged · 1.00 · Run 18
1997 Solid Support Linker Strategies ChemInform article journal CV OA GS needs review

CV span

lines 1233–1234 · CV · published

1233308. Backes, B. A.; Ellman, J. A. “Solid Support Linker Strategies” Curr. Opin. Chem. Biol. 1, 86-941234(1997).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. A.; Ellman, J. A.
Subfield
other
Method
review
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Solid Support Linker StrategiesChemInform Abstract: Design, Synthesis, and Evaluation of Small‐Molecule LibrariesChemInform Abstract: Solid‐Phase Synthesis: Applications to Combinatorial LibrariesChemInform Abstract: Carbon‐Carbon Bond‐Forming Methods on Solid Support. Utilization of Kenner′s “Safety‐Catch” Linker.ChemInform Abstract: Catalytic Asymmetric Synthesis of tert‐Butanesulfinamide. Application to the Asymmetric Synthesis of Amines.ChemInform Abstract: Synthesis and Applications of Small Molecule LibrariesChemInform Abstract: Approaches to the Synthesis of the Vancomycin Antibiotics. Synthesis of Orienticin C (Bis‐dechlorovancomycin) Aglycon (I).ChemInform Abstract: Solid‐Support Linker StrategiesChemInform Abstract: Synthesis and Evaluation of 1,4‐Benzodiazepine LibrariesChemInform Abstract: Synthesis and Evaluation of Three 1,4‐Benzodiazepine LibrariesSolid support linker strategies
year cv 19971996199719951998199619971997199719971997
venue crossref Curr. Opin. Chem. Biol.ChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformChemInformCurrent Opinion in Chemical BiologyChemInform
kind cv articlearticlearticlearticlearticlearticlearticlearticlearticlearticleother
DOI crossref 10.1002/chin.19974233110.1002/chin.19962732510.1002/chin.19971432110.1002/chin.19951906510.1002/chin.19980502610.1002/chin.19962229610.1002/chin.19973428210.1002/chin.19974233110.1002/chin.19970627210.1002/chin.199747307
first author openalex BackesEllmanChoongBackesLiuThompsonEvansBackesBuninBuninBackes

Also recorded as

  • W1994997006 (DOI 10.1002/chin.199627325) · platform twin · 1996 ChemInform Abstract: Design, Synthesis, and Evaluation of Small‐Molecule Libraries
  • W2013564348 (DOI 10.1002/chin.199714321) · platform twin · 1997 ChemInform Abstract: Solid‐Phase Synthesis: Applications to Combinatorial Libraries
  • W2140500955 (DOI 10.1002/chin.199519065) · title variant · 1995 ChemInform Abstract: Carbon‐Carbon Bond‐Forming Methods on Solid Support. Utilization of Kenner′s “Safety‐Catch” Linker.
  • W2950546706 (DOI 10.1002/chin.199805026) · platform twin · 1998 ChemInform Abstract: Catalytic Asymmetric Synthesis of tert‐Butanesulfinamide. Application to the Asymmetric Synthesis of Amines.
  • W2951344643 (DOI 10.1002/chin.199622296) · platform twin · 1996 ChemInform Abstract: Synthesis and Applications of Small Molecule Libraries
  • W2951813905 (DOI 10.1002/chin.199734282) · platform twin · 1997 ChemInform Abstract: Approaches to the Synthesis of the Vancomycin Antibiotics. Synthesis of Orienticin C (Bis‐dechlorovancomycin) Aglycon (I).
  • W2952240050 (DOI 10.1002/chin.199706272) · platform twin · 1997 ChemInform Abstract: Synthesis and Evaluation of 1,4‐Benzodiazepine Libraries
  • W4242040752 (DOI 10.1002/chin.199747307) · platform twin · 1997 ChemInform Abstract: Synthesis and Evaluation of Three 1,4‐Benzodiazepine Libraries

Citations

OpenAlex
0
Scholar
104
DOI
10.1002/chin.199742331
OpenAlex
W2952232592

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja964420t for vancomycin antibiotics synthesis.
  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/cr9402081 for synthesis and applications of small molecule libraries.
  • doi merged · 1.00 · Run 18
1997 Structure-Based Design and Combinatorial Chemistry Yield Low Nanomolar Inhibitors of Cathepsin D Chemistry &amp; Biology article journal CV OA GS

CV span

lines 1236–1238 · CV · published

1236309. Kick, E. K.; Roe, D. C.; Skillman, A. G.; Liu, G.; Ewing, T. J. A.; Sun, Y.; Kuntz, I. D.; Ellman, J.1237A. “Structure-Based Design and Combinatorial Chemistry Yield Low Nanomolar Inhibitors of1238Cathepsin D” Chem. Biol. 4, 297-309 (1997).

Institution fields

Peer reviewed
yes
First author
Kick
Co-authors
Kick, E. K.; Roe, D. C.; Skillman, A. G.; Liu, G.; Ewing, T. J. A.; Sun, Y.; Kuntz, I. D.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Structure-Based Design and Combinatorial Chemistry Yield Low Nanomolar Inhibitors of Cathepsin DStructure-based design and combinatorial chemistry yield low nanomolar inhibitors of cathepsin D
year cv 19971997
venue crossref Chem. Biol.Chemistry & biologyChemistry &amp; Biology
kind cv articleother
DOI crossref 10.1016/s1074-5521(97)90073-9
first author cv KickKick

Citations

OpenAlex
none
Scholar
267
DOI
10.1016/s1074-5521(97)90073-9

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the exact DOI 10.1073/pnas.94.7.2779 and title for combinatorial thinking in chemistry and biology.
1997 Synthesis and Conformational Properties of the M(4-6)(5-7) Bicyclic Tetrapeptide Common to the Vancomycin Antibiotics J. Am. Chem. Soc. article journal CV OA GS

CV span

lines 1249–1252 · CV · published

1249313. Evans, D. A.; Barrow, J. C.; Watson, P. S.; Ratz, A. M.; Dinsmore, C. J.; Evrard, D. A.; DeVries,1250K.; Ellman, J. A.; Rychnovsky, S. D.; Lacour, J. “Synthesis and Conformational Properties of the1251M(4-6)(5-7) Bicyclic Tetrapeptide Common to the Vancomycin Antibiotics” J. Am. Chem. Soc.1252119, 3419-3420 (1997).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A.; Barrow, J. C.; Watson, P. S.; Ratz, A. M.; Dinsmore, C. J.; Evrard, D. A.; DeVries, K.; Ellman, J. A.; Rychnovsky, S. D.; Lacour, J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Synthesis and Conformational Properties of the M(4-6)(5-7) Bicyclic Tetrapeptide Common to the Vancomycin Antibiotics
year cv 1997
venue cv J. Am. Chem. Soc.
kind cv article
first author cv Evans

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1997 Synthesis and Evaluation of a Library of Peptidomimetics Based upon the -Turn Tetrahedron article journal CV OA GS

CV span

lines 1240–1241 · CV · published

1240310. Virgilio, A. A.; Bray, A. A.; Zhang, W.; Ellman, J. A. "Synthesis and Evaluation of a Library of1241Peptidomimetics Based upon the -Turn" Tetrahedron 53, 6635-6644 (1997).

