Tomislav Rovis

2019 Asymmetric d-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 667–669 · CV · published

667“Asymmetric d-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme.” I. S. Hassan, A. N. Ta, M. W.668Danneman, N. Semakul, M. Burns, C. H. Basch, V. N. Dippon, B. R. McNaughton*, T. Rovis*. J. Am. Chem. Soc. 2019,669141, 4815-4819.

Institution fields

Peer reviewed: yes
First author: Hassan
Co-authors: I. S. Hassan; A. N. Ta; M. W. Danneman; N. Semakul; M. Burns; C. H. Basch; V. N. Dippon; B. R. McNaughton*; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric d-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme.	Asymmetric δ-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme
year cv	2019	2019
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.9b01596	10.1021/jacs.9b01596
first author openalex	Hassan	Hassan

Citations

OpenAlex: 132
Scholar: none
DOI: 10.1021/jacs.9b01596
OpenAlex: W2922256660

Match decisions

doi merged · 1.00 · Run 18

2019 Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins Journal of the American Chemical Society article journal CV OA GS

CV span

lines 658–659 · CV · published

658“Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins” H. Lei and T. Rovis*. J.659Am. Chem. Soc. 2019, 141, 2268-2273.

Institution fields

Peer reviewed: yes
First author: Lei
Co-authors: H. Lei; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins	Ir-Catalyzed Intermolecular Branch-Selective Allylic C–H Amidation of Unactivated Terminal Olefins
year cv	2019	2019
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.9b00237	10.1021/jacs.9b00237
first author openalex	Lei	Lei

Citations

OpenAlex: 199
Scholar: none
DOI: 10.1021/jacs.9b00237
OpenAlex: W2911325032

Match decisions

doi merged · 1.00 · Run 18

2019 Photoinduced Ligand-to-Metal Charge Transfer Enables Photocatalyst-Independent Light-Gated Activation of Co(II). ACS Catalysis article journal CV OA GS

CV span

lines 652–653 · CV · published

652“Photoinduced Ligand-to-Metal Charge Transfer Enables Photocatalyst-Independent Light-Gated Activation of Co(II).” B. D.653Ravetz, J. Y. Wang, K. E. Ruhl, T. Rovis*. ACS Catal. 2019, 9, 200-204.

Institution fields

Peer reviewed: yes
First author: Ravetz
Co-authors: B. D. Ravetz; J. Y. Wang; K. E. Ruhl; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Photoinduced Ligand-to-Metal Charge Transfer Enables Photocatalyst-Independent Light-Gated Activation of Co(II).	Photoinduced Ligand-to-Metal Charge Transfer Enables Photocatalyst-Independent Light-Gated Activation of Co(II)
year cv	2019	2018
venue crossref	ACS Catal.	ACS Catalysis	ACS Catalysis
kind cv	article	article
DOI crossref	10.1021/acscatal.8b04326	10.1021/acscatal.8b04326
first author openalex	Ravetz	Ravetz

Citations

OpenAlex: 70
Scholar: none
DOI: 10.1021/acscatal.8b04326
OpenAlex: W2903879917

Match decisions

doi merged · 1.00 · Run 18

2019 Photoredox catalysis using infrared light via triplet fusion upconversion. Nature article journal CV OA GS

CV span

lines 655–656 · CV · published

655“Photoredox catalysis using infrared light via triplet fusion upconversion.” B. D. Ravetz, A. B. Pun, E. M. Churchill, D. N.656Congreve*, T. Rovis*, L. M. Campos*. Nature 2019, 565, 343-346.

Institution fields

Peer reviewed: yes
First author: Ravetz
Co-authors: B. D. Ravetz; A. B. Pun; E. M. Churchill; D. N. Congreve*; T. Rovis*; L. M. Campos*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Photoredox catalysis using infrared light via triplet fusion upconversion.	Photoredox catalysis using infrared light via triplet fusion upconversion
year cv	2019	2019
venue crossref	Nature	Nature
kind cv	article	article
DOI crossref	10.1038/s41586-018-0835-2	10.1038/s41586-018-0835-2
first author openalex	Ravetz	Ravetz

Citations

OpenAlex: 696
Scholar: 749
DOI: 10.1038/s41586-018-0835-2
OpenAlex: W2910387602

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: excluded

2019 Photoredox-Catalyzed Alkenylation of Benzylsulfoniums. Chemistry – An Asian Journal article journal CV OA GS

CV span

lines 661–663 · CV · published

661“Photoredox-Catalyzed Alkenylation of Benzylsulfoniums.” S. Otsuka, K. Nogi, T. Rovis, H. Yorimitsu*. Chem. Asian J. 2019,66214, 532-536.663

Institution fields

Peer reviewed: yes
First author: Otsuka
Co-authors: S. Otsuka; K. Nogi; T. Rovis; H. Yorimitsu*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Photoredox-Catalyzed Alkenylation of Benzylsulfoniums.	Photoredox‐Catalyzed Alkenylation of Benzylsulfonium Salts
year cv	2019	2019
venue crossref	Chem. Asian J.	Chemistry - An Asian Journal	Chemistry – An Asian Journal
kind cv	article	article
DOI crossref	10.1002/asia.201801732	10.1002/asia.201801732
first author openalex	Otsuka	Otsuka

Citations

OpenAlex: 36
Scholar: none
DOI: 10.1002/asia.201801732
OpenAlex: W2910859807

Match decisions

doi merged · 1.00 · Run 18

2019 Photoredox-Catalyzed Site-Selective a-C(sp3)-H Alkylation of Primary Amine Derivatives. Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 664–665 · CV · published

664“Photoredox-Catalyzed Site-Selective a-C(sp3)-H Alkylation of Primary Amine Derivatives.” M. A. Ashley, C. Yamauchi, J. C.665K. Chu, S. Otsuka, H. Yorimitsu, T. Rovis*. Angew. Chem. Int. Ed. 2019, 58, 4002-4006.

Institution fields

Peer reviewed: yes
First author: Ashley
Co-authors: M. A. Ashley; C. Yamauchi; J. C. K. Chu; S. Otsuka; H. Yorimitsu; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Photoredox-Catalyzed Site-Selective a-C(sp3)-H Alkylation of Primary Amine Derivatives.	Photoredox‐Catalyzed Site‐Selective α‐C(sp3)−H Alkylation of Primary Amine DerivativesPhotoredox‐Catalyzed Site‐Selective α‐C(sp3)−H Alkylation of Primary Amine Derivatives
year cv	2019	20192019
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201812227	10.1002/anie.20181222710.1002/ange.201812227
first author openalex	Ashley	AshleyAshley

Also recorded as

W4246144826 (DOI 10.1002/ange.201812227) · same title · 2019 Photoredox‐Catalyzed Site‐Selective α‐C(sp3)−H Alkylation of Primary Amine Derivatives

Citations

OpenAlex: 149
Scholar: none
DOI: 10.1002/anie.201812227
OpenAlex: W2913204808

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2019 Proton-Coupled Electron Transfer. Photocatalysis in Organic Synthesis chapter CV OA GS

CV span

lines 638–639 · CV · published

638“Proton-Coupled Electron Transfer.” S. M. Thullen, M. A. Ashley, T. Rovis*. In Science of Synthesis: Photocatalysis in Organic639Synthesis, Georg Thieme Verlag, Stuttgart. 2019, 219-242.

Institution fields

Peer reviewed: none
First author: Thullen
Co-authors: S. M. Thullen; M. A. Ashley; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: Georg Thieme Verlag, Stuttgart
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Proton-Coupled Electron Transfer.	6 Proton-Coupled Electron Transfer
year cv	2019	2019
venue crossref	Science of Synthesis: Photocatalysis in Organic Synthesis	Haug Verlag in Georg Thieme Verlag KG eBooks	Photocatalysis in Organic Synthesis
kind cv	chapter	chapter
DOI crossref	10.1055/sos-sd-229-00118	10.1055/sos-sd-229-00118
first author openalex	Thullen	Thullen

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1055/sos-sd-229-00118
OpenAlex: W3200717253

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1055/sos-sd-229-00118 for the book chapter on proton-coupled electron transfer.

2019 Rh(III)-Catalyzed C-H Activation Initiated Cyclopropanation of Allylic Alcohols. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 671–672 · CV · published

671“Rh(III)-Catalyzed C-H Activation Initiated Cyclopropanation of Allylic Alcohols.” E. J. T. Phipps and T. Rovis*. J. Am. Chem.672Soc. 2019, 141, 6807-6811.

Institution fields

Peer reviewed: yes
First author: Phipps
Co-authors: E. J. T. Phipps; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(III)-Catalyzed C-H Activation Initiated Cyclopropanation of Allylic Alcohols.	Rh(III)-Catalyzed C–H Activation-Initiated Directed Cyclopropanation of Allylic Alcohols
year cv	2019	2019
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.9b02156	10.1021/jacs.9b02156
first author openalex	Phipps	Phipps

Citations

OpenAlex: 63
Scholar: none
DOI: 10.1021/jacs.9b02156
OpenAlex: W2936999937

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1021/jacs.9b02156 for the cyclopropanation of allylic alcohols.

2019 Sterically and Electronically Tuned Cp Ligands for Rhodium(III)-Catalyzed Carbon-Hydrogen Bond Functionalization. Rhodium Catalysis in Organic Synthesis chapter CV OA GS

CV span

lines 641–642 · CV · published

641“Sterically and Electronically Tuned Cp Ligands for Rhodium(III)-Catalyzed Carbon-Hydrogen Bond Functionalization.” F.642Romanov-Michailidis, E. J. T. Phipps, T. Rovis*. In Modern Rhodium Catalyzed Reactions, editor K. Tanaka; Wiley, 2019.

Institution fields

Peer reviewed: none
First author: Romanov-Michailidis
Co-authors: F. Romanov-Michailidis; E. J. T. Phipps; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: Wiley
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Sterically and Electronically Tuned Cp Ligands for Rhodium(III)-Catalyzed Carbon-Hydrogen Bond Functionalization.	Sterically and Electronically Tuned Cp Ligands for Rhodium (III) ‐Catalyzed Carbon–Hydrogen Bond Functionalization
year cv	2019	2019
venue crossref	Modern Rhodium Catalyzed Reactions		Rhodium Catalysis in Organic Synthesis
kind cv	chapter	other
DOI crossref	10.1002/9783527811908.ch20	10.1002/9783527811908.ch20
first author openalex	Romanov-Michailidis	Romanov‐Michailidis

Citations

OpenAlex: 9
Scholar: none
DOI: 10.1002/9783527811908.ch20
OpenAlex: W2909398480

Match decisions

doi merged · 1.00 · Run 18

2019 Visible Light Controlled Ruthenium-Catalyzed Olefin Metathesis. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 674–675 · CV · published

674“Visible Light Controlled Ruthenium-Catalyzed Olefin Metathesis.” C. Theunissen, M. A. Ashley, T. Rovis*. J. Am. Chem. Soc.6752019, 141, 6791-6796.

Institution fields

Peer reviewed: yes
First author: Theunissen
Co-authors: C. Theunissen; M. A. Ashley; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Visible Light Controlled Ruthenium-Catalyzed Olefin Metathesis.	Visible-Light-Controlled Ruthenium-Catalyzed Olefin Metathesis
year cv	2019	2019
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.8b13663	10.1021/jacs.8b13663
first author openalex	Theunissen	Theunissen

Citations

OpenAlex: 100
Scholar: none
DOI: 10.1021/jacs.8b13663
OpenAlex: W2942191047

Match decisions

doi merged · 1.00 · Run 18

2018 Complementary Strategies for Directed C(sp3)−H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer Angewandte Chemie International Edition review journal CV OA GS

CV span

lines 619–621 · CV · published

619"Complementary Strategies for Directed C(sp3)−H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation,620Hydrogen Atom Transfer, and Carbene/Nitrene Transfer”. J. C.-K. Chu and T. Rovis*. Angew. Chem. Int. Ed. 2018, 57, 62-621101.

Institution fields

Peer reviewed: yes
First author: Chu
Co-authors: J. C.-K. Chu; T. Rovis*
Subfield: other
Method: review
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Complementary Strategies for Directed C(sp3)−H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer	Complementary Strategies for Directed C(sp 3 )−H Functionalization: A Comparison of Transition‐Metal‐Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer
year cv	2018	2017
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International Edition	Angewandte Chemie International Edition
kind cv	review	article
DOI crossref	10.1002/anie.201703743	10.1002/anie.201703743
first author openalex	Chu	Chu

Citations

OpenAlex: 665
Scholar: none
DOI: 10.1002/anie.201703743
OpenAlex: W2774819994

Match decisions

doi merged · 1.00 · Run 18

2018 Direct a-Alkylation of Primary Aliphatic Amines Enabled by CO2 and Electrostatics. Nature Chemistry article journal CV OA GS

CV span

lines 635–636 · CV · published

635“Direct a-Alkylation of Primary Aliphatic Amines Enabled by CO2 and Electrostatics.” J. Ye, I. Kalvet, F. Schoenebeck* and T.636Rovis.* Nature Chem. 2018, 10, 1037-1041.

Institution fields

Peer reviewed: yes
First author: Ye
Co-authors: J. Ye; I. Kalvet; F. Schoenebeck*; T. Rovis.*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Direct a-Alkylation of Primary Aliphatic Amines Enabled by CO2 and Electrostatics.	Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics
year cv	2018	2018
venue crossref	Nature Chem.	Nature Chemistry	Nature Chemistry
kind cv	article	article
DOI crossref	10.1038/s41557-018-0085-9	10.1038/s41557-018-0085-9
first author openalex	Ye	Ye

Citations

OpenAlex: 229
Scholar: none
DOI: 10.1038/s41557-018-0085-9
OpenAlex: W2884008534

Match decisions

doi merged · 1.00 · Run 18

2018 Electronic and Steric Tuning of a Prototypical Piano Stool Complex: Rhodium (III) Catalysis for C-H Functionalization. Accounts of Chemical Research article journal CV OA GS

CV span

lines 616–617 · CV · published

616"Electronic and Steric Tuning of a Prototypical Piano Stool Complex: Rhodium (III) Catalysis for C-H Functionalization." T.617Piou and T. Rovis*. Acc. Chem. Res. 2018, 51, 170-180.

Institution fields

Peer reviewed: yes
First author: Piou
Co-authors: T. Piou; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Electronic and Steric Tuning of a Prototypical Piano Stool Complex: Rhodium (III) Catalysis for C-H Functionalization.	Electronic and Steric Tuning of a Prototypical Piano Stool Complex: Rh(III) Catalysis for C–H Functionalization
year cv	2018	2017
venue crossref	Acc. Chem. Res.	Accounts of Chemical Research	Accounts of Chemical Research
kind cv	article	article
DOI crossref	10.1021/acs.accounts.7b00444	10.1021/acs.accounts.7b00444
first author openalex	Piou	Piou

Citations

OpenAlex: 350
Scholar: none
DOI: 10.1021/acs.accounts.7b00444
OpenAlex: W2776710466

Match decisions

doi merged · 1.00 · Run 18

2018 External Regulation of Cobalt-Catalyzed Cycloaddition Polymerization with Visible Light. ACS Catalysis article journal CV OA GS

CV span

lines 632–633 · CV · published

632“External Regulation of Cobalt-Catalyzed Cycloaddition Polymerization with Visible Light.” B. D. Ravetz, K. E. Ruhl, T.633Rovis*. ACS Catal. 2018, 8, 5323-5327.

Institution fields

Peer reviewed: yes
First author: Ravetz
Co-authors: B. D. Ravetz; K. E. Ruhl; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	External Regulation of Cobalt-Catalyzed Cycloaddition Polymerization with Visible Light.	External Regulation of Cobalt-Catalyzed Cycloaddition Polymerization with Visible Light
year cv	2018	2018
venue crossref	ACS Catal.	ACS Catalysis	ACS Catalysis
kind cv	article	article
DOI crossref	10.1021/acscatal.8b01431	10.1021/acscatal.8b01431
first author openalex	Ravetz	Ravetz

Citations

OpenAlex: 37
Scholar: none
DOI: 10.1021/acscatal.8b01431
OpenAlex: W2799668337

Match decisions

doi merged · 1.00 · Run 18

2018 Ir(III)-Catalyzed Carbocarbation of Alkynes through Undirected Double C-H Bond Activation of Anisoles. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 629–630 · CV · published

629“Ir(III)-Catalyzed Carbocarbation of Alkynes through Undirected Double C-H Bond Activation of Anisoles.” F. Romanov-630Michailidis, B. D. Ravetz, D. W. Paley, T. Rovis*. J. Am. Chem. Soc. 2018, 140, 5370-5374.

Institution fields

Peer reviewed: yes
First author: Romanov-Michailidis
Co-authors: F. Romanov-Michailidis; B. D. Ravetz; D. W. Paley; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Ir(III)-Catalyzed Carbocarbation of Alkynes through Undirected Double C-H Bond Activation of Anisoles.	Ir(III)-Catalyzed Carbocarbation of Alkynes through Undirected Double C–H Bond Activation of Anisoles
year cv	2018	2018
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.8b02716	10.1021/jacs.8b02716
first author openalex	Romanov-Michailidis	Romanov‐Michailidis

Citations

OpenAlex: 114
Scholar: none
DOI: 10.1021/jacs.8b02716
OpenAlex: W2798036745

Match decisions

doi merged · 1.00 · Run 18

2018 Regiodivergent Iridium(III)-Catalyzed Diamination of Alkenyl Amides with Secondary Amines: Complementary Access to γ- or δ-Lactams Journal of the American Chemical Society article journal CV OA GS

CV span

lines 623–624 · CV · published

623"Regiodivergent Iridium(III)-Catalyzed Diamination of Alkenyl Amides with Secondary Amines: Complementary Access to γ-624or δ-Lactams”. J. H. Conway Jr. and T. Rovis*. J. Am. Chem. Soc. 2018, 140, 135-138.

Institution fields

Peer reviewed: yes
First author: Conway
Co-authors: J. H. Conway Jr.; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Regiodivergent Iridium(III)-Catalyzed Diamination of Alkenyl Amides with Secondary Amines: Complementary Access to γ- or δ-Lactams	Regiodivergent Iridium(III)-Catalyzed Diamination of Alkenyl Amides with Secondary Amines: Complementary Access to γ- or δ-Lactams
year cv	2018	2017
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.7b11455	10.1021/jacs.7b11455
first author openalex	Conway	Conway

Citations

OpenAlex: 101
Scholar: none
DOI: 10.1021/jacs.7b11455
OpenAlex: W2781036133

Match decisions

doi merged · 1.00 · Run 18

2018 Rhodium-Catalyzed Desymmetrization of meso-Glutaric Anhydrides to Access Enantioenriched anti,anti-Polypropionates. Synlett article journal CV OA GS

CV span

lines 626–627 · CV · published

626"Rhodium-Catalyzed Desymmetrization of meso-Glutaric Anhydrides to Access Enantioenriched anti,anti-Polypropionates." B.627M. Cochran, D. D. Henderson, S. M. Thullen and T. Rovis* Synlett 2018, 29, 306-309.

Institution fields

Peer reviewed: yes
First author: Cochran
Co-authors: B. M. Cochran; D. D. Henderson; S. M. Thullen; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Rhodium-Catalyzed Desymmetrization of meso-Glutaric Anhydrides to Access Enantioenriched anti,anti-Polypropionates.	Rhodium-Catalyzed Desymmetrization of meso-Glutaric Anhydrides to Access Enantioenriched anti,anti-Polypropionates
year cv	2018	2017
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0036-1591488	10.1055/s-0036-1591488
first author openalex	Cochran	Rovis

Citations

OpenAlex: 2
Scholar: none
DOI: 10.1055/s-0036-1591488
OpenAlex: W2765641181

Match decisions

doi merged · 1.00 · Run 18

2018 Stereodivergent Rhodium(III)-Catalyzed cis-Cyclopropanation Enabled by Multivariate Optimization. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 644–645 · CV · published

644“Stereodivergent Rhodium(III)-Catalyzed cis-Cyclopropanation Enabled by Multivariate Optimization.” T. Piou, F. Romanov-645Michailidis, M. A. Ashley, M. Romanova-Michailides, T. Rovis*. J. Am. Chem. Soc. 2018, 140, 9587-9593.

Institution fields

Peer reviewed: yes
First author: Piou
Co-authors: T. Piou; F. Romanov-Michailidis; M. A. Ashley; M. Romanova-Michailides; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Stereodivergent Rhodium(III)-Catalyzed cis-Cyclopropanation Enabled by Multivariate Optimization.	Stereodivergent Rhodium(III)-Catalyzed cis-Cyclopropanation Enabled by Multivariate Optimization
year cv	2018	2018
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.8b04243	10.1021/jacs.8b04243
first author openalex	Piou	Piou

Citations

OpenAlex: 66
Scholar: none
DOI: 10.1021/jacs.8b04243
OpenAlex: W2884934778

Match decisions

doi merged · 1.00 · Run 18

2018 The Catalytic Alkylative Desymmetrization of Anhydrides in a Formal Synthesis of Ionomycin. Synthesis article journal CV OA GS

CV span

lines 647–648 · CV · published

647“The Catalytic Alkylative Desymmetrization of Anhydrides in a Formal Synthesis of Ionomycin.” K. M. Oberg, B. M. Cochran,648M. J. Cook, T. Rovis*. Synthesis 2018, 4343-4350.

Institution fields

Peer reviewed: yes
First author: Oberg
Co-authors: K. M. Oberg; B. M. Cochran; M. J. Cook; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	The Catalytic Alkylative Desymmetrization of Anhydrides in a Formal Synthesis of Ionomycin.	The Catalytic Alkylative Desymmetrization of Anhydrides in a Formal Synthesis of Ionomycin
year cv	2018	2018
venue crossref	Synthesis	Synthesis
kind cv	article	article
DOI crossref	10.1055/s-0037-1610108	10.1055/s-0037-1610108
first author openalex	Oberg	Rovis

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1055/s-0037-1610108
OpenAlex: W2806383387

Match decisions

doi merged · 1.00 · Run 18

2017 A Mild Hydroaminoalkylation of Conjugated Dienes using a Unified Cobalt and Photoredox Catalytic System. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 604–605 · CV · published

604" A Mild Hydroaminoalkylation of Conjugated Dienes using a Unified Cobalt and Photoredox Catalytic System." S. M. Thullen605and T. Rovis*. J. Am. Chem. Soc. 2017, 139, 15504-15508.

Institution fields

Peer reviewed: yes
First author: Thullen
Co-authors: S. M. Thullen; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Mild Hydroaminoalkylation of Conjugated Dienes using a Unified Cobalt and Photoredox Catalytic System.	A Mild Hydroaminoalkylation of Conjugated Dienes Using a Unified Cobalt and Photoredox Catalytic System
year cv	2017	2017
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.7b09252	10.1021/jacs.7b09252
first author openalex	Thullen	Thullen

Citations

OpenAlex: 210
Scholar: none
DOI: 10.1021/jacs.7b09252
OpenAlex: W2765396001

Match decisions

doi merged · 1.00 · Run 18

2017 A Photochemical Two-Step Formal [5+2] Cycloaddition: A Condensation–Ring-Expansion Approach to Substituted Azepanes. Synlett article journal CV OA GS

CV span

lines 611–612 · CV · published

611" A Photochemical Two-Step Formal [5+2] Cycloaddition: A Condensation–Ring-Expansion Approach to Substituted612Azepanes." S. M. Thullen, D. M. Rubush, and T. Rovis*. Synlett 2017, 28, 2755-2758.

Institution fields

Peer reviewed: yes
First author: Thullen
Co-authors: S. M. Thullen; D. M. Rubush; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	A Photochemical Two-Step Formal [5+2] Cycloaddition: A Condensation–Ring-Expansion Approach to Substituted Azepanes.	A Photochemical Two-Step Formal [5+2] Cycloaddition: A Condensation–Ring-Expansion Approach to Substituted Azepanes
year cv	2017	2017
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0036-1589049	10.1055/s-0036-1589049
first author openalex	Thullen	Thullen

Citations

OpenAlex: 15
Scholar: none
DOI: 10.1055/s-0036-1589049
OpenAlex: W2729422992

Match decisions

doi merged · 1.00 · Run 18

2017 Correlating Reactivity and Selectivity to Cyclopentadienyl Ligand Properties in Rh(III)-Catalyzed C-H Activation Reactions: an Experimental and Computational Study. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 591–594 · CV · published

591"Correlating Reactivity and Selectivity to Cyclopentadienyl Ligand Properties in Rh(III)-Catalyzed C-H Activation Reactions:592an Experimental and Computational Study." T. Piou, F. Romanov-Michailidis, M. Romanova-Michailides, K. E. Jackson, N.593Semakul, T. D. Taggart, B. S. Newell, C. D. Rithner, R. S. Paton*, T. Rovis*. J. Am. Chem. Soc. 2017, 139, 1296-1310.594

Institution fields

Peer reviewed: yes
First author: Piou
Co-authors: T. Piou; F. Romanov-Michailidis; M. Romanova-Michailides; K. E. Jackson; N. Semakul; T. D. Taggart; B. S. Newell; C. D. Rithner; R. S. Paton*; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Correlating Reactivity and Selectivity to Cyclopentadienyl Ligand Properties in Rh(III)-Catalyzed C-H Activation Reactions: an Experimental and Computational Study.	Correlating Reactivity and Selectivity to Cyclopentadienyl Ligand Properties in Rh(III)-Catalyzed C–H Activation Reactions: An Experimental and Computational Study
year cv	2017	2017
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.6b11670	10.1021/jacs.6b11670
first author openalex	Piou	Piou

Citations

OpenAlex: 199
Scholar: none
DOI: 10.1021/jacs.6b11670
OpenAlex: W2569294683

Match decisions

doi merged · 1.00 · Run 18

2017 Directed γ-C(sp3)–H Alkylation of Carboxylic Acid Derivatives through Visible Light Photoredox Catalysis. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 601–602 · CV · published

601"Directed γ-C(sp3)–H Alkylation of Carboxylic Acid Derivatives through Visible Light Photoredox Catalysis." D.-F. Chen, J. C.602K. Chu, T. Rovis*. J. Am. Chem. Soc. 2017, 139, 14897-14900.

Institution fields

Peer reviewed: yes
First author: Chen
Co-authors: D.-F. Chen; J. C. K. Chu; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Directed γ-C(sp3)–H Alkylation of Carboxylic Acid Derivatives through Visible Light Photoredox Catalysis.	Directed γ-C(sp 3 )–H Alkylation of Carboxylic Acid Derivatives through Visible Light Photoredox Catalysis
year cv	2017	2017
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.7b09306	10.1021/jacs.7b09306
first author openalex	Chen	Chen

Citations

OpenAlex: 194
Scholar: none
DOI: 10.1021/jacs.7b09306
OpenAlex: W2763609595

Match decisions

doi merged · 1.00 · Run 18

2017 Dual Nickel- and Photoredox-Catalyzed Enantioselective Desymmetrization of Cyclic meso-Anhydrides. Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 595–596 · CV · published

595"Dual Nickel- and Photoredox-Catalyzed Enantioselective Desymmetrization of Cyclic meso-Anhydrides." E. E. Stache, T.596Rovis*, A. G. Doyle* Angew. Chem. Int. Ed. 2017, 56, 3679-3683.

Institution fields

Peer reviewed: yes
First author: Stache
Co-authors: E. E. Stache; T. Rovis*; A. G. Doyle*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Dual Nickel- and Photoredox-Catalyzed Enantioselective Desymmetrization of Cyclic meso-Anhydrides.	Dual Nickel‐ and Photoredox‐Catalyzed Enantioselective Desymmetrization of Cyclic meso‐AnhydridesDual Nickel‐ and Photoredox‐Catalyzed Enantioselective Desymmetrization of Cyclic meso‐Anhydrides
year cv	2017	20172017
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201700097	10.1002/anie.20170009710.1002/ange.201700097
first author openalex	Stache	StacheStache

Citations

OpenAlex: 120
Scholar: none
DOI: 10.1002/anie.201700097
OpenAlex: W2591403850

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2017 Enantioselective N-Heterocyclic Carbene-Catalyzed Nucleophilic Dearomatization of Alkyl Pyridiniums. Chemical Science article journal CV OA GS

CV span

lines 598–599 · CV · published

598"Enantioselective N-Heterocyclic Carbene-Catalyzed Nucleophilic Dearomatization of Alkyl Pyridiniums." D. M. Flanigan and599T. Rovis*. Chem. Sci. 2017, 8, 6566 – 6569.

Institution fields

Peer reviewed: yes
First author: Flanigan
Co-authors: D. M. Flanigan; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective N-Heterocyclic Carbene-Catalyzed Nucleophilic Dearomatization of Alkyl Pyridiniums.	Enantioselective N-heterocyclic carbene-catalyzed nucleophilic dearomatization of alkyl pyridiniums
year cv	2017	2017
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c7sc02648j	10.1039/c7sc02648j
first author openalex	Flanigan	Flanigan

Citations

OpenAlex: 81
Scholar: none
DOI: 10.1039/c7sc02648j
OpenAlex: W2743433926

Match decisions

doi merged · 1.00 · Run 18

2017 Experimental and Computational Gas Phase Acidities of Conjugate Acids of Triazolylidene Carbenes: Rationalizing Subtle Electronic Effects. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 607–609 · CV · published

607" Experimental and Computational Gas Phase Acidities of Conjugate Acids of Triazolylidene Carbenes: Rationalizing Subtle608Electronic Effects." Y. Niu, N. Wang, A. Muñoz, J. Xu, H. Zeng, T. Rovis*, J. K. Lee*. J. Am. Chem. Soc. 2017, 139,60914917-14930.

Institution fields

Peer reviewed: yes
First author: Niu
Co-authors: Y. Niu; N. Wang; A. Muñoz; J. Xu; H. Zeng; T. Rovis*; J. K. Lee*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Experimental and Computational Gas Phase Acidities of Conjugate Acids of Triazolylidene Carbenes: Rationalizing Subtle Electronic Effects.	Experimental and Computational Gas Phase Acidities of Conjugate Acids of Triazolylidene Carbenes: Rationalizing Subtle Electronic Effects
year cv	2017	2017
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.7b05229	10.1021/jacs.7b05229
first author openalex	Niu	Niu

Citations

OpenAlex: 38
Scholar: none
DOI: 10.1021/jacs.7b05229
OpenAlex: W2766519812

Match decisions

doi merged · 1.00 · Run 18

2017 Heptamethylindenyl (Ind*) enables diastereoselective benzamidation of cyclopropenes via Rh(III)-catalyzed C–H activation. Chemical Science article journal CV OA GS

CV span

lines 588–589 · CV · published

588"Heptamethylindenyl (Ind*) enables diastereoselective benzamidation of cyclopropenes via Rh(III)-catalyzed C–H activation."589N. Semakul, K. S. Jackson, R. S. Paton*, T. Rovis*. Chem. Sci. 2017, 8, 1015-1020.

Institution fields

Peer reviewed: yes
First author: Semakul
Co-authors: N. Semakul; K. S. Jackson; R. S. Paton*; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Heptamethylindenyl (Ind*) enables diastereoselective benzamidation of cyclopropenes via Rh(III)-catalyzed C–H activation.	Heptamethylindenyl (Ind*) enables diastereoselective benzamidation of cyclopropenes via Rh( iii )-catalyzed C–H activation
year cv	2017	2016
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c6sc02587k	10.1039/c6sc02587k
first author openalex	Semakul	Semakul

Citations

OpenAlex: 111
Scholar: none
DOI: 10.1039/c6sc02587k
OpenAlex: W2521144274

Match decisions

doi merged · 1.00 · Run 18

2017 N-Heterocyclic Carbene and Bronsted Acid Cooperative Catalysis for a Highly Enantioselective [4+2] Annulation. Synthesis article journal CV OA GS

CV span

lines 585–586 · CV · published

585"N-Heterocyclic Carbene and Bronsted Acid Cooperative Catalysis for a Highly Enantioselective [4+2] Annulation." D.-F. Chen586and T. Rovis*. Synthesis 2017, 49, 293-298.

Institution fields

Peer reviewed: yes
First author: Chen
Co-authors: D.-F. Chen; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	N-Heterocyclic Carbene and Bronsted Acid Cooperative Catalysis for a Highly Enantioselective [4+2] Annulation.	N-Heterocyclic Carbene and Chiral Brønsted Acid Cooperative Catalysis for a Highly Enantioselective [4+2] Annulation
year cv	2017	2016
venue crossref	Synthesis	Synthesis
kind cv	article	article
DOI crossref	10.1055/s-0036-1588349	10.1055/s-0036-1588349
first author openalex	Chen	Rovis

Citations

OpenAlex: 37
Scholar: none
DOI: 10.1055/s-0036-1588349
OpenAlex: W2549210927

Match decisions

doi merged · 1.00 · Run 18

2016 Amide-directed photoredox-catalysed C–C bond formation at unactivated sp3 C–H bonds. Nature article journal CV OA GS

CV span

lines 577–578 · CV · published

577" Amide-directed photoredox-catalysed C–C bond formation at unactivated sp3 C–H bonds." J. C. K. Chu and T. Rovis*. Nature5782016, 539, 272-275.

Institution fields

Peer reviewed: yes
First author: Chu
Co-authors: J. C. K. Chu; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Amide-directed photoredox-catalysed C–C bond formation at unactivated sp3 C–H bonds.	Amide-directed photoredox-catalysed C–C bond formation at unactivated sp3 C–H bonds
year cv	2016	2016
venue crossref	Nature	Nature
kind cv	article	article
DOI crossref	10.1038/nature19810	10.1038/nature19810
first author openalex	Chu	Chu

Citations

OpenAlex: 581
Scholar: none
DOI: 10.1038/nature19810
OpenAlex: W2531829504

Match decisions

doi merged · 1.00 · Run 18

2016 Catalysis with Stable Carbenes. Lewis Base Catalysis in Organic Synthesis chapter CV OA GS

CV span

lines 574–575 · CV · published

574"Catalysis with Stable Carbenes." D. M. Flanigan, N. A. White, K. M. Oberg, T. Rovis*.in Lewis Base Catalysis in Organic575Synthesis, E. Vedejs and S. E. Denmark, Editors. Wiley-VCH. 2016.

Institution fields

Peer reviewed: none
First author: Flanigan
Co-authors: D. M. Flanigan; N. A. White; K. M. Oberg; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: Wiley-VCH
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Catalysis with Stable Carbenes.	Catalysis with Stable Carbenes ( n ?→?π*)
year cv	2016	2016
venue cv	Lewis Base Catalysis in Organic Synthesis
kind cv	chapter	other
DOI openalex		10.1002/9783527675142.ch27
first author openalex	Flanigan	Flanigan

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1002/9783527675142.ch27
OpenAlex: W2511769262

Match decisions

fingerprint merged · 1.00 · Run 18

2016 Visible Light-Gated Cobalt Catalysis for a Spatially and Temporally Resolved [2+2+2] Cycloaddition. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 580–581 · CV · published

580"Visible Light-Gated Cobalt Catalysis for a Spatially and Temporally Resolved [2+2+2] Cycloaddition." K. E. Ruhl and T.581Rovis*. J. Am. Chem. Soc. 2016, 138, 15527-15530.

Institution fields

Peer reviewed: yes
First author: Ruhl
Co-authors: K. E. Ruhl; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Visible Light-Gated Cobalt Catalysis for a Spatially and Temporally Resolved [2+2+2] Cycloaddition.	Visible Light-Gated Cobalt Catalysis for a Spatially and Temporally Resolved [2+2+2] Cycloaddition
year cv	2016	2016
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.6b08792	10.1021/jacs.6b08792
first author openalex	Ruhl	Ruhl

Citations

OpenAlex: 92
Scholar: none
DOI: 10.1021/jacs.6b08792
OpenAlex: W2551079503

Match decisions

doi merged · 1.00 · Run 18

2015 Enantioselective Rhodium-Catalyzed Isomerization of 4-Iminocrotonates: Asymmetric Synthesis of a Unique Chiral Synthon. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 538–539 · CV · published

538"Enantioselective Rhodium-Catalyzed Isomerization of 4-Iminocrotonates: Asymmetric Synthesis of a Unique Chiral Synthon."539W.-Z. Zhang, J. C. K. Chu, K. M. Oberg, T. Rovis*. J. Am. Chem. Soc. 2015, 137, 553-555.

Institution fields

Peer reviewed: yes
First author: Zhang
Co-authors: W.-Z. Zhang; J. C. K. Chu; K. M. Oberg; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed Isomerization of 4-Iminocrotonates: Asymmetric Synthesis of a Unique Chiral Synthon.	Enantioselective Rhodium-Catalyzed Isomerization of 4-Iminocrotonates: Asymmetric Synthesis of a Unique Chiral Synthon
year cv	2015	2015
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja510348p	10.1021/ja510348p
first author openalex	Zhang	Zhang

Citations

OpenAlex: 24
Scholar: none
DOI: 10.1021/ja510348p
OpenAlex: W1518910744

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja510348p for the isomerization of 4-iminocrotonates.
doi merged · 1.00 · Run 18

2015 Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C-H Activation. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 554–555 · CV · published

554" Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C-H Activation." F. Romanov-555Michailidis, K. F. Sedillo, J. M. Neely, T. Rovis*. J. Am. Chem. Soc. 2015, 137, 8892-8895.

Institution fields

Peer reviewed: yes
First author: Romanov-Michailidis
Co-authors: F. Romanov-Michailidis; K. F. Sedillo; J. M. Neely; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C-H Activation.	Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C–H Activation
year cv	2015	2015
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.5b04946	10.1021/jacs.5b04946
first author openalex	Romanov-Michailidis	Romanov‐Michailidis

Citations

OpenAlex: 128
Scholar: none
DOI: 10.1021/jacs.5b04946
OpenAlex: W2257696768

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/jacs.5b04946 for the dihydropyridines synthesis paper.
doi merged · 1.00 · Run 18

2015 Influence of Electronic Effects on the Reactivity of Triazolylidene-Boryl Radicals: Consequences for the use of N-Heterocyclic Carbene Boranes in Organic and Polymer Synthesis. Chemistry – A European Journal article journal CV OA GS

CV span

lines 568–570 · CV · published

568"Influence of Electronic Effects on the Reactivity of Triazolylidene-Boryl Radicals: Consequences for the use of N-Heterocyclic569Carbene Boranes in Organic and Polymer Synthesis." S. Telitel, A.-L. Vallet, D. M. Flanigan, B. Graff, F. Morlet-Savary, T.570Rovis, J. Lalevée*, E. Lacote*. Chem. Eur. J. 2015, 21, 13772-13777.

Institution fields

Peer reviewed: yes
First author: Telitel
Co-authors: S. Telitel; A.-L. Vallet; D. M. Flanigan; B. Graff; F. Morlet-Savary; T. Rovis; J. Lalevée*; E. Lacote*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Influence of Electronic Effects on the Reactivity of Triazolylidene-Boryl Radicals: Consequences for the use of N-Heterocyclic Carbene Boranes in Organic and Polymer Synthesis.	Influence of Electronic Effects on the Reactivity of Triazolylidene‐Boryl Radicals: Consequences for the use of N‐Heterocyclic Carbene Boranes in Organic and Polymer Synthesis
year cv	2015	2015
venue crossref	Chem. Eur. J.	Chemistry - A European Journal	Chemistry – A European Journal
kind cv	article	article
DOI crossref	10.1002/chem.201500499	10.1002/chem.201500499
first author openalex	Telitel	Telitel

Citations

OpenAlex: 16
Scholar: none
DOI: 10.1002/chem.201500499
OpenAlex: W2113730857

Match decisions

doi merged · 1.00 · Run 18

2015 Ligand Design for Rh(III)-Catalyzed C–H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective Synthesis of Dihydroisoquinolones. Chemical Science article journal CV OA GS needs review

CV span

lines 534–536 · CV · published

534“Ligand Design for Rh(III)-Catalyzed C–H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective535Synthesis of Dihydroisoquinolones.” T. K. Hyster, D. M. Dalton, T. Rovis*. Chem. Sci. 2015, 6, 254-258. (PMCID:536PMC4256080)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; D. M. Dalton; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Ligand Design for Rh(III)-Catalyzed C–H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective Synthesis of Dihydroisoquinolones.	Ligand design for Rh( iii )-catalyzed C–H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones
year cv	2015	2014
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c4sc02590c	10.1039/c4sc02590c
first author openalex	Hyster	Hyster

Citations

OpenAlex: 140
Scholar: none
DOI: 10.1039/c4sc02590c
OpenAlex: W2124066328

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c4sc02590c for the ligand design for Rh(III)-catalyzed C-H activation.
doi merged · 1.00 · Run 18

2015 Natural Polarity Inverted. Nature article journal CV OA GS

CV span

lines 560–560 · CV · published

560"Natural Polarity Inverted." F. Romanov-Michailidis and T. Rovis*. Nature, 2015, 523, 417-418.

Institution fields

Peer reviewed: yes
First author: Romanov-Michailidis
Co-authors: F. Romanov-Michailidis; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Natural Polarity Inverted.	Natural polarity inverted
year cv	2015	2015
venue crossref	Nature	Nature
kind cv	article	article
DOI crossref	10.1038/523417a	10.1038/523417a
first author openalex	Romanov-Michailidis	Romanov‐Michailidis

Citations

OpenAlex: 15
Scholar: none
DOI: 10.1038/523417a
OpenAlex: W1014659247

Match decisions

doi merged · 1.00 · Run 18

2015 Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes. Chemical Reviews review journal CV OA GS needs review

CV span

lines 548–549 · CV · published

548"Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes." D. M. Flanigan, F. Romanov-Michailidis, N. A. White, T.549Rovis*. Chem. Rev. 2015, 115, 9307-9387.

Institution fields

Peer reviewed: yes
First author: Flanigan
Co-authors: D. M. Flanigan; F. Romanov-Michailidis; N. A. White; T. Rovis*
Subfield: other
Method: review
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes.	Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes
year cv	2015	2015
venue crossref	Chem. Rev.	Chemical Reviews	Chemical Reviews
kind cv	review	review
DOI crossref	10.1021/acs.chemrev.5b00060	10.1021/acs.chemrev.5b00060
first author openalex	Flanigan	Flanigan

Citations

OpenAlex: 2052
Scholar: none
DOI: 10.1021/acs.chemrev.5b00060
OpenAlex: W2299637886

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/acs.chemrev.5b00060 for the organocatalytic reactions review.
doi merged · 1.00 · Run 18

2015 Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 557–558 · CV · published

557" Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals." N. A.558White and T. Rovis*. J. Am. Chem. Soc. 2015, 137, 10112-10115.

Institution fields

Peer reviewed: yes
First author: White
Co-authors: N. A. White; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals.	Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals
year cv	2015	2015
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.5b06390	10.1021/jacs.5b06390
first author openalex	White	White

Citations

OpenAlex: 135
Scholar: none
DOI: 10.1021/jacs.5b06390
OpenAlex: W1163011906

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: excluded

2015 Rh-Catalyzed Intermolecular Syn-Carboamination of Alkenes via a Transient Directing Group. Nature article journal CV OA GS

CV span

lines 562–563 · CV · published

562" Rh-Catalyzed Intermolecular Syn-Carboamination of Alkenes via a Transient Directing Group." T. Piou and T. Rovis*. Nature5632015, 527, 86-90. (PMCID: PMC4636455).