Institution fields

Peer reviewed
yes
First author
Virgilio
Co-authors
Virgilio, A. A.; Bray, A. A.; Zhang, W.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Synthesis and Evaluation of a Library of Peptidomimetics Based upon the -TurnSynthesis and evaluation of a library of peptidomimetics based upon the β-turnSynthesis and evaluation of a library of peptidomimetics based upon the β-turn
year cv 199719971997
venue crossref TetrahedronTetrahedronTetrahedron
kind cv articlearticleother
DOI crossref 10.1016/s0040-4020(97)00221-410.1016/s0040-4020(97)00221-4
first author openalex VirgilioVirgilioVirgilio

Citations

OpenAlex
41
Scholar
60
DOI
10.1016/s0040-4020(97)00221-4
OpenAlex
W2092400325

Match decisions

  • doi merged · 1.00 · Run 18
1997 The Solid-Phase Synthesis of 1,4-Benzodiazepine-2,5-diones. Library Preparation and Demonstration of Synthesis Generality The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1254–1256 · CV · published

1254314. Boojamra, C. G.; Burow, K. M.; Thompson, L. A.; Ellman, J. A. "The Solid-Phase Synthesis of12551,4-Benzodiazepine-2,5-diones. Library Preparation and Demonstration of Synthesis Generality" J.1256Org. Chem. 62, 1240-1257 (1997).

Institution fields

Peer reviewed
yes
First author
Boojamra
Co-authors
Boojamra, C. G.; Burow, K. M.; Thompson, L. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Solid-Phase Synthesis of 1,4-Benzodiazepine-2,5-diones. Library Preparation and Demonstration of Synthesis GeneralitySolid-Phase Synthesis of 1,4-Benzodiazepine-2,5-diones. Library Preparation and Demonstration of Synthesis GeneralitySolid-phase synthesis of 1, 4-benzodiazepine-2, 5-diones. Library preparation and demonstration of synthesis generality
year cv 199719971997
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo962284510.1021/jo9622845
first author openalex BoojamraBoojamraBoojamra

Citations

OpenAlex
163
Scholar
251
DOI
10.1021/jo9622845
OpenAlex
W2082491230

Match decisions

  • doi merged · 1.00 · Run 18
1997 The Synthesis of a 1680 Compound 1,4-Benzodiazepine Library New J. Chem. article journal CV OA GS

CV span

lines 1265–1266 · CV · published

1265317. Bunin, B. A.; Plunkett, M. J.; Bray, A. M.; Ellman, J. A. "The Synthesis of a 1680 Compound 1,4-1266Benzodiazepine Library" New J. Chem. 21, 125 (1997).

Institution fields

Peer reviewed
yes
First author
Bunin
Co-authors
Bunin, B. A.; Plunkett, M. J.; Bray, A. M.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv The Synthesis of a 1680 Compound 1,4-Benzodiazepine LibraryThe synthesis of a 1680 member 1, 4-benzodiazepine library
year cv 19971997
venue cv New J. Chem.New journal of chemistry
kind cv articleother
first author cv BuninBunin

Citations

OpenAlex
none
Scholar
37

Match decisions

  • fingerprint merged · 1.00 · Run 18
1996 Activation Method to Prepare a Highly Reactive Acylsulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1278–1280 · CV · published

1278321. Backes, B. J.; Virgilio, A. A.; Ellman, J. A. "Activation Method to Prepare a Highly Reactive1279Acylsulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis" J. Am. Chem. Soc. 118, 3055-12803057 (1996).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Virgilio, A. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Activation Method to Prepare a Highly Reactive Acylsulfonamide “Safety-Catch” Linker for Solid-Phase SynthesisActivation Method to Prepare a Highly Reactive Acylsulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis1Activation Method to Prepare a Highly Reactive Acylsulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis1
year cv 199619961996
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja953516510.1021/ja9535165
first author openalex BackesBackesBackes

Citations

OpenAlex
253
Scholar
336
DOI
10.1021/ja9535165
OpenAlex
W2029680398

Match decisions

  • doi merged · 1.00 · Run 18
1996 Design, Synthesis, and Evaluation of Small-Molecule Libraries Accounts of Chemical Research article journal CV OA GS needs review

CV span

lines 1292–1293 · CV · published

1292325. Ellman, J. A. "Design, Synthesis, and Evaluation of Small-Molecule Libraries" Acc. Chem. Res. 29,1293132-143 (1996).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Design, Synthesis, and Evaluation of Small-Molecule LibrariesDesign, Synthesis, and Evaluation of Small-Molecule LibrariesDesign, synthesis, and evaluation of small-molecule libraries
year cv 199619961996
venue crossref Acc. Chem. Res.Accounts of Chemical ResearchAccounts of chemical researchAccounts of Chemical Research
kind cv articlearticleother
DOI crossref 10.1021/ar950190w10.1021/ar950190w
first author openalex EllmanEllmanEllman

Citations

OpenAlex
289
Scholar
386
DOI
10.1021/ar950190w
OpenAlex
W2949206075

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/cr9402081 for synthesis and applications of small molecule libraries.
  • doi merged · 1.00 · Run 18
1996 Expedient Synthesis of -Turn Mimetics Incorporating the i + 1, i + 2, and i + 3 Sidechains Tetrahedron Letters article journal CV OA GS

CV span

lines 1275–1276 · CV · published

1275320. Virgilio, A. A.; Schürer, S.; Ellman, J. A. "Expedient Synthesis of -Turn Mimetics Incorporating1276the i + 1, i + 2, and i + 3 Sidechains" Tetrahedron Lett. 37, 6961-6964 (1996).

Institution fields

Peer reviewed
yes
First author
Virgilio
Co-authors
Virgilio, A. A.; Schürer, S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Expedient Synthesis of -Turn Mimetics Incorporating the i + 1, i + 2, and i + 3 SidechainsExpedient solid-phase synthesis of putative β-turn mimetics incorporating the i + 1, i + 2, and i + 3 sidechainsExpedient solid-phase synthesis of putative β-turn mimetics incorporating the i+ 1, i+ 2, and i+ 3 sidechains
year cv 199619961996
venue crossref Tetrahedron Lett.Tetrahedron LettersTetrahedron lettersTetrahedron Letters
kind cv articlearticleother
DOI crossref 10.1016/0040-4039(96)01572-910.1016/0040-4039(96)01572-9
first author openalex VirgilioVirgilioVirgilio

Citations

OpenAlex
72
Scholar
101
DOI
10.1016/0040-4039(96)01572-9
OpenAlex
W1982083227

Match decisions

  • doi merged · 1.00 · Run 18
1996 Non-Nucleic Acid Inhibitors of Protein-DNA Interactions Identified through Combinatorial Chemistry Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1271–1273 · CV · published

1271319. Stevens, S. Y.; Bunin, B. A.; Plunkett, M. J.; Swanson, P. C.; Ellman, J. A.; Glick, G. D. "Non-1272Nucleic Acid Inhibitors of Protein-DNA Interactions Identified through Combinatorial Chemistry"1273J. Am. Chem. Soc. 118, 10650-10651 (1996).

Institution fields

Peer reviewed
yes
First author
Stevens
Co-authors
Stevens, S. Y.; Bunin, B. A.; Plunkett, M. J.; Swanson, P. C.; Ellman, J. A.; Glick, G. D.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Non-Nucleic Acid Inhibitors of Protein-DNA Interactions Identified through Combinatorial ChemistryNon Nucleic Acid Inhibitors of Protein·DNA Interactions Identified through Combinatorial ChemistryNon nucleic acid inhibitors of protein· DNA interactions identified through combinatorial chemistry
year cv 199619961996
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja962452a10.1021/ja962452a
first author openalex StevensStevensStevens

Citations

OpenAlex
20
Scholar
57
DOI
10.1021/ja962452a
OpenAlex
W1998487003

Match decisions

  • doi merged · 1.00 · Run 18
1996 Palladium-Mediated Three-Component Coupling Strategy for the Solid-Phase Synthesis of Tropane Derivatives The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1282–1283 · CV · published

1282322. Koh, J. S.; Ellman, J. A. "Palladium-Mediated Three-Component Coupling Strategy for the Solid-1283Phase Synthesis of Tropane Derivatives" J. Org. Chem. 61, 4494-4495 (1996).

Institution fields

Peer reviewed
yes
First author
Koh
Co-authors
Koh, J. S.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Palladium-Mediated Three-Component Coupling Strategy for the Solid-Phase Synthesis of Tropane DerivativesPalladium-Mediated Three-Component Coupling Strategy for the Solid-Phase Synthesis of Tropane Derivatives1Palladium-Mediated Three-Component Coupling Strategy for the Solid-Phase Synthesis of Tropane Derivatives1
year cv 199619961996
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo960638m10.1021/jo960638m
first author openalex KohKohKoh

Citations

OpenAlex
63
Scholar
94
DOI
10.1021/jo960638m
OpenAlex
W1977593357

Match decisions

  • doi merged · 1.00 · Run 18
1996 Solid phase and combinatorial synthesis of benzodiazepines on a solid support U.S. Patent No. 5,288,514 other CV OA GS needs review

CV span

lines 1449–1450 · CV · published

144918. Ellman, J. A. “Solid phase and combinatorial synthesis of benzodiazepines on a solid support” U.S.1450(1996), Patent No. 5,288,514.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Solid phase and combinatorial synthesis of benzodiazepines on a solid support
year cv 1996
venue cv U.S. Patent No. 5,288,514
kind cv other
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

  • passthrough_guard not merged · 0.90 · year_spread · Run 18 Records correspond to the same patent for solid phase benzodiazepine synthesis.
1996 Solid phase and combinatorial synthesis of compounds on a solid support U.S. Patent No. 5,545,568 other CV OA GS

CV span

lines 1446–1447 · CV · published

144617. Ellman, J. A. “Solid phase and combinatorial synthesis of compounds on a solid support” U.S.1447(1996), Patent No. 5,545,568.

Institution fields

Peer reviewed
none
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Solid phase and combinatorial synthesis of compounds on a solid supportSolid phase and combinatorial synthesis of compounds on a solid support
year cv 19961996
venue cv U.S. Patent No. 5,545,568US Patent
kind cv otherother
first author cv EllmanEllman

Citations

OpenAlex
none
Scholar
130

Match decisions

  • fingerprint merged · 1.00 · Run 18
1996 Solid-Phase Synthesis: Application of Combinatorial Libraries Annual reports in medicinal chemistry chapter CV OA GS

CV span

lines 1268–1269 · CV · published

1268318. Choong, I. C.; Ellman, J. A. "Solid-Phase Synthesis: Application of Combinatorial Libraries" in1269Annu. Rep. Med. Chem. 31, 309-318 (1996).

Institution fields

Peer reviewed
yes
First author
Choong
Co-authors
Choong, I. C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Solid-Phase Synthesis: Application of Combinatorial LibrariesChapter 31. Solid-Phase Synthesis: Applications to Combinatorial LibrariesSolid-phase synthesis: Applications to combinatorial libraries
year cv 199619961996
venue openalex Annu. Rep. Med. Chem.Annual reports in medicinal chemistryAnnual reports in medicinal chemistry
kind cv chapterchapterother
DOI openalex 10.1016/s0065-7743(08)60470-4
first author openalex ChoongChoongChoong

Citations

OpenAlex
29
Scholar
42
DOI
10.1016/s0065-7743(08)60470-4
OpenAlex
W1542692244

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1016/s0065-7743(08)60470-4 for solid-phase synthesis book chapter.
1996 Synthesis and Applications of Small Molecule Libraries Chemical Reviews article journal CV OA GS needs review

CV span

lines 1295–1296 · CV · published

1295326. Thompson, L. A.; Ellman, J. A. "Synthesis and Applications of Small Molecule Libraries" Chem.1296Rev. 96, 555-600 (1996).

Institution fields

Peer reviewed
yes
First author
Thompson
Co-authors
Thompson, L. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Applications of Small Molecule LibrariesSynthesis and Applications of Small Molecule LibrariesSynthesis and applications of small molecule libraries
year cv 199619961996
venue crossref Chem. Rev.Chemical ReviewsChemical reviewsChemical Reviews
kind cv articlereviewother
DOI crossref 10.1021/cr940208110.1021/cr9402081
first author openalex ThompsonThompsonThompson

Citations

OpenAlex
1455
Scholar
2151
DOI
10.1021/cr9402081
OpenAlex
W2089571021

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/cr9402081 for synthesis and applications of small molecule libraries.
  • doi merged · 1.00 · Run 18
1996 Synthesis and Evaluation of 1,4-Benzodiazepine Libraries Methods in Enzymology reprint 1996 Synthesis and Evaluation of 1,4-Benzodiazepine Libraries article CV OA GS needs review

CV span

lines 1305–1306 · CV · published

1305329. Bunin, B. A.; Plunkett, M. J.; Ellman, J. A. "Synthesis and Evaluation of 1,4-Benzodiazepine1306Libraries" Methods Enzymol. 267, 448-467 (1996).