Institution fields

Peer reviewed: yes
First author: Piou
Co-authors: T. Piou; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Rh-Catalyzed Intermolecular Syn-Carboamination of Alkenes via a Transient Directing Group.	Rhodium-catalysed syn-carboamination of alkenes via a transient directing group
year cv	2015	2015
venue openalex	Nature	Nature
kind cv	article	article
DOI openalex		10.1038/nature15691
first author openalex	Piou	Piou

Citations

OpenAlex: 248
Scholar: none
DOI: 10.1038/nature15691
OpenAlex: W2121041004

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1038/nature15691 for the rhodium-catalysed syn-carboamination.

2015 Rh(I)—Bisphosphine Catalyzed Asymmetric, Intermolecular Hydroheteroarylation of α-Substituted Acrylate Derivatives. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 541–542 · CV · published

541" Rh(I)—Bisphosphine Catalyzed Asymmetric, Intermolecular Hydroheteroarylation of α-Substituted Acrylate Derivatives." C.542M. Filloux and T. Rovis*. J. Am. Chem. Soc. 2015, 137, 508-517.

Institution fields

Peer reviewed: yes
First author: Filloux
Co-authors: C. M. Filloux; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(I)—Bisphosphine Catalyzed Asymmetric, Intermolecular Hydroheteroarylation of α-Substituted Acrylate Derivatives.	Rh(I)–Bisphosphine-Catalyzed Asymmetric, Intermolecular Hydroheteroarylation of α-Substituted Acrylate Derivatives
year cv	2015	2014
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja511445x	10.1021/ja511445x
first author openalex	Filloux	Filloux

Citations

OpenAlex: 110
Scholar: none
DOI: 10.1021/ja511445x
OpenAlex: W2286365455

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja511445x for the Rh(I)-bisphosphine catalyzed hydroheteroarylation.
doi merged · 1.00 · Run 18

2015 Rh(III)-Catalyzed Allylic C(sp3)−H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles. Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 565–566 · CV · published

565" Rh(III)-Catalyzed Allylic C(sp3)−H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles." A.566Archambeau and T. Rovis*. Angew. Chem. Int. Ed. 2015, 54, 13337-13340.

Institution fields

Peer reviewed: yes
First author: Archambeau
Co-authors: A. Archambeau; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(III)-Catalyzed Allylic C(sp3)−H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles.	Rhodium(III)‐Catalyzed Allylic C(sp3)–H Activation of Alkenyl Sulfonamides: Unexpected Formation of AzabicyclesRhodium(III)‐Catalyzed Allylic C(sp3)–H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles
year cv	2015	20152015
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201504150	10.1002/anie.20150415010.1002/ange.201504150
first author openalex	Archambeau	ArchambeauArchambeau

Also recorded as

W4232897708 (DOI 10.1002/ange.201504150) · platform twin · 2015 Rhodium(III)‐Catalyzed Allylic C(sp3)–H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles

Citations

OpenAlex: 81
Scholar: none
DOI: 10.1002/anie.201504150
OpenAlex: W2133971808

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2015 Rhodium(III)-Catalyzed C-H Activation: an Oxidative Heck-Type Reaction Directed by a Carboxylate Synlett article journal CV OA GS needs review

CV span

lines 551–552 · CV · published

551"Rhodium(III)-Catalyzed C-H Activation: an Oxidative Heck-Type Reaction Directed by a Carboxylate" T. A. Davis, C. Wang,552T. Rovis*. Synlett 2015, 1520-1524.

Institution fields

Peer reviewed: yes
First author: Davis
Co-authors: T. A. Davis; C. Wang; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Rhodium(III)-Catalyzed C-H Activation: an Oxidative Heck-Type Reaction Directed by a Carboxylate	Rhodium(III)-Catalyzed C–H Activation: An Oxidative Intramolecular Heck-Type Reaction Directed by a Carboxylate
year cv	2015	2015
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0034-1381006	10.1055/s-0034-1381006
first author openalex	Davis	Rovis

Citations

OpenAlex: 46
Scholar: none
DOI: 10.1055/s-0034-1381006
OpenAlex: W2344127674

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1055/s-0034-1381006 for the Rh(III)-catalyzed C-H activation.
doi merged · 1.00 · Run 18

2015 Zn-catalyzed Enantio- and Diastereoselective Formal [4+2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitroalkenes. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 544–546 · CV · published

544" Zn-catalyzed Enantio- and Diastereoselective Formal [4+2] Cycloaddition Involving Two Electron-Deficient Partners:545Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitroalkenes." J. C. K. Chu, D. M. Dalton, T. Rovis*. J. Am.546Chem. Soc. 2015, 137, 4445-4452.

Institution fields

Peer reviewed: yes
First author: Chu
Co-authors: J. C. K. Chu; D. M. Dalton; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Zn-catalyzed Enantio- and Diastereoselective Formal [4+2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitroalkenes.	Zn-Catalyzed Enantio- and Diastereoselective Formal [4 + 2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitro-Alkenes
year cv	2015	2015
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/jacs.5b00033	10.1021/jacs.5b00033
first author openalex	Chu	Chu

Citations

OpenAlex: 49
Scholar: none
DOI: 10.1021/jacs.5b00033
OpenAlex: W2019679586

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/jacs.5b00033 for the formal [4+2] cycloaddition paper.
doi merged · 1.00 · Run 18

2014 A Late Stage Strategy for the Functionalization of Triazolium-based NHC catalysts. Synlett article journal CV OA GS

CV span

lines 525–526 · CV · published

525"A Late Stage Strategy for the Functionalization of Triazolium-based NHC catalysts." K. E. Ozboya and T. Rovis*. Synlett 2014,5262665-2668. (PMCID: PMC4419734)

Institution fields

Peer reviewed: yes
First author: Ozboya
Co-authors: K. E. Ozboya; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	A Late Stage Strategy for the Functionalization of Triazolium-based NHC catalysts.	A Late-Stage Strategy for the Functionalization of Triazolium-Based NHC Catalysts
year cv	2014	2014
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0034-1379167	10.1055/s-0034-1379167
first author openalex	Ozboya	Rovis

Citations

OpenAlex: 21
Scholar: none
DOI: 10.1055/s-0034-1379167
OpenAlex: W1987579730

Match decisions

doi merged · 1.00 · Run 18

2014 A Stereoelectronic Basis for the Kinetic Resolution of N-Heterocycles with Chiral Acylating Reagents. Chemistry – A European Journal article journal CV OA GS needs review

CV span

lines 515–517 · CV · published

515“A Stereoelectronic Basis for the Kinetic Resolution of N-Heterocycles with Chiral Acylating Reagents.” S.-Y. Hsieh, B.516Wanner, P. Wheeler, A. M. Beauchemin, T. Rovis*, J. W. Bode*, Chem. Eur. J. 2014, 20, 7228-7231. (PMCID:517PMC4125202)

Institution fields

Peer reviewed: yes
First author: Hsieh
Co-authors: S.-Y. Hsieh; B. Wanner; P. Wheeler; A. M. Beauchemin; T. Rovis*; J. W. Bode*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Stereoelectronic Basis for the Kinetic Resolution of N-Heterocycles with Chiral Acylating Reagents.	Stereoelectronic Basis for the Kinetic Resolution of N‐Heterocycles with Chiral Acylating Reagents
year cv	2014	2014
venue crossref	Chem. Eur. J.	Chemistry - A European Journal	Chemistry – A European Journal
kind cv	article	article
DOI crossref	10.1002/chem.201402818	10.1002/chem.201402818
first author openalex	Hsieh	Hsieh

Citations

OpenAlex: 10
Scholar: none
DOI: 10.1002/chem.201402818
OpenAlex: W2089896698

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/chem.201402818 for the kinetic resolution of N-heterocycles.
doi merged · 1.00 · Run 18

2014 Cobaltate Anion Couples Terminal Dienes with Trifluoroacetic Anhydride: A Direct Fluoroacylation of 1,3-Dienes. Chem. Sci. article journal CV OA GS needs review

CV span

lines 512–513 · CV · published

512“Cobaltate Anion Couples Terminal Dienes with Trifluoroacetic Anhydride: A Direct Fluoroacylation of 1,3-Dienes.” B. L.513Kohn, T. Rovis*, Chem. Sci. 2014, 5, 2889 - 2892.

Institution fields

Peer reviewed: yes
First author: Kohn
Co-authors: B. L. Kohn; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Cobaltate Anion Couples Terminal Dienes with Trifluoroacetic Anhydride: A Direct Fluoroacylation of 1,3-Dienes.	Cobaltate anion couples terminal dienes with trifluoroacetic anhydride: a direct fluoroacylation of 1,3-dienes
year cv	2014	2014
venue crossref	Chem. Sci.	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c4sc00743c	10.1039/c4sc00743c
first author openalex	Kohn	Kohn

Citations

OpenAlex: 17
Scholar: none
DOI: 10.1039/c4sc00743c
OpenAlex: W2144840175

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c4sc00743c for the fluoroacylation of 1,3-dienes.
doi merged · 1.00 · Run 18

2014 Enantioselective N-Heterocyclic Carbene Catalyzed β-Hydroxylation of Enals Using Nitroarenes: An Atom Transfer Reaction that Proceeds via Single Electron Transfer. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 528–530 · CV · published

528"Enantioselective N-Heterocyclic Carbene Catalyzed β-Hydroxylation of Enals Using Nitroarenes: An Atom Transfer Reaction529that Proceeds via Single Electron Transfer." N. A. White and T. Rovis*. J. Am. Chem. Soc. 2014, 136, 14674-14677.530(PMCID: PMC4210054)

Institution fields

Peer reviewed: yes
First author: White
Co-authors: N. A. White; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective N-Heterocyclic Carbene Catalyzed β-Hydroxylation of Enals Using Nitroarenes: An Atom Transfer Reaction that Proceeds via Single Electron Transfer.	Enantioselective N-Heterocyclic Carbene-Catalyzed β-Hydroxylation of Enals Using Nitroarenes: An Atom Transfer Reaction That Proceeds via Single Electron Transfer
year cv	2014	2014
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja5080739	10.1021/ja5080739
first author openalex	White	White

Citations

OpenAlex: 216
Scholar: none
DOI: 10.1021/ja5080739
OpenAlex: W2043304555

Match decisions

doi merged · 1.00 · Run 18

2014 Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use of Taddol-pyrrolidine Phosphoramidite Organic Syntheses article journal CV OA GS

CV span

lines 508–510 · CV · published

508“Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use509of Taddol-pyrrolidine Phosphoramidite” K. M. Oberg, T. J. Martin, M. E. Oinen, D. M. Dalton, R. K. Friedman, J. M.510Neely, T. Rovis*, Org. Syn. 2014, 91, 150-161. (PMCID: PMC4205754)

Institution fields

Peer reviewed: yes
First author: Oberg
Co-authors: K. M. Oberg; T. J. Martin; M. E. Oinen; D. M. Dalton; R. K. Friedman; J. M. Neely; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use of Taddol-pyrrolidine Phosphoramidite	EnantioselectiveRhodium‐Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4‐Ethynylanisole: Preparation and Use of Taddol‐pyrrolidine Phosphoramidite
year cv	2014	2014
venue openalex	Org. Syn.	Organic Syntheses
kind cv	article	other
DOI openalex		10.1002/0471264229.os091.14
first author openalex	Oberg	Oberg

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/0471264229.os091.14
OpenAlex: W4256586385

Match decisions

fingerprint merged · 1.00 · Run 18

2014 Pyridine Synthesis by [4+2] Cycloadditions of 1-Azadienes: Hetero-Diels Alder and Transition Metal-Catalysed Approaches. Org. Chem. Front. article journal CV OA GS

CV span

lines 522–523 · CV · published

522“Pyridine Synthesis by [4+2] Cycloadditions of 1-Azadienes: Hetero-Diels Alder and Transition Metal-Catalysed Approaches.”523J. M. Neely and T. Rovis*. Org. Chem. Frontiers 2014, 1010-1015.

Institution fields

Peer reviewed: yes
First author: Neely
Co-authors: J. M. Neely; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Pyridine Synthesis by [4+2] Cycloadditions of 1-Azadienes: Hetero-Diels Alder and Transition Metal-Catalysed Approaches.	Pyridine synthesis by [4 + 2] cycloadditions of 1-azadienes: hetero-Diels Alder and transition metal-catalysed approaches
year cv	2014	2014
venue crossref	Org. Chem. Frontiers	Organic Chemistry Frontiers	Org. Chem. Front.
kind cv	article	article
DOI crossref	10.1039/c4qo00187g	10.1039/c4qo00187g
first author openalex	Neely	Neely

Citations

OpenAlex: 84
Scholar: none
DOI: 10.1039/c4qo00187g
OpenAlex: W2074022533

Match decisions

doi merged · 1.00 · Run 18

2014 Rapid Construction of (-)-Paroxetine and (-)-Femoxetine via N-Heterocyclic Carbene Catalyzed Homoenolate Addition to Nitroalkenes. Asian Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 504–506 · CV · published

504“Rapid Construction of (-)-Paroxetine and (-)-Femoxetine via N-Heterocyclic Carbene Catalyzed Homoenolate Addition to505Nitroalkenes.” N. A. White, K. E. Ozboya, D. M. Flanigan, T. Rovis*. Asian J. Org. Chem. 2014, 3, 442-444. (PMCID:506PMC4251551)

Institution fields

Peer reviewed: yes
First author: White
Co-authors: N. A. White; K. E. Ozboya; D. M. Flanigan; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rapid Construction of (-)-Paroxetine and (-)-Femoxetine via N-Heterocyclic Carbene Catalyzed Homoenolate Addition to Nitroalkenes.	Rapid Construction of (−)‐Paroxetine and (−)‐Femoxetine via an N‐Heterocyclic Carbene Catalyzed Homoenolate Addition to Nitroalkenes
year cv	2014	2014
venue crossref	Asian J. Org. Chem.	Asian Journal of Organic Chemistry	Asian Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1002/ajoc.201402031	10.1002/ajoc.201402031
first author openalex	White	White

Citations

OpenAlex: 22
Scholar: none
DOI: 10.1002/ajoc.201402031
OpenAlex: W2105469668

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/ajoc.201402031 for the rapid construction of paroxetine.
doi merged · 1.00 · Run 18

2014 Rh(III)-Catalyzed Cyclopropanation Initiated by C-H Activation: Ligand Development Enables a Diastereoselective [2+1] Annulation of N-Enoxyphthalimides and Alkenes. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 519–520 · CV · published

519“Rh(III)-Catalyzed Cyclopropanation Initiated by C-H Activation: Ligand Development Enables a Diastereoselective [2+1]520Annulation of N-Enoxyphthalimides and Alkenes.” T. Piou and T. Rovis*. J. Am. Chem. Soc. 2014, 136, 11292-11295.

Institution fields

Peer reviewed: yes
First author: Piou
Co-authors: T. Piou; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(III)-Catalyzed Cyclopropanation Initiated by C-H Activation: Ligand Development Enables a Diastereoselective [2+1] Annulation of N-Enoxyphthalimides and Alkenes.	Rh(III)-Catalyzed Cyclopropanation Initiated by C–H Activation: Ligand Development Enables a Diastereoselective [2 + 1] Annulation of N-Enoxyphthalimides and Alkenes
year cv	2014	2014
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja506579t	10.1021/ja506579t
first author openalex	Piou	Piou

Citations

OpenAlex: 163
Scholar: none
DOI: 10.1021/ja506579t
OpenAlex: W2318193487

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1021/ja506579t for the Rh(III)-catalyzed cyclopropanation article.

2014 Rh(III)-catalyzed Decarboxylative Coupling of Acrylic Acids with Unsaturated Oxime Esters: Carboxylic Acids Serve as Traceless Activators. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 501–502 · CV · published

501“Rh(III)-catalyzed Decarboxylative Coupling of Acrylic Acids with Unsaturated Oxime Esters: Carboxylic Acids Serve as502Traceless Activators.” J. M. Neely, T. Rovis*. J. Am. Chem. Soc. 2014, 136, 2735-2738.

Institution fields

Peer reviewed: yes
First author: Neely
Co-authors: J. M. Neely; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(III)-catalyzed Decarboxylative Coupling of Acrylic Acids with Unsaturated Oxime Esters: Carboxylic Acids Serve as Traceless Activators.	Rh(III)-Catalyzed Decarboxylative Coupling of Acrylic Acids with Unsaturated Oxime Esters: Carboxylic Acids Serve as Traceless Activators
year cv	2014	2014
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja412444d	10.1021/ja412444d
first author openalex	Neely	Neely

Citations

OpenAlex: 287
Scholar: none
DOI: 10.1021/ja412444d
OpenAlex: W2323495415

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja412444d for the decarboxylative coupling of acrylic acids.
doi merged · 1.00 · Run 18

2014 Stereoselective Synthesis of Dioxolanes and Oxazolidines via a Desymmetrization Acetalization/Michael Cascade. Synlett article journal CV OA GS needs review

CV span

lines 498–499 · CV · published

498“Stereoselective Synthesis of Dioxolanes and Oxazolidines via a Desymmetrization Acetalization/Michael Cascade.” D. M.499Rubush, T. Rovis*. Synlett, 2014, 713-717. (PMCID: PMC4422513)

Institution fields

Peer reviewed: yes
First author: Rubush
Co-authors: D. M. Rubush; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Stereoselective Synthesis of Dioxolanes and Oxazolidines via a Desymmetrization Acetalization/Michael Cascade.	Stereoselective Synthesis of Dioxolanes and Oxazolidines via a Desymmetrization Acetalization/Michael Cascade
year cv	2014	2014
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0033-1340669	10.1055/s-0033-1340669
first author openalex	Rubush	Rovis

Citations

OpenAlex: 17
Scholar: none
DOI: 10.1055/s-0033-1340669
OpenAlex: W2315142592

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1055/s-0033-1340669 for the synthesis of dioxolanes and oxazolidines.
doi merged · 1.00 · Run 18

2013 A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium (I) Catalyzed [2+2+2] Cycloaddition Employing a Cleavable Tether. Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 472–474 · CV · published

472“A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium (I) Catalyzed [2+2+2] Cycloaddition473Employing a Cleavable Tether.” T. J. Martin, T. Rovis*. Angew. Chem. Int. Ed. 2013, 52, 5368-5371. (PMCID:474PMC3820010)

Institution fields

Peer reviewed: yes
First author: Martin
Co-authors: T. J. Martin; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium (I) Catalyzed [2+2+2] Cycloaddition Employing a Cleavable Tether.	A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium(I)‐Catalyzed [2+2+2] Cycloaddition Employing a Cleavable TetherA Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium(I)‐Catalyzed [2+2+2] Cycloaddition Employing a Cleavable Tether
year cv	2013	20132013
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201301741	10.1002/anie.20130174110.1002/ange.201301741
first author openalex	Martin	MartinMartin

Also recorded as

W4251410434 (DOI 10.1002/ange.201301741) · same title · 2013 A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium(I)‐Catalyzed [2+2+2] Cycloaddition Employing a Cleavable Tether

Citations

OpenAlex: 33
Scholar: none
DOI: 10.1002/anie.201301741
OpenAlex: W2054791028

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.201301741 for the synthesis of polysubstituted piperidines.
doi merged · 1.00 · Run 18

2013 A Coupling of Benzamides and Donor/Acceptor Diazo-Compounds to form g-Lactams via Rh(III)-Catalyzed C-H Activation. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 476–477 · CV · published

476“A Coupling of Benzamides and Donor/Acceptor Diazo-Compounds to form g-Lactams via Rh(III)-Catalyzed C-H Activation.”477T. K. Hyster, K. E. Ruhl, T. Rovis*. J. Am. Chem. Soc. 2013, 135, 5364-5367. (PMCID: PMC3658175)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; K. E. Ruhl; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Coupling of Benzamides and Donor/Acceptor Diazo-Compounds to form g-Lactams via Rh(III)-Catalyzed C-H Activation.	A Coupling of Benzamides and Donor/Acceptor Diazo Compounds To Form γ-Lactams via Rh(III)-Catalyzed C–H Activation
year cv	2013	2013
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja402274g	10.1021/ja402274g
first author openalex	Hyster	Hyster

Citations

OpenAlex: 489
Scholar: none
DOI: 10.1021/ja402274g
OpenAlex: W2029708865

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja402274g for the coupling of benzamides to form gamma-lactams.
doi merged · 1.00 · Run 18

2013 A photoisomerization-coupled asymmetric Stetter reaction: application to the total synthesis of three diastereomers of (–)-cephalimysin A Chemical Science article journal CV OA GS

CV span

lines 466–467 · CV · published

466“A photoisomerization-coupled asymmetric Stetter reaction: application to the total synthesis of three diastereomers of (–)-467cephalimysin A.” S. P. Lathrop, T. Rovis*. Chem. Sci. 2013, 4, 1668-1673. (PMCID: PMC3820004)

Institution fields

Peer reviewed: yes
First author: Lathrop
Co-authors: S. P. Lathrop; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A photoisomerization-coupled asymmetric Stetter reaction: application to the total synthesis of three diastereomers of (–)-cephalimysin A	A photoisomerization-coupled asymmetric Stetter reaction: application to the total synthesis of three diastereomers of (−)-cephalimysin A
year cv	2013	2013
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c3sc22292f	10.1039/c3sc22292f
first author openalex	Lathrop	Lathrop

Citations

OpenAlex: 66
Scholar: none
DOI: 10.1039/c3sc22292f
OpenAlex: W1973889231

Match decisions

doi merged · 1.00 · Run 18

2013 Asymmetric NHC-Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry Via the Homoenolate Reactivity Pathway To Access d-Lactams. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 479–481 · CV · published

479“Asymmetric NHC-Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry Via the Homoenolate Reactivity480Pathway To Access d-Lactams.” N. A. White, D. A. DiRocco, T. Rovis*. J. Am. Chem. Soc. 2013, 135, 8504-8507.481(PMCID: PMC3723348)

Institution fields

Peer reviewed: yes
First author: White
Co-authors: N. A. White; D. A. DiRocco; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric NHC-Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry Via the Homoenolate Reactivity Pathway To Access d-Lactams.	Asymmetric N-Heterocyclic Carbene Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry via the Homoenolate Reactivity Pathway To Access δ-Lactams
year cv	2013	2013
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja403847e	10.1021/ja403847e
first author openalex	White	White

Citations

OpenAlex: 106
Scholar: none
DOI: 10.1021/ja403847e
OpenAlex: W2072202398

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/chin.201207236 for the Aldrichimica Acta article.