Institution fields

Peer reviewed
yes
First author
Bunin
Co-authors
Bunin, B. A.; Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Synthesis and Evaluation of 1,4-Benzodiazepine Libraries
year cv 1996
venue crossref Methods Enzymol.Methods in Enzymology
kind cv article
DOI crossref 10.1016/s0076-6879(96)67028-1
first author cv Bunin

Citations

OpenAlex
none
Scholar
none
Scholar with related records
34
DOI
10.1016/s0076-6879(96)67028-1

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1016/s0076-6879(96)67028-1 for synthesis and evaluation of 1,4-benzodiazepine libraries.
1996 The Solid-Phase Synthesis of Complex Small Molecules CHIMIA article journal CV OA GS

CV span

lines 1289–1290 · CV · published

1289324. Ellman, J. A. "The Solid-Phase Synthesis of Complex Small Molecules" Chimia 50, 260-2611290(1996).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Solid-Phase Synthesis of Complex Small MoleculesThe Solid-Phase Synthesis of Complex Small Molecules
year cv 19961996
venue crossref ChimiaCHIMIA International Journal for ChemistryCHIMIA
kind cv articlearticle
DOI crossref 10.2533/chimia.1996.26010.2533/chimia.1996.260
first author openalex EllmanEllman

Citations

OpenAlex
4
Scholar
none
DOI
10.2533/chimia.1996.260
OpenAlex
W2480814914

Match decisions

  • doi merged · 1.00 · Run 18
1995 A General and Straightforward Method for the Solid-Phase Synthesis of 1,4-Benzodiazepine-2,5-diones J. Org. Chem. article journal CV OA GS

CV span

lines 1308–1309 · CV · published

1308330. Boojamra, C G.; Burow, K. J.; Ellman, J. A. "A General and Straightforward Method for the Solid-1309Phase Synthesis of 1,4-Benzodiazepine-2,5-diones" J. Org. Chem. 60, 5742-5743 (1995).

Institution fields

Peer reviewed
yes
First author
Boojamra
Co-authors
Boojamra, C G.; Burow, K. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv A General and Straightforward Method for the Solid-Phase Synthesis of 1,4-Benzodiazepine-2,5-diones
year cv 1995
venue cv J. Org. Chem.
kind cv article
first author cv Boojamra

Citations

OpenAlex
none
Scholar
none

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jo00123a001 and matching titles for benzodiazepine-2,5-diones.
1995 An expedient and high-yielding method for the solid-phase synthesis of diverse 1,4-benzodiazepine-2,5-diones The Journal of Organic Chemistry article journal CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title openalex An expedient and high-yielding method for the solid-phase synthesis of diverse 1,4-benzodiazepine-2,5-dionesAn expedient and high-yielding method for the solid-phase synthesis of diverse 1, 4-benzodiazepine-2, 5-diones
year openalex 19951995
venue openalex The Journal of Organic ChemistryThe Journal of Organic Chemistry
kind openalex articleother
DOI openalex 10.1021/jo00123a001
first author openalex BoojamraBoojamra

Citations

OpenAlex
143
Scholar
222
DOI
10.1021/jo00123a001
OpenAlex
W2028644986

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/jo00123a001 and matching titles for benzodiazepine-2,5-diones.
1995 Combinatorial Asymmetric Catalyst Development. General Solid-Phase Synthesis Strategy for the Preparation of 2-Pyrrolidinemethanol Ligands The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1298–1300 · CV · published

1298327. Liu, G.; Ellman, J. A. "Combinatorial Asymmetric Catalyst Development. General Solid-Phase1299Synthesis Strategy for the Preparation of 2-Pyrrolidinemethanol Ligands" J. Org. Chem. 60, 7712-13007713 (1995).

Institution fields

Peer reviewed
yes
First author
Liu
Co-authors
Liu, G.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Asymmetric Catalyst Development. General Solid-Phase Synthesis Strategy for the Preparation of 2-Pyrrolidinemethanol LigandsA General Solid-Phase Synthesis Strategy for the Preparation of 2-Pyrrolidinemethanol LigandsA general solid-phase synthesis strategy for the preparation of 2-pyrrolidinemethanol ligands
year cv 199519951995
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo00129a00210.1021/jo00129a002
first author openalex LiuLiuLiu

Citations

OpenAlex
148
Scholar
234
DOI
10.1021/jo00129a002
OpenAlex
W2074666175

Match decisions

  • doi merged · 1.00 · Run 18
1995 Combinatorial Organic Libraries CHEMTRACTS: Org. Chem. article CV OA GS

CV span

lines 1315–1315 · CV · published

1315332. Ellman, J. A. "Combinatorial Organic Libraries" CHEMTRACTS: Org. Chem. 8, 1-4 (1995).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
none
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Combinatorial Organic Libraries
year cv 1995
venue cv CHEMTRACTS: Org. Chem.
kind cv article
first author cv Ellman

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1995 Expedient Method for the Solid-Phase Synthesis of Aspartic Acid Protease Inhibitors Directed toward the Generation of Libraries Journal of Medicinal Chemistry article journal CV OA GS needs review

CV span

lines 1317–1319 · CV · published

1317333. Kick, E. K.; Ellman, J. A. "Expedient Method for the Solid-Phase Synthesis of Aspartic Acid1318Protease Inhibitors Directed toward the Generation of Libraries" J. Med. Chem. 38, 1427-14301319(1995).

Institution fields

Peer reviewed
yes
First author
Kick
Co-authors
Kick, E. K.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Expedient Method for the Solid-Phase Synthesis of Aspartic Acid Protease Inhibitors Directed toward the Generation of LibrariesExpedient method for the solid-phase synthesis of aspartic acid protease inhibitors directed toward the generation of libraries
year cv 19951995
venue crossref J. Med. Chem.Journal of medicinal chemistryJournal of Medicinal Chemistry
kind cv articleother
DOI crossref 10.1021/jm00009a002
first author cv KickKick

Citations

OpenAlex
none
Scholar
213
DOI
10.1021/jm00009a002

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/jm00009a002 for aspartic acid protease inhibitors.
  • fingerprint merged · 1.00 · Run 18
1995 Photochemically-Initiated Protein Splicing Angewandte Chemie International Edition in English article journal CV OA GS

CV span

lines 1345–1346 · CV · published

1345341. Cook, S. N.; Jack, W. E.; Xiong, X.; Danley, L. E.; Ellman, J. A.; Schultz, P. G.; Noren, C. J.1346"Photochemically-Initiated Protein Splicing" Angew. Chem., Int. Ed. Engl. 34, 1629-1630 (1995).

Institution fields

Peer reviewed
yes
First author
Cook
Co-authors
Cook, S. N.; Jack, W. E.; Xiong, X.; Danley, L. E.; Ellman, J. A.; Schultz, P. G.; Noren, C. J.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Photochemically-Initiated Protein SplicingPhotochemically Initiated Protein SplicingPhotochemically initiated protein splicing
year cv 199519951995
venue crossref Angew. Chem., Int. Ed. Engl.Angewandte Chemie International Edition in EnglishAngewandte Chemie International Edition in EnglishAngewandte Chemie International Edition in English
kind cv articlearticleother
DOI crossref 10.1002/anie.19951629110.1002/anie.199516291
first author openalex CookCookCook

Citations

OpenAlex
49
Scholar
65
DOI
10.1002/anie.199516291
OpenAlex
W2161924177

Match decisions

  • doi merged · 1.00 · Run 18
1995 Silicon-Based Linkage Strategy for Traceless Solid-Phase Synthesis The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 1302–1303 · CV · published

1302328. Plunkett, M. J.; Ellman, J. A. "Silicon-Based Linkage Strategy for Traceless Solid-Phase Synthesis"1303J. Org. Chem. 60, 6006-6007 (1995).

Institution fields

Peer reviewed
yes
First author
Plunkett
Co-authors
Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Silicon-Based Linkage Strategy for Traceless Solid-Phase SynthesisA Silicon-Based Linker for Traceless Solid-Phase SynthesisA silicon-based linker for traceless solid-phase synthesis
year cv 199519951995
venue crossref J. Org. Chem.The Journal of Organic ChemistryThe Journal of Organic ChemistryThe Journal of Organic Chemistry
kind cv articlearticleother
DOI crossref 10.1021/jo00124a00510.1021/jo00124a005
first author openalex PlunkettPlunkettPlunkett

Citations

OpenAlex
205
Scholar
296
DOI
10.1021/jo00124a005
OpenAlex
W2039328214

Match decisions

  • doi merged · 1.00 · Run 18
1995 Stille Coupling in the Solid Phase Synthesis of Structurally Diverse 1,4-Benzodiazepine Derivatives Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1321–1322 · CV · published

1321334. Plunkett, M. J.; Ellman, J. A. "Stille Coupling in the Solid Phase Synthesis of Structurally Diverse13221,4-Benzodiazepine Derivatives" J. Am. Chem. Soc. 117, 3306-3307 (1995).

Institution fields

Peer reviewed
yes
First author
Plunkett
Co-authors
Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Stille Coupling in the Solid Phase Synthesis of Structurally Diverse 1,4-Benzodiazepine DerivativesSolid-Phase Synthesis of Structurally Diverse 1,4-Benzodiazepine Derivatives Using the Stille Coupling ReactionSolid-phase synthesis of structurally diverse 1, 4-benzodiazepine derivatives using the Stille coupling reaction
year cv 199519951995
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00116a04910.1021/ja00116a049
first author openalex PlunkettPlunkettPlunkett

Citations

OpenAlex
165
Scholar
230
DOI
10.1021/ja00116a049
OpenAlex
W2949579733

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja00116a049 for Stille coupling in solid phase synthesis.
  • doi merged · 1.00 · Run 18
1994 Carbon-Carbon Bond Forming Methods on Solid Support. Utilization of Kenner's "Safety-Catch" Linker Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1330–1331 · CV · published

1330337. Backes, B. J.; Ellman, J. A. "Carbon-Carbon Bond Forming Methods on Solid Support. Utilization1331of Kenner's "Safety-Catch" Linker" J. Am. Chem. Soc. 116, 11171-11172 (1994).

Institution fields

Peer reviewed
yes
First author
Backes
Co-authors
Backes, B. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Carbon-Carbon Bond Forming Methods on Solid Support. Utilization of Kenner's "Safety-Catch" LinkerCarbon-Carbon Bond-Forming Methods on Solid Support. Utilization of Kenner's "Safety-Catch" LinkerCarbon-carbon bond-forming methods on solid support. Utilization of Kenner's" safety-catch" linker
year cv 199419941994
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00103a04810.1021/ja00103a048
first author openalex BackesBackesBackes

Citations

OpenAlex
208
Scholar
275
DOI
10.1021/ja00103a048
OpenAlex
W2949643240

Match decisions

  • doi merged · 1.00 · Run 18
1994 Increasing the Diversity of a 1,4-Benzodiazepine Library through Side-Chain Functionalization Polym. Prepr. article CV OA GS

CV span

lines 1333–1334 · CV · published

1333338. Bunin, B. A.; Ellman, J. A. "Increasing the Diversity of a 1,4-Benzodiazepine Library through1334Side-Chain Functionalization" Polym. Prepr. 35, 983, (1994).

Institution fields

Peer reviewed
yes
First author
Bunin
Co-authors
Bunin, B. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Increasing the Diversity of a 1,4-Benzodiazepine Library through Side-Chain Functionalization
year cv 1994
venue cv Polym. Prepr.
kind cv article
first author cv Bunin

Citations

OpenAlex
none
Scholar
none

Match decisions

No decision recorded; a single record.

1994 Simultaneous Solid-Phase Synthesis of -Turn Mimetics Incorporating Side-chain Functionality Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1327–1328 · CV · published

1327336. Virgilio, A. A.; Ellman, J. A. "Simultaneous Solid-Phase Synthesis of -Turn Mimetics1328Incorporating Side-chain Functionality" J. Am. Chem. Soc. 116, 11580-11581 (1994).

Institution fields

Peer reviewed
yes
First author
Virgilio
Co-authors
Virgilio, A. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Simultaneous Solid-Phase Synthesis of -Turn Mimetics Incorporating Side-chain FunctionalitySimultaneous Solid-Phase Synthesis of .beta.-Turn Mimetics Incorporating Side-Chain FunctionalitySimultaneous Solid-Phase Synthesis of. beta.-Turn Mimetics Incorporating Side-Chain Functionality
year cv 199419941994
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00104a05310.1021/ja00104a053
first author openalex VirgilioVirgilioVirgilio

Citations

OpenAlex
133
Scholar
211
DOI
10.1021/ja00104a053
OpenAlex
W2949655188

Match decisions

  • doi merged · 1.00 · Run 18
1994 Solid phase and combinatorial synthesis of benzodiazepine compounds on a solid support US Patent 5,288 other CV OA GS Scholar only needs review

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title scholar Solid phase and combinatorial synthesis of benzodiazepine compounds on a solid support
year scholar 1994
venue scholar US Patent
kind scholar other
first author scholar Ellman

Citations

OpenAlex
none
Scholar
1058

Match decisions

  • passthrough_guard not merged · 0.90 · year_spread · Run 18 Records correspond to the same patent for solid phase benzodiazepine synthesis.
1994 Straightforward and General Method for Coupling Alcohols to Solid-Supports Tetrahedron Letters article journal CV OA GS

CV span

lines 1324–1325 · CV · published

1324335. Thompson, L. A.; Ellman, J. A. "Straightforward and General Method for Coupling Alcohols to1325Solid-Supports" Tetrahedron Lett. 35, 9333-9336 (1994).