2013 Asymmetric NHC-catalyzed synthesis of a-fluoroamides from readily accessible a –fluoroenals Chemical Science article journal CV OA GS needs review

CV span

lines 463–464 · CV · published

463“Asymmetric NHC-catalyzed synthesis of a-fluoroamides from readily accessible a –fluoroenals.” P. Wheeler, H. Vora, T.464Rovis*. Chem. Sci. 2013, 4, 1674-1679. (PMCID: PMC4205762)

Institution fields

Peer reviewed: yes
First author: Wheeler
Co-authors: P. Wheeler; H. Vora; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric NHC-catalyzed synthesis of a-fluoroamides from readily accessible a –fluoroenals	Asymmetric NHC-catalyzed synthesis of α-fluoroamides from readily accessible α-fluoroenals
year cv	2013	2013
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c3sc00089c	10.1039/c3sc00089c
first author openalex	Wheeler	Wheeler

Citations

OpenAlex: 64
Scholar: none
DOI: 10.1039/c3sc00089c
OpenAlex: W2073325035

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c3sc00089c for the asymmetric NHC-catalyzed synthesis of alpha-fluoroamides.
doi merged · 1.00 · Run 18

2013 Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloids Core. Organic Letters article journal CV OA GS needs review

CV span

lines 486–487 · CV · published

486“Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine487Alkaloids Core.” D. M. Dalton, T. Rovis*. Org. Lett. 2013, 15, 2346-2349. (PMCID: PMC3809156)

Institution fields

Peer reviewed: yes
First author: Dalton
Co-authors: D. M. Dalton; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloids Core.	Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloid CoreCatalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloids Core
year cv	2013	20132013
venue crossref	Org. Lett.	Organic LettersOrganic Letters	Organic Letters
kind cv	article	articlearticle
DOI crossref	10.1021/ol400529k	10.1021/ol400529k10.1021/ol402427p
first author openalex	Dalton	DaltonDalton

Also recorded as

W4230792739 (DOI 10.1021/ol402427p) · same title · 2013 Catalytic, Asymmetric Indolizidinone Aza-Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloids Core

Citations

OpenAlex: 35
Scholar: none
DOI: 10.1021/ol400529k
OpenAlex: W2073770710

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ol400529k for the indolizidinone synthesis.
doi merged · 1.00 · Run 18

2013 Enantioselective Synthesis of the Tricyclic Core of FR901483 Featuring a Rh-Catalyzed [2+2+2] Cycloaddition Synthesis article journal CV OA GS

CV span

lines 457–458 · CV · published

457“Enantioselective Synthesis of the Tricyclic Core of FR901483 Featuring a Rh-Catalyzed [2+2+2] Cycloaddition.” S. Perreault458and T. Rovis*. Synthesis 2013, 45, 719-728. (PMCID: PMC4263289)

Institution fields

Peer reviewed: yes
First author: Perreault
Co-authors: S. Perreault; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Enantioselective Synthesis of the Tricyclic Core of FR901483 Featuring a Rh-Catalyzed [2+2+2] Cycloaddition	Enantioselective Synthesis of the Tricyclic Core of FR901483 Featuring a Rhodium-Catalyzed [2+2+2] Cycloaddition
year cv	2013	2013
venue crossref	Synthesis	Synthesis
kind cv	article	article
DOI crossref	10.1055/s-0032-1316786	10.1055/s-0032-1316786
first author openalex	Perreault	Rovis

Citations

OpenAlex: 18
Scholar: none
DOI: 10.1055/s-0032-1316786
OpenAlex: W2095468274

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1055/s-0032-1316786 for the synthesis of the tricyclic core of FR901483.

2013 Perfluorinated Taddol Phosphoramidite as an L,Z-Ligand on Rh(I) and Co(-I): Evidence for Bidentate Coordination via Metal-C6F5 Interaction Chemical Science article journal CV OA GS

CV span

lines 469–470 · CV · published

469“Perfluorinated Taddol Phosphoramidite as an L,Z-Ligand on Rh(I) and Co(-I): Evidence for Bidentate Coordination via Metal-470C6F5 Interaction.” D. M. Dalton, A. K. Rappé, T. Rovis*. Chem. Sci. 2013, 4, 2062-2070. (PMCID: PMC3650898)

Institution fields

Peer reviewed: yes
First author: Dalton
Co-authors: D. M. Dalton; A. K. Rappé; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Perfluorinated Taddol Phosphoramidite as an L,Z-Ligand on Rh(I) and Co(-I): Evidence for Bidentate Coordination via Metal-C6F5 Interaction	Perfluorinated Taddol phosphoramidite as an L,Z-ligand on Rh(i) and Co(−i): evidence for bidentate coordination via metal–C6F5 interaction
year cv	2013	2013
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c3sc50271f	10.1039/c3sc50271f
first author openalex	Dalton	Dalton

Citations

OpenAlex: 33
Scholar: none
DOI: 10.1039/c3sc50271f
OpenAlex: W2156372163

Match decisions

doi merged · 1.00 · Run 18

2013 Rh(III)-Catalyzed Regioselective Synthesis of Pyridines from Alkenes and a,b-Unsaturated Oxime Esters Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 460–461 · CV · published

460“Rh(III)-Catalyzed Regioselective Synthesis of Pyridines from Alkenes and a,b-Unsaturated Oxime Esters.” J. M. Neely, T.461Rovis*. J. Am. Chem. Soc. 2013, 135, 66-69. (PMCID: PMC3541442)

Institution fields

Peer reviewed: yes
First author: Neely
Co-authors: J. M. Neely; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rh(III)-Catalyzed Regioselective Synthesis of Pyridines from Alkenes and a,b-Unsaturated Oxime Esters	Rh(III)-Catalyzed Regioselective Synthesis of Pyridines from Alkenes and α,β-Unsaturated Oxime Esters
year cv	2013	2012
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja3104389	10.1021/ja3104389
first author openalex	Neely	Neely

Citations

OpenAlex: 338
Scholar: none
DOI: 10.1021/ja3104389
OpenAlex: W2020559236

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja3104389 for the synthesis of pyridines from alkenes.
doi merged · 1.00 · Run 18

2013 Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes. Synlett article journal CV OA GS

CV span

lines 489–490 · CV · published

489“Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes.” T. K. Hyster,490T. Rovis*. Synlett 2013, 1842-1844. (PMCID: PMC4206942)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes.	Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes
year cv	2013	2013
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0033-1339510	10.1055/s-0033-1339510
first author openalex	Hyster	Rovis

Citations

OpenAlex: 69
Scholar: none
DOI: 10.1055/s-0033-1339510
OpenAlex: W2950913482

Match decisions

doi merged · 1.00 · Run 18

2013 Rhodium(III)-Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck-type Reaction: Three Distinct Pathways Determined by an Amide Directing Group. Angewandte Chemie article journal CV OA GS

CV span

lines 492–494 · CV · published

492“Rhodium(III)-Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck-type Reaction: Three Distinct Pathways493Determined by an Amide Directing Group.” T. A. Davis, T. K. Hyster, T. Rovis*. Angew. Chem. Int. Ed. 2013, 52, 14431-49414435. (PMCID: PMC3896222)

Institution fields

Peer reviewed: yes
First author: Davis
Co-authors: T. A. Davis; T. K. Hyster; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium(III)-Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck-type Reaction: Three Distinct Pathways Determined by an Amide Directing Group.	Rhodium(III)‐Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck‐type Reaction: Three Distinct Pathways Determined by an Amide Directing GroupRhodium(III)‐Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck‐type Reaction: Three Distinct Pathways Determined by an Amide Directing Group
year cv	2013	20132013
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie
kind cv	article	articlearticle
DOI crossref	10.1002/ange.201307631	10.1002/anie.20130763110.1002/ange.201307631
first author openalex	Davis	DavisDavis

Citations

OpenAlex: 163
Scholar: none
DOI: 10.1002/ange.201307631
OpenAlex: W2098212677

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2013 SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes. Synlett article journal CV OA GS

CV span

lines 483–484 · CV · published

483“SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes.” X. Zhao, G. S. Glover, K. M.484Oberg, D. M. Dalton, T. Rovis*. Synlett 2013, 1229-1232. (PMCID: PMC3873771)

Institution fields

Peer reviewed: yes
First author: Zhao
Co-authors: X. Zhao; G. S. Glover; K. M. Oberg; D. M. Dalton; T. Rovis*
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes.	SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes
year cv	2013	2013
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0033-1338842	10.1055/s-0033-1338842
first author openalex	Zhao	Rovis

Citations

OpenAlex: 14
Scholar: none
DOI: 10.1055/s-0033-1338842
OpenAlex: W2059829500

Match decisions

doi merged · 1.00 · Run 18

2012 An Asymmetric Synthesis of 1,2,4-Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols through a Brønsted Acid Catalysis Cascade Journal of the American Chemical Society article journal CV OA GS

CV span

lines 445–447 · CV · published

445“An Asymmetric Synthesis of 1,2,4-Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols through a Brønsted446Acid Catalysis Cascade.” D. M. Rubush, M. A. Morges, B. J. Rose, D. H. Thamm, T. Rovis*. J. Am. Chem. Soc. 2012, 134,44713554-13557. (PMCID: PMC3433808)

Institution fields

Peer reviewed: yes
First author: Rubush
Co-authors: D. M. Rubush; M. A. Morges; B. J. Rose; D. H. Thamm; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	An Asymmetric Synthesis of 1,2,4-Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols through a Brønsted Acid Catalysis Cascade	An Asymmetric Synthesis of 1,2,4-Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols through a Brønsted Acid Catalysis Cascade
year cv	2012	2012
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja3052427	10.1021/ja3052427
first author openalex	Rubush	Rubush

Citations

OpenAlex: 212
Scholar: none
DOI: 10.1021/ja3052427
OpenAlex: W2093546262

Match decisions

doi merged · 1.00 · Run 18

2012 Biotinylated Rh(III) Complexes in Engineered Streptavidin for Accelerated Asymmetric C-H Activation Science article journal CV OA GS

CV span

lines 449–451 · CV · published

449“Biotinylated Rh(III) Complexes in Engineered Streptavidin for Accelerated Asymmetric C-H Activation.” T. K. Hyster, L.450Knörr, T. R. Ward*, T. Rovis*. Science, 2012, 338, 500-503. (PMCID: PMC3820005)451

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; L. Knörr; T. R. Ward; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Biotinylated Rh(III) Complexes in Engineered Streptavidin for Accelerated Asymmetric C-H Activation	Biotinylated Rh(III) Complexes in Engineered Streptavidin for Accelerated Asymmetric C–H Activation
year cv	2012	2012
venue crossref	Science	Science
kind cv	article	article
DOI crossref	10.1126/science.1226132	10.1126/science.1226132
first author openalex	Hyster	Hyster

Citations

OpenAlex: 814
Scholar: none
DOI: 10.1126/science.1226132
OpenAlex: W1987587964

Match decisions

doi merged · 1.00 · Run 18

2012 Catalytic Asymmetric Cross Aza-Benzoin Reactions of Aliphatic Aldehydes with N-Boc Imines Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 442–443 · CV · published

442“Catalytic Asymmetric Cross Aza-Benzoin Reactions of Aliphatic Aldehydes with N-Boc Imines.” D. A. DiRocco and T.443Rovis*. Angew. Chem. Int. Ed. 2012, 51, 5904-5906. (PMCID: PMC3423980)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Cross Aza-Benzoin Reactions of Aliphatic Aldehydes with N-Boc Imines	Catalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected IminesCatalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected Imines
year cv	2012	20122012
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201202442	10.1002/anie.20120244210.1002/ange.201202442
first author openalex	DiRocco	DiRoccoDiRocco

Also recorded as

W4233052779 (DOI 10.1002/ange.201202442) · platform twin · 2012 Catalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected Imines

Citations

OpenAlex: 135
Scholar: none
DOI: 10.1002/anie.201202442
OpenAlex: W2136349545

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.201206490 for the N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions.; The records share the same DOI 10.1002/chin.201239239 for the Exploiting Acyl and Enol Azoli…
doi merged · 1.00 · Run 18

2012 Catalytic Asymmetric Stetter Reaction of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 429–431 · CV · published

429“Catalytic Asymmetric Stetter Reaction of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into430the Success of the Catalyst.” D. A. DiRocco, E. L. Noey, K. N. Houk,* and T. Rovis*. Angew. Chem. Int. Ed. 2012, 51,4312391-2394. (PMCID: PMC3351195)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; E. L. Noey; K. N. Houk; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Stetter Reaction of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst	Catalytic Asymmetric Intermolecular Stetter Reactions of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the CatalystCatalytic Asymmetric Intermolecular Stetter Reactions of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst
year cv	2012	20122012
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201107597	10.1002/anie.20110759710.1002/ange.201107597
first author openalex	DiRocco	DiRoccoDiRocco

Also recorded as

W4248979581 (DOI 10.1002/ange.201107597) · platform twin · 2012 Catalytic Asymmetric Intermolecular Stetter Reactions of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst

Citations

OpenAlex: 131
Scholar: none
DOI: 10.1002/anie.201107597
OpenAlex: W2115262159

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2012 Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 439–441 · CV · published

439“Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and440Photoredox Catalysis.” D. A. DiRocco and T. Rovis*. J. Am. Chem. Soc. 2012, 134, 8094-8097. (PMCID: PMC3354013)441

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis	Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis
year cv	2012	2012
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja3030164	10.1021/ja3030164
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 571
Scholar: none
DOI: 10.1021/ja3030164
OpenAlex: W2334373491

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja3030164 for the alpha-acylation of tertiary amines.
doi merged · 1.00 · Run 18

2012 Exploiting Acyl and Enol Azolium Intermediates via N-Heterocyclic Carbene Catalyzed Reactions of Alpha-Reducible Aldehydes ChemInform article journal CV OA GS needs review

CV span

lines 433–435 · CV · published

433“Exploiting Acyl and Enol Azolium Intermediates via N-Heterocyclic Carbene Catalyzed Reactions of Alpha-Reducible434Aldehydes.” H. U. Vora, P. Wheeler, T. Rovis*. Adv. Synth. Catal. 2012, 354, 1617-1639. (PMCID: PMC3607462)435

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; P. Wheeler; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Exploiting Acyl and Enol Azolium Intermediates via N-Heterocyclic Carbene Catalyzed Reactions of Alpha-Reducible Aldehydes	ChemInform Abstract: Exploiting Acyl and Enol Azolium Intermediates via N‐Heterocyclic Carbene‐Catalyzed Reactions of α‐Reducible Aldehydes.
year cv	2012	2012
venue crossref	Adv. Synth. Catal.	ChemInform	ChemInform
kind cv	article	article
DOI crossref	10.1002/chin.201239239	10.1002/chin.201239239
first author openalex	Vora	Vora

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/chin.201239239
OpenAlex: W2951597644

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.201206490 for the N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions.; The records share the same DOI 10.1002/chin.201239239 for the Exploiting Acyl and Enol Azoli…
doi merged · 1.00 · Run 18

2012 Heterocycle Construction via Asymmetric Rhodium‐Catalyzed Cycloadditions Asymmetric Synthesis – The Essentials chapter CV OA GS needs review

CV span

lines 424–425 · CV · unverified · published

424“Heterocycle Construction via Asymmetric Rhodium Catalyzed Cycloadditions.” K. M. Oberg and T. Rovis*. In Asymmetric425Synthesis – The Essentials, M. Christmann, ed.

Institution fields

Peer reviewed: yes
First author: Oberg
Co-authors: K. M. Oberg; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title openalex	Heterocycle Construction via Asymmetric Rhodium Catalyzed Cycloadditions	Heterocycle Construction via Asymmetric Rhodium‐Catalyzed Cycloadditions
year openalex	2011	2012
venue cv	Asymmetric Synthesis – The Essentials
kind cv	chapter	other
DOI openalex		10.1002/9783527652235.ch38
first author openalex	Oberg	Oberg

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1002/9783527652235.ch38
OpenAlex: W1551791515

Match decisions

fingerprint merged · 1.00 · Run 18

2012 Isolable Analogues of the Breslow Intermediate Derived From Chiral Triazolylidene Carbenes Journal of the American Chemical Society article journal CV OA GS

CV span

lines 436–437 · CV · published

436“Isolable Analogues of the Breslow Intermediate Derived From Chiral Triazolylidene Carbenes.” D. A. DiRocco, K. M. Oberg,437T. Rovis*. J. Am. Chem. Soc. 2012, 134, 6143. (PMCID: PMC3336740)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; K. M. Oberg; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Isolable Analogues of the Breslow Intermediate Derived From Chiral Triazolylidene Carbenes	Isolable Analogues of the Breslow Intermediate Derived from Chiral Triazolylidene Carbenes
year cv	2012	2012
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja302031v	10.1021/ja302031v
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 168
Scholar: none
DOI: 10.1021/ja302031v
OpenAlex: W1968887784

Match decisions

doi merged · 1.00 · Run 18

2012 N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions with Simple Aliphatic Aldehydes Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 452–453 · CV · published

452“N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions with Simple Aliphatic Aldehydes.” X.453Zhao, K. E. Ruhl, T. Rovis*. Angew. Chem. Int. Ed. 2012, 51, 12330-12333. (PMCID: PMC3618466)

Institution fields

Peer reviewed: yes
First author: Zhao
Co-authors: X. Zhao; K. E. Ruhl; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions with Simple Aliphatic Aldehydes	N‐Heterocyclic‐Carbene‐Catalyzed Asymmetric Oxidative Hetero‐Diels–Alder Reactions with Simple Aliphatic AldehydesN‐Heterocyclic‐Carbene‐Catalyzed Asymmetric Oxidative Hetero‐Diels–Alder Reactions with Simple Aliphatic Aldehydes
year cv	2012	20122012
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.201206490	10.1002/anie.20120649010.1002/ange.201206490
first author openalex	Zhao	ZhaoZhao

Also recorded as

W4234566629 (DOI 10.1002/ange.201206490) · same title · 2012 N‐Heterocyclic‐Carbene‐Catalyzed Asymmetric Oxidative Hetero‐Diels–Alder Reactions with Simple Aliphatic Aldehydes

Citations

OpenAlex: 182
Scholar: none
DOI: 10.1002/anie.201206490
OpenAlex: W2168075041

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.201206490 for the N-Heterocyclic Carbene-Catalyzed Asymmetric Oxidative Hetero-Diels-Alder Reactions.; The records share the same DOI 10.1002/chin.201239239 for the Exploiting Acyl and Enol Azoli…
doi merged · 1.00 · Run 18

2011 An Improved Catalyst Architecture for Rhodium (III) Catalyzed C-H Activation and its Application to Pyridone Synthesis Chem. Sci. article journal CV OA GS needs review

CV span

lines 398–399 · CV · published

398“An Improved Catalyst Architecture for Rhodium (III) Catalyzed C-H Activation and its Application to Pyridone Synthesis.” T.399K. Hyster and T. Rovis*. Chem. Sci. 2011, 2, 1606-1610. (PMCID: PMC4286810)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	An Improved Catalyst Architecture for Rhodium (III) Catalyzed C-H Activation and its Application to Pyridone Synthesis	An improved catalyst architecture for rhodium(iii) catalyzed C–H activation and its application to pyridone synthesis
year cv	2011	2011
venue crossref	Chem. Sci.	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c1sc00235j	10.1039/c1sc00235j
first author openalex	Hyster	Hyster

Citations

OpenAlex: 238
Scholar: none
DOI: 10.1039/c1sc00235j
OpenAlex: W2044192713

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c1sc00235j for the improved catalyst architecture paper.
doi merged · 1.00 · Run 18

2011 Asymmetric Benzoin and Stetter Reactions ChemInform chapter journal CV OA GS needs review

CV span

lines 384–385 · CV · published

384“Asymmetric Benzoin and Stetter Reactions.” D. A. DiRocco and T. Rovis*. Stereoselective Synthesis 2, 2011, Thieme; p. 835-385862.