Institution fields

Peer reviewed
yes
First author
Thompson
Co-authors
Thompson, L. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Straightforward and General Method for Coupling Alcohols to Solid-SupportsStraightforward and general method for coupling alcohols to solid supportsStraightforward and general method for coupling alcohols to solid supports
year cv 199419941994
venue crossref Tetrahedron Lett.Tetrahedron LettersTetrahedron lettersTetrahedron Letters
kind cv articlearticleother
DOI crossref 10.1016/s0040-4039(00)78535-210.1016/s0040-4039(00)78535-2
first author openalex ThompsonThompsonThompson

Citations

OpenAlex
190
Scholar
284
DOI
10.1016/s0040-4039(00)78535-2
OpenAlex
W2162303607

Match decisions

  • doi merged · 1.00 · Run 18
1994 The Combinatorial Synthesis, and Chemical and Biological Evaluation of a 1,4-Benzodiazepine Library Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 1336–1338 · CV · published

1336339. Bunin, B. A.; Plunkett, M. J.; Ellman, J. A. "The Combinatorial Synthesis, and Chemical and1337Biological Evaluation of a 1,4-Benzodiazepine Library" Proc. Natl. Acad. Sci USA, 91, 4708-47121338(1994).

Institution fields

Peer reviewed
yes
First author
Bunin
Co-authors
Bunin, B. A.; Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Combinatorial Synthesis, and Chemical and Biological Evaluation of a 1,4-Benzodiazepine LibraryThe combinatorial synthesis and chemical and biological evaluation of a 1,4-benzodiazepine library.The combinatorial synthesis and chemical and biological evaluation of a 1, 4-benzodiazepine library.
year cv 199419941994
venue crossref Proc. Natl. Acad. Sci USAProceedings of the National Academy of SciencesProceedings of the National Academy of SciencesProceedings of the National Academy of Sciences
kind cv articlearticleother
DOI crossref 10.1073/pnas.91.11.470810.1073/pnas.91.11.4708
first author openalex BuninBuninBunin

Citations

OpenAlex
260
Scholar
462
DOI
10.1073/pnas.91.11.4708
OpenAlex
W1983646492

Match decisions

  • doi merged · 1.00 · Run 18
1993 Protein Biosynthesis with Conformationally Restricted Amino Acids Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1348–1349 · CV · published

1348342. Mendel, D.; Ellman, J.; Schultz, P. G. "Protein Biosynthesis with Conformationally Restricted1349Amino Acids" J. Am. Chem. Soc. 115, 4359-4360 (1993).

Institution fields

Peer reviewed
yes
First author
Mendel
Co-authors
Mendel, D.; Ellman, J.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Protein Biosynthesis with Conformationally Restricted Amino AcidsProtein biosynthesis with conformationally restricted amino acidsProtein biosynthesis with conformationally restricted amino acids
year cv 199319931993
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00063a06310.1021/ja00063a063
first author openalex MendelMendelMendel

Citations

OpenAlex
84
Scholar
114
DOI
10.1021/ja00063a063
OpenAlex
W2094335437

Match decisions

  • doi merged · 1.00 · Run 18
1992 General and Expedient Method for the Solid-Phase Synthesis of 1,4-Benzodiazepine Derivatives Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1340–1343 · CV · published

1340340. Bunin, B. A.; Ellman, J. A. “General and Expedient Method for the Solid-Phase Synthesis of 1,4-1341Benzodiazepine Derivatives" J. Am. Chem. Soc. 114, 10997-10998 (1992). Commentaries on the1342publication were reported in both Chemical and Engineering News 71, 33-34 (1993) and in the New1343Scientist 137, 14 (1993).

Institution fields

Peer reviewed
yes
First author
Bunin
Co-authors
Bunin, B. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv General and Expedient Method for the Solid-Phase Synthesis of 1,4-Benzodiazepine DerivativesA general and expedient method for the solid-phase synthesis of 1,4-benzodiazepine derivativesA general and expedient method for the solid-phase synthesis of 1, 4-benzodiazepine derivatives
year cv 199219921992
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00053a06710.1021/ja00053a067
first author openalex BuninBuninBunin

Citations

OpenAlex
443
Scholar
756
DOI
10.1021/ja00053a067
OpenAlex
W2028983179

Match decisions

  • doi merged · 1.00 · Run 18
1992 Probing Protein Stability with Unnatural Amino Acids Science article journal CV OA GS

CV span

lines 1354–1355 · CV · published

1354344. Mendel, D.; Ellman, J. A.; Chang, Z.; Veenstra, D. L.; Kollman, P. A.; Schultz, P. G. "Probing1355Protein Stability with Unnatural Amino Acids" Science 256, 1798-1802 (1992).

Institution fields

Peer reviewed
yes
First author
Mendel
Co-authors
Mendel, D.; Ellman, J. A.; Chang, Z.; Veenstra, D. L.; Kollman, P. A.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Probing Protein Stability with Unnatural Amino AcidsProbing Protein Stability with Unnatural Amino AcidsProbing protein stability with unnatural amino acids
year cv 199219921992
venue crossref ScienceScienceScience
kind cv articlearticleother
DOI crossref 10.1126/science.161532410.1126/science.1615324
first author openalex MendelMendelMendel

Citations

OpenAlex
158
Scholar
205
DOI
10.1126/science.1615324
OpenAlex
W1992824521

Match decisions

  • doi merged · 1.00 · Run 18
1992 Site-Specific Incorporation of Novel Backbone Structures into Proteins Science article journal CV OA GS

CV span

lines 1357–1359 · CV · published

1357345. Ellman, J. A.; Mendel, D. Schultz, P. G. "Site-Specific Incorporation of Novel Backbone Structures1358into Proteins" Science 255, 197-200 (1992).1359

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J. A.; Mendel, D.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Site-Specific Incorporation of Novel Backbone Structures into ProteinsSite-Specific Incorporation of Novel Backbone Structures into ProteinsSite-specific incorporation of novel backbone structures into proteins
year cv 199219921992
venue crossref ScienceScienceScience
kind cv articlearticleother
DOI crossref 10.1126/science.155354610.1126/science.1553546
first author openalex EllmanEllmanEllman

Citations

OpenAlex
190
Scholar
389
DOI
10.1126/science.1553546
OpenAlex
W1969303801

Match decisions

  • doi merged · 1.00 · Run 18
1992 Site-Specific Isotopic Labeling of Proteins for NMR Studies Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1351–1352 · CV · published

1351343. Ellman, J. A.; Volkman, B. F.; Mendel, D.; Schultz, P. G.; Wemmer, D. E. "Site-Specific Isotopic1352Labeling of Proteins for NMR Studies"J. Am. Chem. Soc. 114, 7959-7961 (1992).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J. A.; Volkman, B. F.; Mendel, D.; Schultz, P. G.; Wemmer, D. E.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Site-Specific Isotopic Labeling of Proteins for NMR StudiesSite-specific isotopic labeling of proteins for NMR studiesSite-specific isotopic labeling of proteins for NMR studies
year cv 199219921992
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00046a08010.1021/ja00046a080
first author openalex EllmanEllmanEllman

Citations

OpenAlex
74
Scholar
85
DOI
10.1021/ja00046a080
OpenAlex
W2010456755

Match decisions

  • doi merged · 1.00 · Run 18
1991 A Biosynthetic Method for Introducing Unnatural Amino Acids Site-Specifically into Proteins Methods in Enzymology article CV OA GS

CV span

lines 1360–1362 · CV · published

1360346. Ellman, J.; Mendel, D.; Noren, C. J.; Anthony-Cahill, S. J.; Schultz, P. G. "A Biosynthetic Method1361for Introducing Unnatural Amino Acids Site-Specifically into Proteins" Methods Enzymol. 202,1362301-336 (1991).