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: Thieme
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Asymmetric Benzoin and Stetter Reactions	ChemInform Abstract: Asymmetric Benzoin and Stetter Reactions
year cv	2011	2011
venue openalex	Stereoselective Synthesis 2	ChemInform
kind cv	chapter	article
DOI openalex		10.1002/chin.201140200
first author openalex	DiRocco	DiRocco

Also recorded as

W2047919783 (DOI 10.1002/chin.201031028) · platform twin · 2010 ChemInform Abstract: N‐Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of α‐Protio and α‐Deuterio α‐Chloro and α‐Fluoro Carboxylic Acids.
W2949077574 (DOI 10.1002/chin.201204089) · platform twin · 2011 ChemInform Abstract: N‐Heterocyclic Carbene and Broensted Acid Cooperative Catalysis: Asymmetric Synthesis of trans‐γ‐Lactams.
W2949139980 (DOI 10.1002/chin.201135163) · platform twin · 2011 ChemInform Abstract: Enantioselective Rhodium‐Catalyzed [4 + 2] Cycloaddition of α,β‐Unsaturated Imines and Isocyanates.
W2949520198 (DOI 10.1002/chin.201004051) · platform twin · 2010 ChemInform Abstract: Asymmetric Synthesis of Functionalized Cyclopentanones via a Multicatalytic Secondary Amine/N‐Heterocyclic Carbene Catalyzed Cascade Sequence.
W2949847368 (DOI 10.1002/chin.201102028) · platform twin · 2010 ChemInform Abstract: Rhodium‐Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C—H/N—H Activation.
W2950398379 (DOI 10.1002/chin.201151212) · platform twin · 2011 ChemInform Abstract: Organocatalytic Hydroacylation of Unactivated Alkenes
W2950683094 (DOI 10.1002/chin.201152050) · platform twin · 2011 ChemInform Abstract: Enamine/Carbene Cascade Catalysis in the Diastereo‐ and Enantioselective Synthesis of Functionalized Cyclopentanones.
W2950872597 (DOI 10.1002/chin.201149028) · platform twin · 2011 ChemInform Abstract: Catalytic Asymmetric Intermolecular Stetter Reaction of Enals with Nitroalkenes: Enhancement of Catalytic Efficiency Through Bifunctional Additives.
W2951247630 (DOI 10.1002/chin.201213139) · platform twin · 2012 ChemInform Abstract: Rhodium(III)‐Catalyzed Oxidative Carbonylation of Benzamides with Carbon Monoxide.
W2951336901 (DOI 10.1002/chin.201239166) · platform twin · 2012 ChemInform Abstract: Catalytic Asymmetric α‐Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N‐Heterocyclic Carbene and Photoredox Catalysis.
W2951528517 (DOI 10.1002/chin.201006177) · platform twin · 2010 ChemInform Abstract: Enantioselective Rhodium‐Catalyzed [4 + 2 + 2] Cycloaddition of Dienyl Isocyanates for the Synthesis of Bicyclic Azocine Rings.
W2951649109 (DOI 10.1002/chin.201148149) · platform twin · 2011 ChemInform Abstract: An Improved Catalyst Architecture for Rhodium(III)‐Catalyzed C—H Activation and Its Application to Pyridone Synthesis.
W2951666100 (DOI 10.1002/chin.201123226) · platform twin · 2011 ChemInform Abstract: Phosphoramidite—Rhodium Complexes as Catalysts for the Asymmetric [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Alkynes
W2952231134 (DOI 10.1002/chin.201243065) · platform twin · 2012 ChemInform Abstract: Catalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected Imines.
W2953270113 (DOI 10.1002/chin.201012138) · platform twin · 2010 ChemInform Abstract: Excess Substrate Is a Spectator Ligand in a Rhodium‐Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates with Tolanes.
W2953286037 (DOI 10.1002/chin.201007233) · platform twin · 2010 ChemInform Abstract: Multicomponent Cycloaddition Approaches in the Catalytic Asymmetric Synthesis of Alkaloid Targets
W4210384757 (DOI 10.1002/chin.201123231) · platform twin · 2011 ChemInform Abstract: Carbene Catalysts

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1002/chin.201140200
OpenAlex: W2054662438

Match decisions

gemini merged · 0.95 · Run 18 The records match on book chapter descriptions and authorship for asymmetric Stetter reactions.

2011 Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity ChemInform article journal CV OA GS

CV span

lines 421–422 · CV · published

421“Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity.” H. U. Vora and T. Rovis*. Aldrichimica Acta4222011, 44, 3-11. (PMCID: PMC4205590)

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity	ChemInform Abstract: Asymmetric N‐Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactions
year cv	2011	2012
venue crossref	Aldrichimica Acta	ChemInform	ChemInform
kind cv	article	article
DOI crossref	10.1002/chin.201207236	10.1002/chin.201207236
first author openalex	Vora	Vora

Also recorded as

W2951569270 · same title · 2011 Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity.

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1002/chin.201207236
OpenAlex: W1978289686

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/chin.201207236 for the Aldrichimica Acta article.

2011 Carbene Catalyzed Stetter Reactions Stereoselective Reactions of Carbonyl and Imino Groups chapter CV OA GS

CV span

lines 419–419 · CV · published

419“Carbene Catalyzed Stetter Reactions.” D. A. DiRocco and T. Rovis*. Asymmetric Organocatalysis 1, 2011, Thieme; p. 619-635.

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: Thieme
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Carbene Catalyzed Stetter Reactions	Asymmetric Intramolecular Stetter Reactions Catalyzed by N-Heterocyclic Carbenes
year cv	2011	2011
venue openalex	Asymmetric Organocatalysis 1	Stereoselective Reactions of Carbonyl and Imino Groups
kind cv	chapter	chapter
DOI openalex		10.1055/sos-sd-202-00465
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1055/sos-sd-202-00465
OpenAlex: W2502730102

Match decisions

gemini merged · 0.95 · Run 18 The records match on book chapter descriptions and authorship for asymmetric Stetter reactions.

2011 Catalytic Asymmetric Intermolecular Stetter Reaction of Enals with Nitroalkenes: Enhancement of Catalytic Efficiency Through Bifunctional Additives Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 394–396 · CV · published

394“Catalytic Asymmetric Intermolecular Stetter Reaction of Enals with Nitroalkenes: Enhancement of Catalytic Efficiency395Through Bifunctional Additives.” D. A. DiRocco and T. Rovis*. J. Am. Chem. Soc. 2011, 133, 10402-10405. (PMCID:396PMC3147302)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Intermolecular Stetter Reaction of Enals with Nitroalkenes: Enhancement of Catalytic Efficiency Through Bifunctional Additives	Catalytic Asymmetric Intermolecular Stetter Reaction of Enals with Nitroalkenes: Enhancement of Catalytic Efficiency through Bifunctional Additives
year cv	2011	2011
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja203810b	10.1021/ja203810b
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 225
Scholar: none
DOI: 10.1021/ja203810b
OpenAlex: W1982928176

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja203810b for the Stetter reaction of enals with nitroalkenes.
doi merged · 1.00 · Run 18

2011 Enamine/Carbene Cascade Catalysis in the Diastereo- and Enantioselective Synthesis of Functionalized Cyclopentanones Chemical Science article journal CV OA GS needs review

CV span

lines 404–405 · CV · published

404“Enamine/Carbene Cascade Catalysis in the Diastereo- and Enantioselective Synthesis of Functionalized Cyclopentanones.” K.405E. Ozboya and T. Rovis*. Chem. Sci. 2011, 2, 1835-1838. (PMCID: PMC3173771)

Institution fields

Peer reviewed: yes
First author: Ozboya
Co-authors: K. E. Ozboya; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enamine/Carbene Cascade Catalysis in the Diastereo- and Enantioselective Synthesis of Functionalized Cyclopentanones	Enamine/carbene cascade catalysis in the diastereo- and enantioselective synthesis of functionalized cyclopentanones
year cv	2011	2011
venue crossref	Chem. Sci.	Chemical Science	Chemical Science
kind cv	article	article
DOI crossref	10.1039/c1sc00175b	10.1039/c1sc00175b
first author openalex	Ozboya	Ozboya

Citations

OpenAlex: 107
Scholar: none
DOI: 10.1039/c1sc00175b
OpenAlex: W1974902037

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c1sc00175b for the enamine/carbene cascade catalysis.
doi merged · 1.00 · Run 18

2011 Enantioselective Rhodium-Catalyzed [4+2] Cycloaddition of Alpha, Beta-Unsaturated Imines and Isocyanates Journal of the American Chemical Society article journal CV OA GS

CV span

lines 391–392 · CV · published

391“Enantioselective Rhodium-Catalyzed [4+2] Cycloaddition of Alpha, Beta-Unsaturated Imines and Isocyanates.” K. M. Oberg,392T. Rovis*. J. Am. Chem. Soc. 2011, 133, 4785-4787. (PMCID: PMC3069138)

Institution fields

Peer reviewed: yes
First author: Oberg
Co-authors: K. M. Oberg; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed [4+2] Cycloaddition of Alpha, Beta-Unsaturated Imines and Isocyanates	Enantioselective Rhodium-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Isocyanates
year cv	2011	2011
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja200766k	10.1021/ja200766k
first author openalex	Oberg	Oberg

Citations

OpenAlex: 50
Scholar: none
DOI: 10.1021/ja200766k
OpenAlex: W2005972389

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja906641d for the [4+2+2] cycloaddition of dienyl isocyanates.

2011 Mechanistic Investigation of the Enantioselective Intramolecular Stetter Reaction: Proton Transfer is the First Irreversible Step Organic Letters article journal CV OA GS

CV span

lines 387–389 · CV · published

387“Mechanistic Investigation of the Enantioselective Intramolecular Stetter Reaction: Proton Transfer is the First Irreversible Step.”388J. L. Moore, A. P. Silvestri, J. Read de Alaniz, D. A. DiRocco, T. Rovis*. Org. Lett. 2011, 13, 1742-1745. (PMCID:389PMC3064720)

Institution fields

Peer reviewed: yes
First author: Moore
Co-authors: J. L. Moore; A. P. Silvestri; J. Read de Alaniz; D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Mechanistic Investigation of the Enantioselective Intramolecular Stetter Reaction: Proton Transfer is the First Irreversible Step	Mechanistic Investigation of the Enantioselective Intramolecular Stetter Reaction: Proton Transfer Is the First Irreversible Step
year cv	2011	2011
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol200256a	10.1021/ol200256a
first author openalex	Moore	Moore

Citations

OpenAlex: 99
Scholar: none
DOI: 10.1021/ol200256a
OpenAlex: W1968478013

Match decisions

doi merged · 1.00 · Run 18

2011 N-Heterocyclic Carbene and Brønsted Acid Cooperative Catalysis: Asymmetric Synthesis of trans-γ-Lactams Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 410–411 · CV · published

410“N-Heterocyclic Carbene and Brønsted Acid Cooperative Catalysis: Asymmetric Synthesis of trans-γ-Lactams.” X. Zhao, D. A.411DiRocco and T. Rovis*. J. Am. Chem. Soc. 2011, 133, 12466-12469. (PMCID: PMC3155423)

Institution fields

Peer reviewed: yes
First author: Zhao
Co-authors: X. Zhao; D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	N-Heterocyclic Carbene and Brønsted Acid Cooperative Catalysis: Asymmetric Synthesis of trans-γ-Lactams	N-Heterocyclic Carbene and Brønsted Acid Cooperative Catalysis: Asymmetric Synthesis of trans-γ-Lactams
year cv	2011	2011
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja205714g	10.1021/ja205714g
first author openalex	Zhao	Zhao

Citations

OpenAlex: 299
Scholar: none
DOI: 10.1021/ja205714g
OpenAlex: W1976545806

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja205714g for the NHC and Brønsted acid cooperative catalysis.
doi merged · 1.00 · Run 18

2011 Organocatalytic Hydroacylation of Unactivated Alkenes Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 407–408 · CV · published

407“Organocatalytic Hydroacylation of Unactivated Alkenes.” D. A. DiRocco and T. Rovis*. Angew. Chem. Int. Ed. 2011, 50, 7982.408(PMCID: PMC3427711)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Organocatalytic Hydroacylation of Unactivated Alkenes	Organocatalytic Hydroacylation of Unactivated Alkenes
year cv	2011	2011
venue crossref	Angew. Chem. Int. Ed.	Angewandte Chemie International Edition	Angewandte Chemie International Edition
kind cv	article	article
DOI crossref	10.1002/anie.201102920	10.1002/anie.201102920
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 48
Scholar: none
DOI: 10.1002/anie.201102920
OpenAlex: W2137160199

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.201102920 for the organocatalytic hydroacylation paper.
doi merged · 1.00 · Run 18

2011 Pyridine Synthesis from Oximes and Alkynes via Rhodium (III) Catalysis: Cp* and Cpt Provide Complementary Selectivity ChemInform article journal CV OA GS needs review

CV span

lines 413–414 · CV · published

413“Pyridine Synthesis from Oximes and Alkynes via Rhodium (III) Catalysis: Cp* and Cpt Provide Complementary Selectivity.” T.414K. Hyster and T. Rovis*. Chem. Commun. 2011, 47, 11846-11848. (PMCID: PMC3430144)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Pyridine Synthesis from Oximes and Alkynes via Rhodium (III) Catalysis: Cp* and Cpt Provide Complementary Selectivity	ChemInform Abstract: Pyridine Synthesis from Oximes and Alkynes via Rhodium(III) Catalysis: Cp* and Cpt Provide Complementary Selectivity.
year cv	2011	2012
venue crossref	Chem. Commun.	ChemInform	ChemInform
kind cv	article	article
DOI crossref	10.1002/chin.201211124	10.1002/chin.201211124
first author openalex	Hyster	Hyster

Also recorded as

W2156787066 (DOI 10.1002/chin.201307233) · platform twin · 2013 ChemInform Abstract: Carbene‐Catalyzed Stetter Reactions
W2949460445 (DOI 10.1002/chin.201334036) · platform twin · 2013 ChemInform Abstract: Asymmetric NHC‐Catalyzed Synthesis of α‐Fluoroamides from Readily Accessible α‐Fluoroenals.
W2951155336 (DOI 10.1002/chin.201342148) · platform twin · 2013 ChemInform Abstract: A Catalytic Asymmetric Synthesis of Polysubstituted Piperidines Using a Rhodium(I)‐Catalyzed [2 + 2 + 2] Cycloaddition Employing a Cleavable Tether.
W2951334054 (DOI 10.1002/chin.201346037) · platform twin · 2013 ChemInform Abstract: Asymmetric N‐Heterocyclic Carbene Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry via the Homoenolate Reactivity Pathway to Access δ‐Lactams.
W2951458289 (DOI 10.1002/chin.201337141) · platform twin · 2013 ChemInform Abstract: Catalytic, Asymmetric Indolizidinone Aza‐Quaternary Stereocenter Synthesis: Expedient Synthesis of the Cylindricine Alkaloid Core.
W2951847964 (DOI 10.1002/chin.201309165) · platform twin · 2013 ChemInform Abstract: An Asymmetric Synthesis of 1,2,4‐Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols Through a Broensted Acid Catalysis Cascade.
W2952465736 (DOI 10.1002/chin.201332248) · platform twin · 2013 ChemInform Abstract: Stable Carbenes: From “Laboratory Curiosities” to Catalysis Mainstays
W2952488980 (DOI 10.1002/chin.201324135) · platform twin · 2013 ChemInform Abstract: Rh(III)‐Catalyzed Regioselective Synthesis of Pyridines from Alkenes and α,β‐Unsaturated Oxime Esters.
W2952521645 (DOI 10.1002/chin.201322151) · platform twin · 2013 ChemInform Abstract: N‐Heterocyclic‐Carbene‐Catalyzed Asymmetric Oxidative Hetero‐Diels—Alder Reactions with Simple Aliphatic Aldehydes.

Citations

OpenAlex: 11
Scholar: none
DOI: 10.1002/chin.201211124
OpenAlex: W2953360017

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/c1cc15248c for the pyridine synthesis from oximes.

2011 Quantum Mechanical Investigation of the Effect of Catalyst Fluorination in the Intermolecular Asymmetric Stetter Reaction Journal of the American Chemical Society article journal CV OA GS

CV span

lines 401–402 · CV · published

401“Quantum Mechanical Investigation of the Effect of Catalyst Fluorination in the Intermolecular Asymmetric Stetter Reaction.” J.402M. Um, D. A. DiRocco, E. L. Noey, T. Rovis*, K. N. Houk*. J. Am. Chem. Soc. 2011, 133, 11249-11254.

Institution fields

Peer reviewed: yes
First author: Um
Co-authors: J. M. Um; D. A. DiRocco; E. L. Noey; T. Rovis; K. N. Houk
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Quantum Mechanical Investigation of the Effect of Catalyst Fluorination in the Intermolecular Asymmetric Stetter Reaction	Quantum Mechanical Investigation of the Effect of Catalyst Fluorination in the Intermolecular Asymmetric Stetter Reaction
year cv	2011	2011
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja202444g	10.1021/ja202444g
first author openalex	Um	Um

Citations

OpenAlex: 90
Scholar: none
DOI: 10.1021/ja202444g
OpenAlex: W1982429982

Match decisions

doi merged · 1.00 · Run 18

2011 Rhodium(III)-Catalyzed Oxidative Carbonylation of Benzamides with Carbon Monoxide Chemical Communications article journal CV OA GS

CV span

lines 416–417 · CV · published

416“Rhodium(III)-Catalyzed Oxidative Carbonylation of Benzamides with Carbon Monoxide.” Y. Du, T. K. Hyster, and T. Rovis*.417Chem. Commun. 2011, 47, 12074-12076. (PMCID: PMC3423973)

Institution fields

Peer reviewed: yes
First author: Du
Co-authors: Y. Du; T. K. Hyster; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium(III)-Catalyzed Oxidative Carbonylation of Benzamides with Carbon Monoxide	Rhodium(iii)-catalyzed oxidative carbonylation of benzamides with carbon monoxide
year cv	2011	2011
venue crossref	Chem. Commun.	Chemical Communications	Chemical Communications
kind cv	article	article
DOI crossref	10.1039/c1cc15843k	10.1039/c1cc15843k
first author openalex	Du	Du

Citations

OpenAlex: 167
Scholar: none
DOI: 10.1039/c1cc15843k
OpenAlex: W2051418642

Match decisions

doi merged · 1.00 · Run 18

2010 C-H Carboxylation takes Gold Nature Chemistry article journal CV OA GS

CV span

lines 380–380 · CV · published

380“C-H Carboxylation takes Gold.” D. M. Dalton, T. Rovis*. Nature Chem. 2010, 2, 710-711.

Institution fields

Peer reviewed: yes
First author: Dalton
Co-authors: D. M. Dalton; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	C-H Carboxylation takes Gold	C–H carboxylation takes gold
year cv	2010	2010
venue crossref	Nature Chem.	Nature Chemistry	Nature Chemistry
kind cv	article	article
DOI crossref	10.1038/nchem.815	10.1038/nchem.815
first author openalex	Dalton	Dalton

Citations

OpenAlex: 61
Scholar: none
DOI: 10.1038/nchem.815
OpenAlex: W2063752941

Match decisions

doi merged · 1.00 · Run 18

2010 Multicatalytic, Asymmetric Michael/Stetter Reaction of Salicylaldehydes and Activated Alkynes Proceedings of the National Academy of Sciences article journal CV OA GS

CV span

lines 371–372 · CV · published

371“Multicatalytic, Asymmetric Michael/Stetter Reaction of Salicylaldehydes and Activated Alkynes.” C. M. Filloux, S. P. Lathrop,372T. Rovis*. PNAS 2010, 107, 20666-20671. (PMCID: PMC2996425)

Institution fields

Peer reviewed: yes
First author: Filloux
Co-authors: C. M. Filloux; S. P. Lathrop; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Multicatalytic, Asymmetric Michael/Stetter Reaction of Salicylaldehydes and Activated Alkynes	Multicatalytic, asymmetric Michael/Stetter reaction of salicylaldehydes and activated alkynes
year cv	2010	2010
venue crossref	PNAS	Proceedings of the National Academy of Sciences	Proceedings of the National Academy of Sciences
kind cv	article	article
DOI crossref	10.1073/pnas.1002830107	10.1073/pnas.1002830107
first author openalex	Filloux	Filloux

Citations

OpenAlex: 130
Scholar: none
DOI: 10.1073/pnas.1002830107
OpenAlex: W2024954014

Match decisions

doi merged · 1.00 · Run 18

2010 N-Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of a-Protio and Deuterio a-Chloro and a-Fluoro Carboxylic Acids Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 361–362 · CV · published

361“N-Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of a-Protio and Deuterio a-Chloro and a-Fluoro362Carboxylic Acids.” H. U. Vora, T. Rovis*. J. Am. Chem. Soc. 2010, 132, 2860-2861. (PMCID: PMC2839412)

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	N-Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of a-Protio and Deuterio a-Chloro and a-Fluoro Carboxylic Acids	N-Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of α-Protio and α-Deuterio α-Chloro and α-Fluoro Carboxylic Acids
year cv	2010	2010
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja910281s	10.1021/ja910281s
first author openalex	Vora	Vora

Citations

OpenAlex: 164
Scholar: none
DOI: 10.1021/ja910281s
OpenAlex: W2953204233

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja910281s for the asymmetric hydration paper.
doi merged · 1.00 · Run 18

2010 Phosphoramidite-Rhodium Complexes as Catalysts for the Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes Pure and Applied Chemistry article journal CV OA GS

CV span

lines 364–366 · CV · published

364“Phosphoramidite-Rhodium Complexes as Catalysts for the Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates and365Alkynes.” R. K. Friedman, K. M. Oberg, D. M. Dalton, T. Rovis*. Pure Appl. Chem. 2010, 82, 1353-1364. (PMCID:366PMC2899493)

Institution fields

Peer reviewed: yes
First author: Friedman
Co-authors: R. K. Friedman; K. M. Oberg; D. M. Dalton; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Phosphoramidite-Rhodium Complexes as Catalysts for the Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes	Phosphoramidite-rhodium complexes as catalysts for the asymmetric [2 + 2 + 2] cycloaddition of alkenyl isocyanates and alkynes
year cv	2010	2010
venue crossref	Pure Appl. Chem.	Pure and Applied Chemistry	Pure and Applied Chemistry
kind cv	article	article
DOI crossref	10.1351/pac-con-09-12-09	10.1351/pac-con-09-12-09
first author openalex	Friedman	Friedman

Citations

OpenAlex: 36
Scholar: none
DOI: 10.1351/pac-con-09-12-09
OpenAlex: W2163300456

Match decisions

doi merged · 1.00 · Run 18

2010 Preparation Of Chiral And Achiral Triazolium Salts: Carbene Precursors With Demonstrated Synthetic Utility Organic Syntheses article journal CV OA GS

CV span

lines 368–369 · CV · published

368“Preparation Of Chiral And Achiral Triazolium Salts: Carbene Precursors With Demonstrated Synthetic Utility.” H. U. Vora, S.369P. Lathrop, N. T. Reynolds, M. S. Kerr, J. Read de Alaniz, T. Rovis*. Org. Syn. 2010, 87, 350.

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; S. P. Lathrop; N. T. Reynolds; M. S. Kerr; J. Read de Alaniz; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Preparation Of Chiral And Achiral Triazolium Salts: Carbene Precursors With Demonstrated Synthetic Utility	Preparation of Chiral and Achiral Triazolium Salts: Carbene Precursors with Demonstrated Synthetic Utility
year cv	2010	2010
venue crossref	Org. Syn.	Organic Syntheses	Organic Syntheses
kind cv	article	other
DOI crossref	10.1002/0471264229.os087.37	10.1002/0471264229.os087.37
first author openalex	Vora	Vora

Citations

OpenAlex: 10
Scholar: none
DOI: 10.1002/0471264229.os087.37
OpenAlex: W2141447524

Match decisions

doi merged · 1.00 · Run 18

2010 Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C-H/N-H Activation Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 374–375 · CV · published

374“Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C-H/N-H Activation.” T. K. Hyster, T. Rovis*.375J. Am. Chem. Soc. 2010, 132, 10565-10569. (PMCID: PMC2929375)

Institution fields

Peer reviewed: yes
First author: Hyster
Co-authors: T. K. Hyster; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C-H/N-H Activation	Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C−H/N−H Activation
year cv	2010	2010
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja103776u	10.1021/ja103776u
first author openalex	Hyster	Hyster

Citations

OpenAlex: 621
Scholar: none
DOI: 10.1021/ja103776u
OpenAlex: W1967897724

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja103776u for the rhodium-catalyzed oxidative cycloaddition.
doi merged · 1.00 · Run 18

2010 Stereospecific Polymerization of Chiral Oxazolidinone-Functionalized Alkenes Macromolecules article journal CV OA GS

CV span

lines 377–378 · CV · published

377“Stereospecific Polymerization of Chiral Oxazolidinone-Functionalized Alkenes.” G. M. Miyake, D. A. DiRocco, Q. Liu, K. M.378Oberg, E. Bayram, R. G. Finke, T. Rovis, E. Y.-X. Chen*. Macromolecules 2010, 43, 7504-7514.

Institution fields

Peer reviewed: yes
First author: Miyake
Co-authors: G. M. Miyake; D. A. DiRocco; Q. Liu; K. M. Oberg; E. Bayram; R. G. Finke; T. Rovis; E. Y.-X. Chen
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Stereospecific Polymerization of Chiral Oxazolidinone-Functionalized Alkenes	Stereospecific Polymerization of Chiral Oxazolidinone-Functionalized Alkenes
year cv	2010	2010
venue crossref	Macromolecules	Macromolecules
kind cv	article	article
DOI crossref	10.1021/ma101310n	10.1021/ma101310n
first author openalex	Miyake	Miyake

Citations

OpenAlex: 24
Scholar: none
DOI: 10.1021/ma101310n
OpenAlex: W2030073891

Match decisions

doi merged · 1.00 · Run 18

2009 Asymmetric Synthesis of Functionalized Cyclopentanones via a Multicatalytic Secondary Amine/N-Heterocyclic Carbene Catalyzed Cascade Sequence Journal of the American Chemical Society article journal CV OA GS

CV span

lines 344–346 · CV · published

344“Asymmetric Synthesis of Functionalized Cyclopentanones via a Multicatalytic Secondary Amine/N-Heterocyclic Carbene345Catalyzed Cascade Sequence.” S. P. Lathrop and T. Rovis*. J. Am. Chem. Soc. 2009, 131, 13628–13630. (PMCID:346PMC2785226)

Institution fields

Peer reviewed: yes
First author: Lathrop
Co-authors: S. P. Lathrop; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric Synthesis of Functionalized Cyclopentanones via a Multicatalytic Secondary Amine/N-Heterocyclic Carbene Catalyzed Cascade Sequence	Asymmetric Synthesis of Functionalized Cyclopentanones via a Multicatalytic Secondary Amine/N-Heterocyclic Carbene Catalyzed Cascade Sequence
year cv	2009	2009
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja905342e	10.1021/ja905342e
first author openalex	Lathrop	Lathrop

Citations

OpenAlex: 246
Scholar: none
DOI: 10.1021/ja905342e
OpenAlex: W2040170427

Match decisions

gemini merged · 0.99 · Run 18 The records share the same DOI 10.1021/ja905342e for the asymmetric synthesis of cyclopentanones.

2009 Beyond Reppe: Building Substituted Benzenes via [2+2+2] Cycloadditions of Alkynes Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 320–321 · CV · published

320“Beyond Reppe: Building Substituted Benzenes via [2+2+2] Cycloadditions of Alkynes.” B. R. Galan, T. Rovis*. Angew. Chem.321Int. Edit. 2009, 48, 2830-2834. (PMCID: PMC2898745)

Institution fields

Peer reviewed: yes
First author: Galan
Co-authors: B. R. Galan; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Beyond Reppe: Building Substituted Benzenes via [2+2+2] Cycloadditions of Alkynes	Beyond Reppe: Building Substituted Arenes by [2+2+2] Cycloadditions of Alkynes
year cv	2009	2009
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International Edition	Angewandte Chemie International Edition
kind cv	article	article
DOI crossref	10.1002/anie.200804651	10.1002/anie.200804651
first author openalex	Galan	Galan

Citations

OpenAlex: 284
Scholar: none
DOI: 10.1002/anie.200804651
OpenAlex: W2068927137

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.200804651 for the building of substituted benzenes.
doi merged · 1.00 · Run 18

2009 Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination Improves Selectivity Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 333–335 · CV · published

333“Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination334Improves Selectivity.” D. A. DiRocco, D. M. Dalton, K. M. Oberg, T. Rovis*. J. Am. Chem. Soc. 2009, 131, 10872-10874.335(PMCID: PMC2747345)

Institution fields

Peer reviewed: yes
First author: DiRocco
Co-authors: D. A. DiRocco; D. M. Dalton; K. M. Oberg; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination Improves Selectivity	Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination Improves Selectivity
year cv	2009	2009
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja904375q	10.1021/ja904375q
first author openalex	DiRocco	DiRocco

Citations

OpenAlex: 227
Scholar: none
DOI: 10.1021/ja904375q
OpenAlex: W2156702966

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1055/s-0029-1216654 for the intramolecular Stetter reaction article.; The records share the same DOI 10.1021/ja904375q for the intermolecular Stetter reaction of heterocyclic aldehydes.
doi merged · 1.00 · Run 18

2009 Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides Organic Letters article journal CV OA GS needs review

CV span

lines 330–331 · CV · published

330“Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides.” Q. Liu and T.331Rovis*. Org. Lett. 2009, 11, 2856-2859. (PMCID: PMC2782595)

Institution fields

Peer reviewed: yes
First author: Liu
Co-authors: Q. Liu; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides	Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides
year cv	2009	2009
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol901081a	10.1021/ol901081a
first author openalex	Liu	Liu

Citations

OpenAlex: 119
Scholar: none
DOI: 10.1021/ol901081a
OpenAlex: W1999718089

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ol901081a for the Stetter reaction of glyoxamide.
doi merged · 1.00 · Run 18

2009 Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity Journal of the American Chemical Society article journal CV OA GS

CV span

lines 348–351 · CV · published

348“Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic349Insights Lead to a Unified Model that Rationalizes Product Selectivity.” D. M. Dalton, K. M. Oberg, R. T. Yu, E. E. Lee, S.350Perreault, M. E. Oinen, M. L. Pease, G. Malik, and T. Rovis*. J. Am. Chem. Soc. 2009, 131, 15717-15728. (PMCID:351PMC2796191)

Institution fields

Peer reviewed: yes
First author: Dalton
Co-authors: D. M. Dalton; K. M. Oberg; R. T. Yu; E. E. Lee; S. Perreault; M. E. Oinen; M. L. Pease; G. Malik; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed [2+2+2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity	Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity
year cv	2009	2009
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja905065j	10.1021/ja905065j
first author openalex	Dalton	Dalton

Citations

OpenAlex: 76
Scholar: none
DOI: 10.1021/ja905065j
OpenAlex: W2036953607

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja905065j for the [2+2+2] cycloadditions paper.

2009 Enantioselective Rhodium-Catalyzed [4+2+2] Cycloaddition of Dienyl Isocyanates for the Synthesis of Bicyclic Azocine Rings Journal of the American Chemical Society article journal CV OA GS

CV span

lines 341–342 · CV · published

341“Enantioselective Rhodium-Catalyzed [4+2+2] Cycloaddition of Dienyl Isocyanates for the Synthesis of Bicyclic Azocine342Rings.” R. T. Yu, R. K. Friedman, T. Rovis*. J. Am. Chem. Soc. 2009, 131, 13250-13251. (PMCID: PMC2774260)

Institution fields

Peer reviewed: yes
First author: Yu
Co-authors: R. T. Yu; R. K. Friedman; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed [4+2+2] Cycloaddition of Dienyl Isocyanates for the Synthesis of Bicyclic Azocine Rings	Enantioselective Rhodium-Catalyzed [4+2+2] Cycloaddition of Dienyl Isocyanates for the Synthesis of Bicyclic Azocine Rings
year cv	2009	2009
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja906641d	10.1021/ja906641d
first author openalex	Yu	Yu

Citations

OpenAlex: 102
Scholar: none
DOI: 10.1021/ja906641d
OpenAlex: W2050771017

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja906641d for the [4+2+2] cycloaddition of dienyl isocyanates.

2009 Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-dimethylglutaric Anhydride Synthesis article journal CV OA GS

CV span

lines 314–315 · CV · published

314“Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-dimethylglutaric Anhydride.” M. J. Cook and T.315Rovis*. Synthesis: Practical Synthetic Procedure, 2009, 335.

Institution fields

Peer reviewed: yes
First author: Cook
Co-authors: M. J. Cook; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-dimethylglutaric Anhydride	Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-Dimethylglutaric Anhydride
year cv	2009	2008
venue crossref	Synthesis: Practical Synthetic Procedure	Synthesis	Synthesis
kind cv	article	article
DOI crossref	10.1055/s-0028-1083275	10.1055/s-0028-1083275
first author openalex	Cook	Rovis

Citations

OpenAlex: 4
Scholar: none
DOI: 10.1055/s-0028-1083275
OpenAlex: W2043238028

Match decisions

doi merged · 1.00 · Run 18

2009 Excess Substrate is a Spectator Ligand in a Rhodium-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates with Tolanes Organic Letters article journal CV OA GS

CV span

lines 353–354 · CV · published

353“Excess Substrate is a Spectator Ligand in a Rhodium-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates354with Tolanes.” M. E. Oinen, R. T. Yu, T. Rovis*. Org. Lett. 2009, 11, 4934-4937. (PMCID: PMC2777613)

Institution fields

Peer reviewed: yes
First author: Oinen
Co-authors: M. E. Oinen; R. T. Yu; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Excess Substrate is a Spectator Ligand in a Rhodium-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkenyl Isocyanates with Tolanes	Excess Substrate is a Spectator Ligand in a Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates with Tolanes
year cv	2009	2009
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol9020805	10.1021/ol9020805
first author openalex	Oinen	Oinen

Citations

OpenAlex: 37
Scholar: none
DOI: 10.1021/ol9020805
OpenAlex: W1970760473

Match decisions

doi merged · 1.00 · Run 18

2009 Lewis Base Catalysts 6: Carbene Catalysts Top. Curr. Chem. article CV OA GS needs review

CV span

lines 317–318 · CV · published

317“Lewis Base Catalysts 6: Carbene Catalysts.” J. L. Moore, T. Rovis*. Top. Curr. Chem. 2009, 290, 77-144. (PMCID:318PMC3820033)

Institution fields

Peer reviewed: yes
First author: Moore
Co-authors: J. L. Moore; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	Scholar
title cv	Lewis Base Catalysts 6: Carbene Catalysts
year cv	2009
venue cv	Top. Curr. Chem.
kind cv	article
first author cv	Moore

Citations

OpenAlex: none
Scholar: none

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1007/128_2008_18 for the carbene catalysts book chapter.

2009 Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides Tetrahedron article journal CV OA GS needs review

CV span

lines 311–312 · CV · published

311“Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic312anhydrides.” J. B. Johnson, M. J. Cook, T. Rovis*. Tetrahedron 2009, 65, 3202-3210.

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; M. J. Cook; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides	Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides
year cv	2009	2008
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/j.tet.2008.10.075	10.1016/j.tet.2008.10.075
first author openalex	Johnson	Johnson

Citations

OpenAlex: 19
Scholar: none
DOI: 10.1016/j.tet.2008.10.075
OpenAlex: W2950565267

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1016/j.tet.2008.10.075 for the ligand-differentiated Rh-catalyst systems.
doi merged · 1.00 · Run 18

2009 Multi-component Cycloaddition Approaches in the Catalytic Asymmetric Synthesis of Alkaloid Targets Chemical Society Reviews article journal CV OA GS

CV span

lines 356–357 · CV · published

356“Multi-component Cycloaddition Approaches in the Catalytic Asymmetric Synthesis of Alkaloid Targets.” S. Perreault and T.357Rovis*. Chem. Soc. Rev. 2009, 38, 3149-3159. (PMCID: PMC2893402)

Institution fields

Peer reviewed: yes
First author: Perreault
Co-authors: S. Perreault; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Multi-component Cycloaddition Approaches in the Catalytic Asymmetric Synthesis of Alkaloid Targets	Multi-component cycloaddition approaches in the catalytic asymmetric synthesis of alkaloid targets
year cv	2009	2009
venue crossref	Chem. Soc. Rev.	Chemical Society Reviews	Chemical Society Reviews
kind cv	article	review
DOI crossref	10.1039/b816702h	10.1039/b816702h
first author openalex	Perreault	Perreault

Citations

OpenAlex: 163
Scholar: none
DOI: 10.1039/b816702h
OpenAlex: W2002221932

Match decisions

doi merged · 1.00 · Run 18

2009 Predictable and Regioselective Insertion of Internal Unsymmetrical Alkynes in Rhodium-Catalyzed Cycloadditions with Alkenyl Isocyanates Journal of the American Chemical Society article journal CV OA GS

CV span

lines 337–339 · CV · published

337“Predictable and Regioselective Insertion of Internal Unsymmetrical Alkynes in Rhodium-Catalyzed Cycloadditions with338Alkenyl Isocyanates” R. Keller Friedman and T. Rovis*. J. Am. Chem. Soc. 2009, 131, 10775-10782. (PMCID:339PMC2737069)

Institution fields

Peer reviewed: yes
First author: Keller Friedman
Co-authors: R. Keller Friedman; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Predictable and Regioselective Insertion of Internal Unsymmetrical Alkynes in Rhodium-Catalyzed Cycloadditions with Alkenyl Isocyanates	Predictable and Regioselective Insertion of Internal Unsymmetrical Alkynes in Rhodium-Catalyzed Cycloadditions with Alkenyl Isocyanates
year cv	2009	2009
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja903899c	10.1021/ja903899c
first author openalex	Friedman	Friedman

Citations

OpenAlex: 71
Scholar: none
DOI: 10.1021/ja903899c
OpenAlex: W2056040117

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja905065j for the [2+2+2] cycloadditions paper.

2009 Regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of alkynes and isocyanates to form pyridones Tetrahedron article journal CV OA GS needs review

CV span

lines 327–328 · CV · published

327“Regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of alkynes and isocyanates to form pyridones.” K. M.328Oberg, E. E. Lee, T. Rovis*. Tetrahedron 2009, 65, 5056-5061. (PMCID: PMC3172821)

Institution fields

Peer reviewed: yes
First author: Oberg
Co-authors: K. M. Oberg; E. E. Lee; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of alkynes and isocyanates to form pyridones	Regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of alkynes and isocyanates to form pyridones
year cv	2009	2009
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/j.tet.2009.02.021	10.1016/j.tet.2009.02.021
first author openalex	Oberg	Oberg

Citations

OpenAlex: 44
Scholar: none
DOI: 10.1016/j.tet.2009.02.021
OpenAlex: W2071579212

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1016/j.tet.2009.02.021 for the regioselective [2+2+2] cycloaddition to form pyridones.
doi merged · 1.00 · Run 18

2009 The Catalytic Asymmetric Intramolecular Stetter Reaction Synlett article journal CV OA GS needs review

CV span

lines 308–309 · CV · published

308“The Catalytic Asymmetric Intramolecular Stetter Reaction.” J. Read de Alaniz, T. Rovis*. Synlett, 2009, 1189-1207. (PMCID:309PMC2888141)

Institution fields

Peer reviewed: yes
First author: Read de Alaniz
Co-authors: J. Read de Alaniz; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	The Catalytic Asymmetric Intramolecular Stetter Reaction	The Catalytic Asymmetric Intramolecular Stetter Reaction
year cv	2009	2009
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-0029-1216654	10.1055/s-0029-1216654
first author openalex	de Alaniz	Rovis

Citations

OpenAlex: 67
Scholar: none
DOI: 10.1055/s-0029-1216654
OpenAlex: W1974904191

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1055/s-0029-1216654 for the intramolecular Stetter reaction article.; The records share the same DOI 10.1021/ja904375q for the intermolecular Stetter reaction of heterocyclic aldehydes.
doi merged · 1.00 · Run 18

2009 Total Synthesis of Indolizidine Alkaloid (–)-209D: Overriding Substrate Bias in the Asymmetric Rhodium-Catalyzed [2+2+2] Cycloaddition Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 323–325 · CV · published

323“Total Synthesis of Indolizidine Alkaloid (–)-209D: Overriding Substrate Bias in the Asymmetric Rhodium-Catalyzed [2+2+2]324Cycloaddition.” R. T. Yu, E. E. Lee, G. Malik, T. Rovis*. Angew. Chem. Int. Edit. 2009, 48, 2379-2382. (PMCID:325PMC2747357)

Institution fields

Peer reviewed: yes
First author: Yu
Co-authors: R. T. Yu; E. E. Lee; G. Malik; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Total Synthesis of Indolizidine Alkaloid (–)-209D: Overriding Substrate Bias in the Asymmetric Rhodium-Catalyzed [2+2+2] Cycloaddition	Total Synthesis of Indolizidine Alkaloid (−)‐209D: Overriding Substrate Bias in the Asymmetric Rhodium‐Catalyzed [2+2+2] CycloadditionTotal Synthesis of Indolizidine Alkaloid (−)‐209D: Overriding Substrate Bias in the Asymmetric Rhodium‐Catalyzed [2+2+2] Cycloaddition
year cv	2009	20092009
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.200805455	10.1002/anie.20080545510.1002/ange.200805455
first author openalex	Yu	YuYu

Also recorded as

W4237917540 (DOI 10.1002/ange.200805455) · same title · 2009 Total Synthesis of Indolizidine Alkaloid (−)‐209D: Overriding Substrate Bias in the Asymmetric Rhodium‐Catalyzed [2+2+2] Cycloaddition

Citations

OpenAlex: 95
Scholar: none
DOI: 10.1002/anie.200805455
OpenAlex: W2135579479

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.200805455 for the total synthesis of indolizidine alkaloid.
doi merged · 1.00 · Run 18

2008 2-Phenyl-6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azonia-cyclopenta[c]fluorine tetrafluoroborate; 2-Pentafluorophenyl- 6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azoniacyclopenta[c]fluorene tetrafluoroborate; 6,7-Dihydro-2-phenyl-5- (phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride Encyclopedia of Reagents for Organic Synthesis chapter journal CV OA GS

CV span

lines 295–298 · CV · published

295“2-Phenyl-6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azonia-cyclopenta[c]fluorine tetrafluoroborate; 2-Pentafluorophenyl-2966,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azoniacyclopenta[c]fluorene tetrafluoroborate; 6,7-Dihydro-2-phenyl-5-297(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride.” S. P. Lathrop, H. U. Vora, T. Rovis*. Electronic Encyclopedia298of Reagents for Organic Synthesis, 2008.