Institution fields

Peer reviewed
yes
First author
Ellman
Co-authors
Ellman, J.; Mendel, D.; Noren, C. J.; Anthony-Cahill, S. J.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A Biosynthetic Method for Introducing Unnatural Amino Acids Site-Specifically into Proteins[15] Biosynthetic method for introducing unnatural amino acids site-specifically into proteins
year cv 19911991
venue crossref Methods Enzymol.Methods in enzymologyMethods in Enzymology
kind cv articleother
DOI crossref 10.1016/0076-6879(91)02017-4
first author cv EllmanEllman

Citations

OpenAlex
none
Scholar
524
DOI
10.1016/0076-6879(91)02017-4

Match decisions

  • fingerprint merged · 1.00 · Run 18
1991 A General and Efficient Route for Chemical Aminoacylation of Transfer RNAs Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1367–1368 · CV · published

1367348. Robertson, S. A.; Ellman, J. A.; Schultz, P. G. "A General and Efficient Route for Chemical1368Aminoacylation of Transfer RNAs" J. Am. Chem. Soc. 113, 2722-2729 (1991).

Institution fields

Peer reviewed
yes
First author
Robertson
Co-authors
Robertson, S. A.; Ellman, J. A.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv A General and Efficient Route for Chemical Aminoacylation of Transfer RNAsA general and efficient route for chemical aminoacylation of transfer RNAsA general and efficient route for chemical aminoacylation of transfer RNAs
year cv 199119911991
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00007a05510.1021/ja00007a055
first author openalex RobertsonRobertsonRobertson

Citations

OpenAlex
213
Scholar
321
DOI
10.1021/ja00007a055
OpenAlex
W2029445449

Match decisions

  • doi merged · 1.00 · Run 18
1991 Construction of a Caged Protein by Site-Specific Unnatural Amino Acid Mutagenesis Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1364–1365 · CV · published

1364347. Mendel, D.; Ellman J. A.; Schultz, P. G. "Construction of a Caged Protein by Site-Specific1365Unnatural Amino Acid Mutagenesis" J. Am. Chem. Soc. 113, 2758-2760 (1991).

Institution fields

Peer reviewed
yes
First author
Mendel
Co-authors
Mendel, D.; Ellman J. A.; Schultz, P. G.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholar
title cv Construction of a Caged Protein by Site-Specific Unnatural Amino Acid MutagenesisConstruction of a light-activated protein by unnatural amino acid mutagenesisConstruction of a light-activated protein by unnatural amino acid mutagenesis
year cv 199119911991
venue openalex J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI openalex 10.1021/ja00007a063
first author openalex MendelMendelMendel

Citations

OpenAlex
124
Scholar
172
DOI
10.1021/ja00007a063
OpenAlex
W2005547417

Match decisions

  • gemini merged · 0.90 · Run 18 Records describe the construction of caged proteins by site-specific unnatural amino acid mutagenesis.
1990 The Asymmetric Synthesis of -Amino Acids. Electrophilic Azidation of Chiral Imide Enolates, a Practical Approach to the Synthesis of (R)- and (S)--Azido Carboxylic Acids Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1370–1373 · CV · published

1370349. Evans, D. A.; Britton, T. C.; Ellman, J. A.; Dorow, R. L. "The Asymmetric Synthesis of -Amino1371Acids. Electrophilic Azidation of Chiral Imide Enolates, a Practical Approach to the Synthesis of1372(R)- and (S)--Azido Carboxylic Acids" J. Am. Chem. Soc. 112, 4011-4030 (1990).1373

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A.; Britton, T. C.; Ellman, J. A.; Dorow, R. L.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Asymmetric Synthesis of -Amino Acids. Electrophilic Azidation of Chiral Imide Enolates, a Practical Approach to the Synthesis of (R)- and (S)--Azido Carboxylic AcidsThe asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acidsThe asymmetric synthesis of. alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)-and (S)-. alpha.-azido …
year cv 199019901990
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00166a04510.1021/ja00166a045
first author openalex EvansEvansEvans

Citations

OpenAlex
451
Scholar
693
DOI
10.1021/ja00166a045
OpenAlex
W2022589966

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/ja00166a045 for asymmetric synthesis of alpha-amino acids.
1989 The Oxidative Macrocyclization of Phenolic Peptides. A Biomimetic Approach to the Synthesis of the Vancomycin Family of Antibiotics Journal of the American Chemical Society article journal CV OA GS

CV span

lines 1374–1376 · CV · published

1374350. Evans, D. A.; Ellman, J. A.; DeVries, K. M. "The Oxidative Macrocyclization of Phenolic Peptides.1375A Biomimetic Approach to the Synthesis of the Vancomycin Family of Antibiotics" J. Am. Chem.1376Soc. 111, 8912-8914 (1989).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A.; Ellman, J. A.; DeVries, K. M.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Oxidative Macrocyclization of Phenolic Peptides. A Biomimetic Approach to the Synthesis of the Vancomycin Family of AntibioticsThe oxidative macrocyclization of phenolic peptides. A biomimetic approach to the synthesis of the vancomycin family of antibioticsThe oxidative macrocyclization of phenolic peptides. A biomimetic approach to the synthesis of the vancomycin family of antibiotics
year cv 198919891989
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00206a02110.1021/ja00206a021
first author openalex EvansEvansEvans

Citations

OpenAlex
95
Scholar
131
DOI
10.1021/ja00206a021
OpenAlex
W1984465366

Match decisions

  • doi merged · 1.00 · Run 18
1989 The Total Synthesis of the Isodityrosine-Derived Cyclic Tripeptides OF4949-III and K-13. Determination of the Absolute Configuration of K-13 Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 1378–1380 · CV · published

1378351. Evans, D. A.; Ellman, J. A. "The Total Synthesis of the Isodityrosine-Derived Cyclic Tripeptides1379OF4949-III and K-13. Determination of the Absolute Configuration of K-13" J. Am. Chem. Soc.1380111, 1063-1072 (1989).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv The Total Synthesis of the Isodityrosine-Derived Cyclic Tripeptides OF4949-III and K-13. Determination of the Absolute Configuration of K-13The total syntheses of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13. Determination of the absolute configuration of K-13The total syntheses of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13. Determination of the absolute configuration of K-13
year cv 198919891989
venue crossref J. Am. Chem. Soc.Journal of the American Chemical SocietyJournal of the American Chemical SocietyJournal of the American Chemical Society
kind cv articlearticleother
DOI crossref 10.1021/ja00185a04210.1021/ja00185a042
first author openalex EvansEvansEvans

Citations

OpenAlex
145
Scholar
225
DOI
10.1021/ja00185a042
OpenAlex
W1978640043

Match decisions

  • passthrough_guard not merged · 1.00 · doi_conflict · Run 18 Records share the DOI 10.1021/ja00185a042 for total synthesis of cyclic tripeptides OF4949-III and K-13.
  • doi merged · 1.00 · Run 18
1988 Asymmetric Synthesis of Amino Acids Peptides chapter journal CV OA GS

CV span

lines 1389–1391 · CV · published

1389354. Evans, D. A.; Weber, A. E.; Britton, T. C.; Ellman, J. A.; Sjogren, E. B. "Asymmetric Synthesis of1390Amino Acids" in Peptides: Chemistry And Biology; Tenth American Peptide Symposium; Marshall,1391G. R. (Ed.); Escom Science Publishers B.V.: Leiden, Netherlands. Illus. 143-148 (1988).