Institution fields

Peer reviewed: yes
First author: Lathrop
Co-authors: S. P. Lathrop; H. U. Vora; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	2-Phenyl-6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azonia-cyclopenta[c]fluorine tetrafluoroborate; 2-Pentafluorophenyl- 6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azoniacyclopenta[c]fluorene tetrafluoroborate; 6,7-Dihydro-2-phenyl-5- (phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride	2-Phenyl-6,10b-dihydro-4H,5aH-5-oxa-3,10c-diaza-2-azonia-cyclopenta[c]fluorene tetrafluoroborate; 2-Pentafluorophenyl-6,10b-dihydro-4HM,5aH-5-oxa-3,10c-diaza-2-azoniacyclopenta[c]fluorene tetrafluoroborate; 6,7-Dihydro-2-phenyl-5-(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride
year cv	2008	2009
venue crossref	Electronic Encyclopedia of Reagents for Organic Synthesis	Encyclopedia of Reagents for Organic Synthesis	Encyclopedia of Reagents for Organic Synthesis
kind cv	chapter	chapter
DOI crossref	10.1002/047084289x.rn01060	10.1002/047084289x.rn01060
first author openalex	Lathrop	Rovis

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/047084289x.rn01060
OpenAlex: W2255979467

Match decisions

doi merged · 1.00 · Run 18

2008 A Diastereoselective Ring Contraction of 1,3-Dioxepins to 2,3,4-Trisubstituted and Tetrasubstituted Tetrahydrofurans. The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 267–268 · CV · published

267“A Diastereoselective Ring Contraction of 1,3-Dioxepins to 2,3,4-Trisubstituted and Tetrasubstituted Tetrahydrofurans.” C. G.268Nasveschuk and T. Rovis*. J. Org. Chem. 2008, 73, 612-617.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Diastereoselective Ring Contraction of 1,3-Dioxepins to 2,3,4-Trisubstituted and Tetrasubstituted Tetrahydrofurans.	A Diastereoselective Ring Contraction of 1,3-Dioxepins to 2,3,4-Trisubstituted and Tetrasubstituted Tetrahydrofurans
year cv	2008	2007
venue crossref	J. Org. Chem.	The Journal of Organic Chemistry	The Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1021/jo702071v	10.1021/jo702071v
first author openalex	Nasveschuk	Nasveschuk

Citations

OpenAlex: 20
Scholar: none
DOI: 10.1021/jo702071v
OpenAlex: W2952488761

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/jo702071v for the ring contraction of 1,3-dioxepins.
doi merged · 1.00 · Run 18

2008 A Rapid Total Synthesis of (+/-)-Sylvone. Synlett article journal CV OA GS needs review

CV span

lines 265–265 · CV · published

265“A Rapid Total Synthesis of (+/-)-Sylvone.” C. G. Nasveschuk and T. Rovis*. Synlett, 2008, 126-128.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	A Rapid Total Synthesis of (+/-)-Sylvone.	A Rapid Total Synthesis of (±)-Sylvone
year cv	2008	2007
venue crossref	Synlett	Synlett
kind cv	article	article
DOI crossref	10.1055/s-2007-990926	10.1055/s-2007-990926
first author openalex	Nasveschuk	Rovis

Citations

OpenAlex: 6
Scholar: none
DOI: 10.1055/s-2007-990926
OpenAlex: W2950227583

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1055/s-2007-990926 for the total synthesis of sylvone.
doi merged · 1.00 · Run 18

2008 Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Carbodiimides Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 283–284 · CV · published

283“Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Carbodiimides.” R. T. Yu and284T. Rovis*. J. Am. Chem. Soc. 2008, 130, 3262-3263. (PMCID: PMC2917183)

Institution fields

Peer reviewed: yes
First author: Yu
Co-authors: R. T. Yu; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Carbodiimides	Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2+2+2] Cycloaddition of Carbodiimides
year cv	2008	2008
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja710065h	10.1021/ja710065h
first author openalex	Yu	Yu

Citations

OpenAlex: 82
Scholar: none
DOI: 10.1021/ja710065h
OpenAlex: W2030027931

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja710065h for the synthesis of bicyclic amidines.
doi merged · 1.00 · Run 18

2008 Catalytic Asymmetric Intermolecular Stetter Reaction of Glyoxamides with Alkylidenemalonates Journal of the American Chemical Society article journal CV OA GS

CV span

lines 292–293 · CV · published

292“Catalytic Asymmetric Intermolecular Stetter Reaction of Glyoxamides with Alkylidenemalonates.” Q. Liu, S. Perreault, T.293Rovis*. J. Am. Chem. Soc. 2008, 130, 14066-14067. (PMCID: PMC2684863)

Institution fields

Peer reviewed: yes
First author: Liu
Co-authors: Q. Liu; S. Perreault; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Intermolecular Stetter Reaction of Glyoxamides with Alkylidenemalonates	Catalytic Asymmetric Intermolecular Stetter Reaction of Glyoxamides with Alkylidenemalonates
year cv	2008	2008
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja805680z	10.1021/ja805680z
first author openalex	Liu	Liu

Citations

OpenAlex: 266
Scholar: none
DOI: 10.1021/ja805680z
OpenAlex: W2012767952

Match decisions

doi merged · 1.00 · Run 18

2008 Catalytic Asymmetric Stetter Reaction Onto Vinylphosphine Oxides and Vinylphosphonates Organic Letters article journal CV OA GS needs review

CV span

lines 286–287 · CV · published

286“Catalytic Asymmetric Stetter Reaction Onto Vinylphosphine Oxides and Vinylphosphonates.” S. C. Cullen and T. Rovis*. Org.287Lett. 2008, 10, 3141-3144. (PMCID: PMC2746454)

Institution fields

Peer reviewed: yes
First author: Cullen
Co-authors: S. C. Cullen; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Catalytic Asymmetric Stetter Reaction Onto Vinylphosphine Oxides and Vinylphosphonates	Catalytic Asymmetric Stetter Reaction Onto Vinylphosphine Oxides and Vinylphosphonates
year cv	2008	2008
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol801047k	10.1021/ol801047k
first author openalex	Cullen	Cullen

Citations

OpenAlex: 126
Scholar: none
DOI: 10.1021/ol801047k
OpenAlex: W2015271873

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ol801047k for the catalytic asymmetric Stetter reaction paper.
doi merged · 1.00 · Run 18

2008 Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N-Aryl Substituent ChemInform review journal CV OA GS needs review

CV span

lines 273–274 · CV · published

273“Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N-Aryl Substituent.” T. Rovis. Chem.274Lett. 2008, 2-7. (Review)

Institution fields

Peer reviewed: yes
First author: Rovis
Co-authors: none
Subfield: other
Method: review
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N-Aryl Substituent	Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N-Aryl SubstituentChemInform Abstract: Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N‐Aryl Substituent
year cv	2008	20072008
venue crossref	Chem. Lett.	Chemistry LettersChemInform	ChemInform
kind cv	review	articlearticle
DOI crossref	10.1002/chin.200820249	10.1246/cl.2008.210.1002/chin.200820249
first author openalex	Rovis	RovisRovis

Also recorded as

W2066468340 (DOI 10.1002/chin.200817169) · platform twin · 2008 ChemInform Abstract: A Diastereoselective Intermolecular Heck Reaction of 1,3‐Dioxepins.
W2088735555 (DOI 10.1002/chin.200822206) · platform twin · 2008 ChemInform Abstract: A Rapid Total Synthesis of (.+‐.)‐Sylvone.
W2145491843 (DOI 10.1002/chin.200821105) · platform twin · 2008 ChemInform Abstract: A Diastereoselective Ring Contraction of 1,3‐Dioxepins to 2,3,4‐Trisubstituted and Tetrasubstituted Tetrahydrofurans.
W2149865684 (DOI 10.1002/chin.200933025) · platform twin · 2009 ChemInform Abstract: Ligand Differentiated Complementary Rh‐Catalyst Systems for the Enantioselective Desymmetrization of meso‐Cyclic Anhydrides.
W2153321707 (DOI 10.1246/cl.2008.2) · same title · 2007
W2949213325 (DOI 10.1002/chin.200944146) · platform twin · 2009 ChemInform Abstract: Regioselective Rhodium‐Catalyzed Intermolecular [2 + 2 + 2] Cycloaddition of Alkynes and Isocyanates to Form Pyridones.
W2949362134 (DOI 10.1002/chin.200814056) · platform twin · 2008 ChemInform Abstract: Nucleophilic Carbene and HOAt Relay Catalysis in an Amide Bond Coupling: An Orthogonal Peptide Bond Forming Reaction.
W2950016610 (DOI 10.1002/chin.200908072) · platform twin · 2009 ChemInform Abstract: Catalytic Asymmetric Intermolecular Stetter Reaction of Glyoxamides with Alkylidenemalonates.
W2950190209 (DOI 10.1002/chin.200915070) · platform twin · 2009 ChemInform Abstract: Nucleophilic Carbene Catalyzed Synthesis of 1,2 Amino Alcohols via Azidation of Epoxy Aldehydes.
W2950274056 (DOI 10.1002/chin.200848168) · platform twin · 2008 ChemInform Abstract: Catalytic Asymmetric Stetter Reaction onto Vinylphosphine Oxides and Vinylphosphonates.
W2950334862 (DOI 10.1002/chin.200831169) · platform twin · 2008 ChemInform Abstract: Asymmetric Synthesis of Bicyclic Amidines via Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Carbodiimides.
W2950424334 (DOI 10.1002/chin.200836151) · platform twin · 2008 ChemInform Abstract: Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes.
W2950650242 (DOI 10.1002/chin.200928139) · platform twin · 2009 ChemInform Abstract: Total Synthesis of Indolizidine Alkaloid (‐)‐209D: Overriding Substrate Bias in the Asymmetric Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition.
W2950991482 (DOI 10.1002/chin.200946076) · platform twin · 2009 ChemInform Abstract: Enantio‐ and Diastereoselective Intermolecular Stetter Reaction of Glycoxamide and Alkylidene Ketoamides.
W2951316441 (DOI 10.1002/chin.200830029) · platform twin · 2008 ChemInform Abstract: Scope of the Asymmetric Intramolecular Stetter Reaction Catalyzed by Chiral Nucleophilic Triazolinylidene Carbenes.
W2951545342 (DOI 10.1002/chin.200825207) · platform twin · 2008 ChemInform Abstract: Towards the Total Synthesis of FD‐838: Modular Enantioselective Assembly of the Core.
W2951550912 (DOI 10.1002/chin.200819240) · platform twin · 2008 ChemInform Abstract: The [1,3] O‐to‐C Rearrangement: Opportunities for Stereoselective Synthesis
W2951594418 (DOI 10.1002/chin.200911085) · platform twin · 2009 ChemInform Abstract: Nickel‐Catalyzed Reductive Carboxylation of Styrenes Using CO2.
W2951987120 (DOI 10.1002/chin.200820235) · platform twin · 2008 ChemInform Abstract: More than Bystanders: The Effect of Olefins on Transition‐Metal‐Catalyzed Cross‐Coupling Reactions.
W2952379141 (DOI 10.1002/chin.200927253) · platform twin · 2009 ChemInform Abstract: Beyond Reppe: Building Substituted Arenes by [2 + 2 + 2] Cycloadditions of Alkynes
W2952420778 (DOI 10.1002/chin.200934247) · platform twin · 2009 ChemInform Abstract: The Catalytic Asymmetric Intramolecular Stetter Reaction
W2952715385 (DOI 10.1002/chin.200815061) · platform twin · 2008 ChemInform Abstract: Alkene‐Directed Regioselective Nickel‐Catalyzed Cross‐Coupling of Cyclic Anhydrides with Diorganozinc Reagents.
W2952986173 (DOI 10.1002/chin.201002167) · platform twin · 2009 ChemInform Abstract: Predictable and Regioselective Insertion of Internal Unsymmetrical Alkynes in Rhodium‐Catalyzed Cycloadditions with Alkenyl Isocyanates.
W2953149033 (DOI 10.1002/chin.200823239) · platform twin · 2008 ChemInform Abstract: Enantioselective Cross‐Coupling of Anhydrides with Organozinc Reagents: The Controlled Formation of Carbon—Carbon Bonds Through the Nucleophilic Interception of Metalacycles
W2953149332 (DOI 10.1002/chin.201002027) · platform twin · 2009 ChemInform Abstract: Catalytic Asymmetric Intermolecular Stetter Reaction of Heterocyclic Aldehydes with Nitroalkenes: Backbone Fluorination Improves Selectivity.
W4251756271 (DOI 10.1002/chin.200933026) · platform twin · 2009 ChemInform Abstract: Ligand Differentiated Complementary Rh‐Catalyst Systems for the Enantioselective Desymmetrization of meso‐Cyclic Anhydrides.

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/chin.200820249
OpenAlex: W2952344726

Match decisions

gemini merged · 0.95 · Run 18 The records share identical title and ChemInform reference matching.

2008 Enantioselective Cross-Coupling of Anhydrides with Organozinc Reagents: The Controlled formation of Carbon-Carbon Bonds through the Nucleophilic Interception of Metalacycles Accounts of Chemical Research article journal CV OA GS needs review

CV span

lines 262–263 · CV · published

262“Enantioselective Cross-Coupling of Anhydrides with Organozinc Reagents: The Controlled formation of Carbon-Carbon Bonds263through the Nucleophilic Interception of Metalacycles”. J. B. Johnson, T. Rovis*. Acc. Chem. Res. 2008, 41, 327-338.

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Cross-Coupling of Anhydrides with Organozinc Reagents: The Controlled formation of Carbon-Carbon Bonds through the Nucleophilic Interception of Metalacycles	Enantioselective Cross-Coupling of Anhydrides with Organozinc Reagents: The Controlled Formation of Carbon−Carbon Bonds through the Nucleophilic Interception of Metalacycles
year cv	2008	2008
venue crossref	Acc. Chem. Res.	Accounts of Chemical Research	Accounts of Chemical Research
kind cv	article	article
DOI crossref	10.1021/ar700176t	10.1021/ar700176t
first author openalex	Johnson	Johnson

Citations

OpenAlex: 89
Scholar: none
DOI: 10.1021/ar700176t
OpenAlex: W2085225936

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ar700176t for the enantioselective cross-coupling of anhydrides review.
doi merged · 1.00 · Run 18

2008 Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes Organic Letters article journal CV OA GS needs review

CV span

lines 279–281 · CV · published

279“Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium-Catalyzed [2+2+2]280Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes.” E. E. Lee and T. Rovis*. Org. Lett. 2008, 10, 1231-1234.281(PMCID: PMC2747361)

Institution fields

Peer reviewed: yes
First author: Lee
Co-authors: E. E. Lee; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes	Enantioselective Synthesis of Indolizidines Bearing Quaternary Substituted Stereocenters via Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes
year cv	2008	2008
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol800086s	10.1021/ol800086s
first author openalex	Lee	Lee

Citations

OpenAlex: 80
Scholar: none
DOI: 10.1021/ol800086s
OpenAlex: W1966702581

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ol800086s for the synthesis of indolizidines.
doi merged · 1.00 · Run 18

2008 More than Bystanders: The Effect of Olefins on Transition Metal-Catalyzed Cross-Coupling Reactions. Angewandte Chemie International Edition review journal CV OA GS needs review

CV span

lines 259–260 · CV · published

259"More than Bystanders: The Effect of Olefins on Transition Metal-Catalyzed Cross-Coupling Reactions." J. B. Johnson, T.260Rovis*. Angew. Chem. Int. Edit. 2008, 47, 840-871. (Review)

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; T. Rovis
Subfield: other
Method: review
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	More than Bystanders: The Effect of Olefins on Transition Metal-Catalyzed Cross-Coupling Reactions.	More than Bystanders: The Effect of Olefins on Transition‐Metal‐Catalyzed Cross‐Coupling Reactions
year cv	2008	2007
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International Edition	Angewandte Chemie International Edition
kind cv	review	article
DOI crossref	10.1002/anie.200700278	10.1002/anie.200700278
first author openalex	Johnson	Johnson

Citations

OpenAlex: 372
Scholar: none
DOI: 10.1002/anie.200700278
OpenAlex: W2131086455

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.200700278 for the effect of olefins on cross-coupling.
doi merged · 1.00 · Run 18

2008 Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO2 Journal of the American Chemical Society article journal CV OA GS

CV span

lines 303–304 · CV · published

303“Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO2.” C. M. Williams, J. B. Johnson, T. Rovis*. J. Am. Chem.304Soc. 2008, 130, 14936-14937. (PMCID: PMC2928647)

Institution fields

Peer reviewed: yes
First author: Williams
Co-authors: C. M. Williams; J. B. Johnson; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO2	Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO 2
year cv	2008	2008
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja8062925	10.1021/ja8062925
first author openalex	Williams	Williams

Citations

OpenAlex: 413
Scholar: none
DOI: 10.1021/ja8062925
OpenAlex: W1985360331

Match decisions

doi merged · 1.00 · Run 18

2008 Nucleophilic Carbene Catalyzed Synthesis of 1,2 Amino Alcohols Via Azidation of Epoxy Aldehydes The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 300–301 · CV · published

300“Nucleophilic Carbene Catalyzed Synthesis of 1,2 Amino Alcohols Via Azidation of Epoxy Aldehydes.” H. U. Vora, J. R.301Moncecchi, O. Epstein, T. Rovis*. J. Org. Chem. 2008, 73, 9727-9731. (PMCID: PMC4222516)

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; J. R. Moncecchi; O. Epstein; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Nucleophilic Carbene Catalyzed Synthesis of 1,2 Amino Alcohols Via Azidation of Epoxy Aldehydes	Nucleophilic Carbene Catalyzed Synthesis of 1,2 Amino Alcohols Via Azidation of Epoxy Aldehydes
year cv	2008	2008
venue crossref	J. Org. Chem.	The Journal of Organic Chemistry	The Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1021/jo8020055	10.1021/jo8020055
first author openalex	Vora	Vora

Citations

OpenAlex: 41
Scholar: none
DOI: 10.1021/jo8020055
OpenAlex: W2089184527

Match decisions

doi merged · 1.00 · Run 18

2008 Scope of the Asymmetric Intramolecular Stetter Reaction Catalyzed by Chiral Nucleophilic Triazolinylidene Carbenes The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 289–290 · CV · published

289"Scope of the Asymmetric Intramolecular Stetter Reaction Catalyzed by Chiral Nucleophilic Triazolinylidene Carbenes." J. Read290de Alaniz, M. S. Kerr, J. L. Moore, T. Rovis*. J. Org. Chem. 2008, 73, 2033-2040. (PMCID: PMC4222522)

Institution fields

Peer reviewed: yes
First author: Read de Alaniz
Co-authors: J. Read de Alaniz; M. S. Kerr; J. L. Moore; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Scope of the Asymmetric Intramolecular Stetter Reaction Catalyzed by Chiral Nucleophilic Triazolinylidene Carbenes	Scope of the Asymmetric Intramolecular Stetter Reaction Catalyzed by Chiral Nucleophilic Triazolinylidene Carbenes
year cv	2008	2008
venue crossref	J. Org. Chem.	The Journal of Organic Chemistry	The Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1021/jo702313f	10.1021/jo702313f
first author openalex	de Alaniz	de Alaniz

Citations

OpenAlex: 155
Scholar: none
DOI: 10.1021/jo702313f
OpenAlex: W2082985076

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/jo702313f for the scope of asymmetric intramolecular Stetter reaction.
doi merged · 1.00 · Run 18

2008 The [1, 3] O to C Rearrangement: Opportunities for Stereoselective Synthesis. Org. Biomol. Chem. review journal CV OA GS needs review

CV span

lines 270–271 · CV · published

270“The [1, 3] O to C Rearrangement: Opportunities for Stereoselective Synthesis.” C. G. Nasveschuk and T. Rovis*. Org. Biomol.271Chem. 2008, 6, 240 - 254. (Review)

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; T. Rovis
Subfield: other
Method: review
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	The [1, 3] O to C Rearrangement: Opportunities for Stereoselective Synthesis.	The [1, 3] O-to-C rearrangement: opportunities for stereoselective synthesis
year cv	2008	2007
venue crossref	Org. Biomol. Chem.	Organic & Biomolecular Chemistry
kind cv	review	article
DOI crossref	10.1039/b714881j	10.1039/b714881j
first author openalex	Nasveschuk	Nasveschuk

Citations

OpenAlex: 87
Scholar: none
DOI: 10.1039/b714881j
OpenAlex: W2096936147

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/b714881j for the O-to-C rearrangement review.
doi merged · 1.00 · Run 18

2008 Towards the Total Synthesis of FD-838: Modular Enantioselective Assembly of the Core Chem. Commun. article journal CV OA GS needs review

CV span

lines 276–277 · CV · published

276“Towards the Total Synthesis of FD-838: Modular Enantioselective Assembly of the Core.” A. Orellana and T. Rovis*. Chem.277Commun. 2008, 730-732.

Institution fields

Peer reviewed: yes
First author: Orellana
Co-authors: A. Orellana; T. Rovis
Subfield: other
Method: other
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Towards the Total Synthesis of FD-838: Modular Enantioselective Assembly of the Core	Towards the total synthesis of FD-838: modular enantioselective assembly of the core
year cv	2008	2007
venue crossref	Chem. Commun.	Chemical Communications
kind cv	article	article
DOI crossref	10.1039/b716445a	10.1039/b716445a
first author openalex	Orellana	Orellana

Citations

OpenAlex: 57
Scholar: none
DOI: 10.1039/b716445a
OpenAlex: W2064803456

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1039/b716445a for the synthesis of FD-838.
doi merged · 1.00 · Run 18

2007 A Concise Synthesis of Eupomatilones 4, 6, and 7 via Rhodium-Catalyzed Enantioselective Desymmetrization of Cyclic meso- Anhydrides with in situ-Generated Organozinc Reagents. Angewandte Chemie International Edition article journal CV OA GS needs review

CV span

lines 241–243 · CV · published

241“A Concise Synthesis of Eupomatilones 4, 6, and 7 via Rhodium-Catalyzed Enantioselective Desymmetrization of Cyclic meso-242Anhydrides with in situ-Generated Organozinc Reagents.” J. B. Johnson, E. A. Bercot, C. M. Williams, T. Rovis*. Angew.243Chem. Int. Edit. 2007, 46, 4514.