Institution fields

Peer reviewed
none
First author
Evans
Co-authors
Evans, D. A.; Weber, A. E.; Britton, T. C.; Ellman, J. A.; Sjogren, E. B.
Subfield
other
Method
none
Invited
none
Publisher
Escom Science Publishers B.V.
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Synthesis of Amino AcidsAsymmetric synthesis of amino acids
year cv 19881988
venue crossref Peptides: Chemistry And Biology; Tenth American Peptide SymposiumPeptidesPeptides
kind cv chapterchapter
DOI crossref 10.1007/978-94-010-9595-2_4210.1007/978-94-010-9595-2_42
first author openalex EvansEvans

Citations

OpenAlex
7
Scholar
none
DOI
10.1007/978-94-010-9595-2_42
OpenAlex
W2498013172

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the DOI 10.1021/ja00166a045 for asymmetric synthesis of alpha-amino acids.
1987 Asymmetric Halogenation of Chiral Imide Enolates. A General Approach to the Synthesis of Enantiomerically Pure -Amino Acids Tetrahedron Letters article journal CV OA GS

CV span

lines 1382–1384 · CV · published

1382352. Evans, D. A.; Ellman, J. A.; Dorow, R. L. "Asymmetric Halogenation of Chiral Imide Enolates. A1383General Approach to the Synthesis of Enantiomerically Pure -Amino Acids" Tetrahedron Lett. 28,13841123-1126 (1987).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A.; Ellman, J. A.; Dorow, R. L.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Asymmetric Halogenation of Chiral Imide Enolates. A General Approach to the Synthesis of Enantiomerically Pure -Amino AcidsAsymmetric halogenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure α-amino acids.
year cv 19871987
venue crossref Tetrahedron Lett.Tetrahedron lettersTetrahedron Letters
kind cv articleother
DOI crossref 10.1016/s0040-4039(00)95305-x
first author cv EvansEvans

Citations

OpenAlex
none
Scholar
219
DOI
10.1016/s0040-4039(00)95305-x

Match decisions

  • fingerprint merged · 1.00 · Run 18
1987 Contrasteric Carboximide Hydrolysis with Lithium Hydroperoxide Tetrahedron Letters article journal CV OA GS

CV span

lines 1386–1387 · CV · published

1386353. Evans, D. A; Britton, T. C.; Ellman, J. A. "Contrasteric Carboximide Hydrolysis with Lithium1387Hydroperoxide" Tetrahedron Lett. 28, 6141-6144 (1987).

Institution fields

Peer reviewed
yes
First author
Evans
Co-authors
Evans, D. A; Britton, T. C.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Contrasteric Carboximide Hydrolysis with Lithium HydroperoxideContrasteric carboximide hydrolysis with lithium hydroperoxide
year cv 19871987
venue crossref Tetrahedron Lett.Tetrahedron LettersTetrahedron Letters
kind cv articleother
DOI crossref 10.1016/s0040-4039(00)61830-0
first author cv EvansEvans

Citations

OpenAlex
none
Scholar
766
DOI
10.1016/s0040-4039(00)61830-0

Match decisions

  • fingerprint merged · 1.00 · Run 18
Anthony-Cahill, S., Noren, CJ, & Schultz, PG (1991) Methods in Enzymology article CV OA GS Scholar only

CV span

Not in the CV.

Fields by source

FieldCVOpenAlexScholar
title scholar Anthony-Cahill, S., Noren, CJ, & Schultz, PG (1991)
venue scholar Methods in Enzymology
kind scholar other
first author scholar Ellman

Citations

OpenAlex
none
Scholar
27

Match decisions

No decision recorded; a single record.

Not counted

1 item · dissertations, talks, media, datasets · listed, not counted as publications

1997 Combinatorial Chemistry and New Drugs Scientific American media not counted journal CV OA GS

CV span

lines 1258–1259 · CV · published

1258315. Plunkett, M. J.; Ellman, J. A. "Combinatorial Chemistry and New Drugs" Sci. Am. 276, 68-731259(1997).

Institution fields

Peer reviewed
no
First author
Plunkett
Co-authors
Plunkett, M. J.; Ellman, J. A.
Subfield
other
Method
none
Invited
none
Publisher
none
Reprint or translation
none

Fields by source

FieldCVOpenAlexScholarCrossRef
title cv Combinatorial Chemistry and New DrugsCombinatorial Chemistry and New DrugsCombinatorial chemistry and new drugs
year cv 199719971997
venue crossref Sci. Am.Scientific AmericanScientific AmericanScientific American
kind cv mediaarticleother
DOI crossref 10.1038/scientificamerican0497-6810.1038/scientificamerican0497-68
first author openalex PlunkettPlunkettPlunkett

Citations

OpenAlex
115
Scholar
154
DOI
10.1038/scientificamerican0497-68
OpenAlex
W2013175825

Match decisions

  • gemini merged · 1.00 · Run 18 Records share the exact DOI 10.1073/pnas.94.7.2779 and title for combinatorial thinking in chemistry and biology.

Positions

8 from the CV · current position answer · Scholar affiliation

TitleOrganizationYearsRankSourceLines
Eugene Higgins Professor of Chemistry current Yale University 2010– Distinguished named CV 3
Professor of Pharmacology current Yale University 2010– Full CV 4
Professor of Cellular and Molecular Pharmacology UC San Francisco 1999–2010 Full CV 5
Professor of Chemistry UC Berkeley 1999–2010 Full CV 6
Associate Professor of Chemistry UC Berkeley 1997–1998 Associate CV 7
Assistant Professor of Chemistry UC Berkeley 1992–1997 Assistant CV 8
National Science Foundation Postdoctoral Fellow 1989–1992 Postdoc CV 12
Joel H. Hildebrand Associate Professor Chair in Chemistry 1996–1998 Associate named CV 38
Eugene Higgins Professor of Chemistry Distinguished named CV current position 3
Yale Unknown Scholar

Entries needing review

0

Nothing to review.

Entries dropped by a reviewer

0

No dropped entries.