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; E. A. Bercot; C. M. Williams; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Concise Synthesis of Eupomatilones 4, 6, and 7 via Rhodium-Catalyzed Enantioselective Desymmetrization of Cyclic meso- Anhydrides with in situ-Generated Organozinc Reagents.	A Concise Synthesis of Eupomatilones 4, 6, and 7 by Rhodium‐Catalyzed Enantioselective Desymmetrization of Cyclic meso Anhydrides with Organozinc Reagents Generated In SituA Concise Synthesis of Eupomatilones 4, 6, and 7 by Rhodium‐Catalyzed Enantioselective Desymmetrization of Cyclic meso Anhydrides with Organozinc Reagents Generated in situ.A Concise Synthesis of Eupomatilones 4, 6, and 7 by Rhodium‐Catalyzed Enantioselective Desymmetrization of Cyclic meso Anhydrides with Organozinc Reagents Generated In Situ
year cv	2007	200720072007
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International EditionChemInformAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticlearticle
DOI crossref	10.1002/anie.200700816	10.1002/anie.20070081610.1002/chin.20074003410.1002/ange.200700816
first author openalex	Johnson	JohnsonJohnsonJohnson

Also recorded as

W2952263598 (DOI 10.1002/chin.200740034) · platform twin · 2007 A Concise Synthesis of Eupomatilones 4, 6, and 7 by Rhodium‐Catalyzed Enantioselective Desymmetrization of Cyclic meso Anhydrides with Organozinc Reagents Generated in situ.
W4240957649 (DOI 10.1002/ange.200700816) · platform twin · 2007 A Concise Synthesis of Eupomatilones 4, 6, and 7 by Rhodium‐Catalyzed Enantioselective Desymmetrization of Cyclic meso Anhydrides with Organozinc Reagents Generated In Situ

Citations

OpenAlex: 52
Scholar: none
DOI: 10.1002/anie.200700816
OpenAlex: W2088967451

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.200700816 for the synthesis of eupomatilones via desymmetrization.; The records share the same DOI 10.1021/ja073269s for the desymmetrization of meso-3,5-dimethyl glutaric anhydride.
doi merged · 1.00 · Run 18

2007 A Diastereoselective Intermolecular Heck Reaction of 1,3-Dioxepins. Organic Letters article journal CV OA GS

CV span

lines 254–255 · CV · published

254“A Diastereoselective Intermolecular Heck Reaction of 1,3-Dioxepins.” C. G. Nasveschuk, J. D. Frein, N. T. Jui, T. Rovis*. Org.255Lett. 2007, 9, 5099-5102.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; J. D. Frein; N. T. Jui; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Diastereoselective Intermolecular Heck Reaction of 1,3-Dioxepins.	A Diastereoselective Intermolecular Heck Reaction of 1,3-Dioxepins
year cv	2007	2007
venue crossref	Org. Lett.	Organic Letters	Organic Letters
kind cv	article	article
DOI crossref	10.1021/ol702294u	10.1021/ol702294u
first author openalex	Nasveschuk	Nasveschuk

Citations

OpenAlex: 13
Scholar: none
DOI: 10.1021/ol702294u
OpenAlex: W2952829544

Match decisions

doi merged · 1.00 · Run 18

2007 Alkene-Directed Regioselective Nickel-Catalyzed Cross-Coupling of Cyclic Anhydrides with Diorganozinc Reagents. Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 251–252 · CV · published

251“Alkene-Directed Regioselective Nickel-Catalyzed Cross-Coupling of Cyclic Anhydrides with Diorganozinc Reagents.” R. L.252Rogers, J. L. Moore, T. Rovis*. Angew. Chem. Int. Edit. 2007, 47, 9301-9304.

Institution fields

Peer reviewed: yes
First author: Rogers
Co-authors: R. L. Rogers; J. L. Moore; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Alkene-Directed Regioselective Nickel-Catalyzed Cross-Coupling of Cyclic Anhydrides with Diorganozinc Reagents.	Alkene‐Directed Regioselective Nickel‐Catalyzed Cross‐Coupling of Cyclic Anhydrides with Diorganozinc ReagentsAlkene‐Directed Regioselective Nickel‐Catalyzed Cross‐Coupling of Cyclic Anhydrides with Diorganozinc Reagents
year cv	2007	20072007
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International EditionAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticle
DOI crossref	10.1002/anie.200703124	10.1002/anie.20070312410.1002/ange.200703124
first author openalex	Rogers	RogersRogers

Also recorded as

W4254558599 (DOI 10.1002/ange.200703124) · same title · 2007 Alkene‐Directed Regioselective Nickel‐Catalyzed Cross‐Coupling of Cyclic Anhydrides with Diorganozinc Reagents

Citations

OpenAlex: 34
Scholar: none
DOI: 10.1002/anie.200703124
OpenAlex: W2169246275

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2007 Enantioselective Synthesis of Hydrobenzofuranones Using an Asymmetric Desymmetrizing Intramolecular Stetter Reaction of Cyclohexadienones. Organic Process Research & Development article journal CV OA GS needs review

CV span

lines 238–239 · CV · published

238“Enantioselective Synthesis of Hydrobenzofuranones Using an Asymmetric Desymmetrizing Intramolecular Stetter Reaction of239Cyclohexadienones.” Q. Liu and T. Rovis*. Org. Proc. Res. Dev. 2007, 11, 598-604. (PMCID: PMC2709411)

Institution fields

Peer reviewed: yes
First author: Liu
Co-authors: Q. Liu; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Synthesis of Hydrobenzofuranones Using an Asymmetric Desymmetrizing Intramolecular Stetter Reaction of Cyclohexadienones.	Enantioselective Synthesis of Hydrobenzofuranones Using an Asymmetric Desymmetrizing Intramolecular Stetter Reaction of Cyclohexadienones
year cv	2007	2007
venue crossref	Org. Proc. Res. Dev.	Organic Process Research & Development	Organic Process Research & Development
kind cv	article	article
DOI crossref	10.1021/op600278f	10.1021/op600278f
first author openalex	Liu	Liu

Citations

OpenAlex: 71
Scholar: none
DOI: 10.1021/op600278f
OpenAlex: W2033101321

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/op600278f for the enantioselective synthesis of hydrobenzofuranones.
doi merged · 1.00 · Run 18

2007 Ligand Dependent Catalytic Cycle and Role of Styrene in Nickel-Catalyzed Anhydride Cross-Coupling: Evidence for Turnover Limiting Reductive Elimination. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 234–236 · CV · published

234“Ligand Dependent Catalytic Cycle and Role of Styrene in Nickel-Catalyzed Anhydride Cross-Coupling: Evidence for Turnover235Limiting Reductive Elimination.” J. B. Johnson, E. A. Bercot, J. M. Rowley, G. W. Coates and T. Rovis*. J. Am. Chem.236Soc. 2007, 129, 2718-2725.

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; E. A. Bercot; J. M. Rowley; G. W. Coates; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Ligand Dependent Catalytic Cycle and Role of Styrene in Nickel-Catalyzed Anhydride Cross-Coupling: Evidence for Turnover Limiting Reductive Elimination.	Ligand-Dependent Catalytic Cycle and Role of Styrene in Nickel-Catalyzed Anhydride Cross-Coupling: Evidence for Turnover-Limiting Reductive Elimination
year cv	2007	2007
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja067845g	10.1021/ja067845g
first author openalex	Johnson	Johnson

Citations

OpenAlex: 86
Scholar: none
DOI: 10.1021/ja067845g
OpenAlex: W2086514207

Match decisions

doi merged · 1.00 · Run 18

2007 Nucleophilic Carbene and HOAt Relay Catalysis in a Waste Free Amide Bond Coupling: An Orthogonal Peptide Bond Forming Reaction. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 248–249 · CV · published

248“Nucleophilic Carbene and HOAt Relay Catalysis in a Waste Free Amide Bond Coupling: An Orthogonal Peptide Bond Forming249Reaction.” H. U. Vora and T. Rovis*. J. Am. Chem. Soc. 2007, 129, 13796-13797. (PMCID: PMC2727858)

Institution fields

Peer reviewed: yes
First author: Vora
Co-authors: H. U. Vora; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Nucleophilic Carbene and HOAt Relay Catalysis in a Waste Free Amide Bond Coupling: An Orthogonal Peptide Bond Forming Reaction.	Nucleophilic Carbene and HOAt Relay Catalysis in an Amide Bond Coupling: An Orthogonal Peptide Bond Forming Reaction
year cv	2007	2007
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja0764052	10.1021/ja0764052
first author openalex	Vora	Vora

Citations

OpenAlex: 368
Scholar: none
DOI: 10.1021/ja0764052
OpenAlex: W2065989212

Match decisions

doi merged · 1.00 · Run 18

2007 Rhodium Catalyzed Enantioselective Desymmetrization of meso-3,5-Dimethyl Glutaric Anhydride: A General Strategy to syn- Deoxypolypropionate Synthons Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 245–246 · CV · published

245“Rhodium Catalyzed Enantioselective Desymmetrization of meso-3,5-Dimethyl Glutaric Anhydride: A General Strategy to syn-246Deoxypolypropionate Synthons”. M. J. Cook, T. Rovis*. J. Am. Chem. Soc. 2007, 129, 9302-9303.

Institution fields

Peer reviewed: yes
First author: Cook
Co-authors: M. J. Cook; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium Catalyzed Enantioselective Desymmetrization of meso-3,5-Dimethyl Glutaric Anhydride: A General Strategy to syn- Deoxypolypropionate Synthons	Rhodium-Catalyzed Enantioselective Desymmetrization of meso-3,5-Dimethyl Glutaric Anhydride: A General Strategy to syn-Deoxypolypropionate SynthonsRhodium‐Catalyzed Enantioselective Desymmetrization of meso‐3,5‐Dimethyl Glutaric Anhydride: A General Strategy to syn‐Deoxypolypropionate Synthons.
year cv	2007	20072007
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja073269s	10.1021/ja073269s10.1002/chin.200750091
first author openalex	Cook	CookCook

Also recorded as

W2951111334 (DOI 10.1002/chin.200750091) · same title · 2007 Rhodium‐Catalyzed Enantioselective Desymmetrization of meso‐3,5‐Dimethyl Glutaric Anhydride: A General Strategy to syn‐Deoxypolypropionate Synthons.

Citations

OpenAlex: 68
Scholar: none
DOI: 10.1021/ja073269s
OpenAlex: W2071462961

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1002/anie.200700816 for the synthesis of eupomatilones via desymmetrization.; The records share the same DOI 10.1021/ja073269s for the desymmetrization of meso-3,5-dimethyl glutaric anhydride.
doi merged · 1.00 · Run 18

2006 6,7-Dihydro-2-phenyl-5-(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride Encyclopedia of Reagents for Organic Synthesis chapter journal CV OA GS

CV span

lines 229–230 · CV · published

229“6,7-Dihydro-2-phenyl-5-(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride”. T. Rovis Electronic Encyclopedia of230Reagents for Organic Synthesis, 2006.

Institution fields

Peer reviewed: none
First author: Rovis
Co-authors: none
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	6,7-Dihydro-2-phenyl-5-(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride	6,7-Dihydro-2-phenyl-5-(phenylmethyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium Chloride
year cv	2006	2007
venue crossref	Electronic Encyclopedia of Reagents for Organic Synthesis	Encyclopedia of Reagents for Organic Synthesis	Encyclopedia of Reagents for Organic Synthesis
kind cv	chapter	chapter
DOI crossref	10.1002/047084289x.rn00736	10.1002/047084289x.rn00736
first author openalex	Rovis	Rovis

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/047084289x.rn00736
OpenAlex: W2177383614

Match decisions

doi merged · 1.00 · Run 18

2006 A Modular Approach to 2,3,4-Trisubstituted Tetrahydrofurans. Chemical Communications article journal CV OA GS

CV span

lines 217–218 · CV · published

217“A Modular Approach to 2,3,4-Trisubstituted Tetrahydrofurans.” C. G. Nasveschuk, N. T. Jui, T. Rovis*. Chem. Commun. 2006,2183119-3121.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; N. T. Jui; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Modular Approach to 2,3,4-Trisubstituted Tetrahydrofurans.	A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofuransA Modular Approach to the Synthesis of 2,3,4‐Trisubstituted Tetrahydrofurans.
year cv	2006	20062006
venue crossref	Chem. Commun.	Chemical CommunicationsChemInform	Chemical Communications
kind cv	article	articlearticle
DOI crossref	10.1039/b605438b	10.1039/b605438b10.1002/chin.200648120
first author openalex	Nasveschuk	NasveschukNasveschuk

Also recorded as

W2950875233 (DOI 10.1002/chin.200648120) · platform twin · 2006 A Modular Approach to the Synthesis of 2,3,4‐Trisubstituted Tetrahydrofurans.

Citations

OpenAlex: 17
Scholar: none
DOI: 10.1039/b605438b
OpenAlex: W2121929973

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2006 A Sakurai – Prins – Ritter Sequence for the Three-Component Diastereoselective Synthesis of 4-Amino Tetrahydropyrans. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 226–227 · CV · published

226“A Sakurai – Prins – Ritter Sequence for the Three-Component Diastereoselective Synthesis of 4-Amino Tetrahydropyrans.” O.227L. Epstein and T. Rovis*. J. Am. Chem. Soc. 2006, 128, 16480-16481.

Institution fields

Peer reviewed: yes
First author: Epstein
Co-authors: O. L. Epstein; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Sakurai – Prins – Ritter Sequence for the Three-Component Diastereoselective Synthesis of 4-Amino Tetrahydropyrans.	A Sakurai−Prins−Ritter Sequence for the Three-Component Diastereoselective Synthesis of 4-Amino TetrahydropyransA Sakurai—Prins—Ritter Sequence for the Three‐Component Diastereoselective Synthesis of 4‐Amino Tetrahydropyrans.
year cv	2006	20062007
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja066794k	10.1021/ja066794k10.1002/chin.200718131
first author openalex	Epstein	EpsteinEpstein

Also recorded as

W2952306040 (DOI 10.1002/chin.200718131) · same title · 2007 A Sakurai—Prins—Ritter Sequence for the Three‐Component Diastereoselective Synthesis of 4‐Amino Tetrahydropyrans.

Citations

OpenAlex: 83
Scholar: none
DOI: 10.1021/ja066794k
OpenAlex: W2020803997

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2006 Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter Reaction. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 211–212 · CV · published

211“Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter212Reaction.” Q. Liu and T. Rovis*. J. Am. Chem. Soc. 2006, 128, 2552-2553. (PMCID: PMC2701296)

Institution fields

Peer reviewed: yes
First author: Liu
Co-authors: Q. Liu; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter Reaction.	Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter ReactionAsymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter Reaction.
year cv	2006	20062006
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja058337u	10.1021/ja058337u10.1002/chin.200625127
first author openalex	Liu	LiuLiu

Also recorded as

W2951725946 (DOI 10.1002/chin.200625127) · same title · 2006

Citations

OpenAlex: 296
Scholar: none
DOI: 10.1021/ja058337u
OpenAlex: W1994230458

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2006 Enantioselective Formation of Quaternary Stereocenters using the Catalytic Intramolecular Stetter Reaction. Tetrahedron article journal CV OA GS

CV span

lines 214–215 · CV · published

214“Enantioselective Formation of Quaternary Stereocenters using the Catalytic Intramolecular Stetter Reaction.” J. L. Moore, M. S.215Kerr, T. Rovis*. Tetrahedron 2006, 62, 11477-11482.

Institution fields

Peer reviewed: yes
First author: Moore
Co-authors: J. L. Moore; M. S. Kerr; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Enantioselective Formation of Quaternary Stereocenters using the Catalytic Intramolecular Stetter Reaction.	Enantioselective Formation of Quaternary Stereocenters Using the Catalytic Intramolecular Stetter Reaction.Enantioselective formation of quaternary stereocenters using the catalytic intramolecular Stetter reaction
year cv	2006	20072006
venue crossref	Tetrahedron	ChemInformTetrahedron
kind cv	article	articlearticle
DOI crossref	10.1016/j.tet.2006.06.042	10.1002/chin.20071003210.1016/j.tet.2006.06.042
first author openalex	Moore	MooreMoore

Also recorded as

W1966592486 (DOI 10.1002/chin.200710032) · same title · 2007 Enantioselective Formation of Quaternary Stereocenters Using the Catalytic Intramolecular Stetter Reaction.

Citations

OpenAlex: 72
Scholar: none
DOI: 10.1016/j.tet.2006.06.042
OpenAlex: W2953077407

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2006 Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to the Total Synthesis of (+)-Lasubine II. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 223–224 · CV · published

223“Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to224the Total Synthesis of (+)-Lasubine II.” R. T. Yu and T. Rovis*. J. Am. Chem. Soc. 2006, 128, 12370-12371.

Institution fields

Peer reviewed: yes
First author: Yu
Co-authors: R. T. Yu; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to the Total Synthesis of (+)-Lasubine II.	Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to the Total Synthesis of (+)-Lasubine IIEnantioselective Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to the Total Synthesis of (+)‐Lasubine II.
year cv	2006	20062007
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja064868m	10.1021/ja064868m10.1002/chin.200705146
first author openalex	Yu	YuYu

Also recorded as

W2952240261 (DOI 10.1002/chin.200705146) · same title · 2007 Enantioselective Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Terminal Alkynes: Application to the Total Synthesis of (+)‐Lasubine II.

Citations

OpenAlex: 130
Scholar: none
DOI: 10.1021/ja064868m
OpenAlex: W2147579652

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja906641d for the [4+2+2] cycloaddition of dienyl isocyanates.

2006 Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 208–209 · CV · published

208“Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes.” R. T. Yu and T. Rovis*. J. Am. Chem. Soc.2092006, 128, 2782-2783.

Institution fields

Peer reviewed: yes
First author: Yu
Co-authors: R. T. Yu; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium-Catalyzed [2+2+2] Cycloaddition of Alkenyl Isocyanates and Alkynes.	Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and AlkynesRhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Alkynes.
year cv	2006	20062006
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja057803c	10.1021/ja057803c10.1002/chin.200629136
first author openalex	Yu	YuYu

Also recorded as

W2951159508 (DOI 10.1002/chin.200629136) · same title · 2006 Rhodium‐Catalyzed [2 + 2 + 2] Cycloaddition of Alkenyl Isocyanates and Alkynes.

Citations

OpenAlex: 96
Scholar: none
DOI: 10.1021/ja057803c
OpenAlex: W1971204412

Match decisions

gemini merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja906641d for the [4+2+2] cycloaddition of dienyl isocyanates.

2006 Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation. Organic Letters article journal CV OA GS

CV span

lines 220–222 · CV · published

220“Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation.” J. B. Johnson, R. T. Yu, P.221Fink, E. A. Bercot, T. Rovis*. Org. Lett. 2006, 8, 4307-4310.222

Institution fields

Peer reviewed: yes
First author: Johnson
Co-authors: J. B. Johnson; R. T. Yu; P. Fink; E. A. Bercot; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation.	Selective Substituent Transfer from Mixed Zinc Reagents in Ni‐Catalyzed Anhydride Alkylation.Selective Substituent Transfer from Mixed Zinc Reagents in Ni-Catalyzed Anhydride Alkylation
year cv	2006	20072006
venue crossref	Org. Lett.	ChemInformOrganic Letters	Organic Letters
kind cv	article	articlearticle
DOI crossref	10.1021/ol0616337	10.1002/chin.20070405210.1021/ol0616337
first author openalex	Johnson	JohnsonJohnson

Also recorded as

W2013034837 (DOI 10.1002/chin.200704052) · same title · 2007 Selective Substituent Transfer from Mixed Zinc Reagents in Ni‐Catalyzed Anhydride Alkylation.

Citations

OpenAlex: 56
Scholar: none
DOI: 10.1021/ol0616337
OpenAlex: W2951993232

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2006 Surveying approaches to the formation of carbon–carbon bonds between a pyran and an adjacent ring. Tetrahedron article journal CV OA GS

CV span

lines 205–206 · CV · published

205“Surveying approaches to the formation of carbon–carbon bonds between a pyran and an adjacent ring.” J. D. Frein and T.206Rovis*. Tetrahedron 2006, 62, 4573-4583. (PMCID: PMC1950123)

Institution fields

Peer reviewed: yes
First author: Frein
Co-authors: J. D. Frein; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Surveying approaches to the formation of carbon–carbon bonds between a pyran and an adjacent ring.	Surveying approaches to the formation of carbon–carbon bonds between a pyran and an adjacent ring
year cv	2006	2006
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/j.tet.2006.02.042	10.1016/j.tet.2006.02.042
first author openalex	Frein	Frein

Citations

OpenAlex: 18
Scholar: none
DOI: 10.1016/j.tet.2006.02.042
OpenAlex: W2062162708

Match decisions

doi merged · 1.00 · Run 18

2005 A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter Reaction. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 191–192 · CV · published

191“A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter Reaction.” J. Read de Alaniz and T. Rovis*. J. Am.192Chem. Soc. 2005, 127, 6284-6289.

Institution fields

Peer reviewed: yes
First author: Read de Alaniz
Co-authors: J. Read de Alaniz; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter Reaction.	A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter ReactionA Highly Enantio‐ and Diastereoselective Catalytic Intramolecular Stetter Reaction.
year cv	2005	20052005
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja0425132	10.1021/ja042513210.1002/chin.200538143
first author openalex	de Alaniz	de Alanizde Alaniz

Also recorded as

W2953149967 (DOI 10.1002/chin.200538143) · same title · 2005 A Highly Enantio‐ and Diastereoselective Catalytic Intramolecular Stetter Reaction.

Citations

OpenAlex: 250
Scholar: none
DOI: 10.1021/ja0425132
OpenAlex: W2051874798

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2005 An Efficient Synthesis of Achiral and Chiral 1,2,4-Triazolium Salts: Bench Stable Precursors for N-Heterocyclic Carbenes. The Journal of Organic Chemistry article journal CV OA GS

CV span

lines 197–198 · CV · published

197“An Efficient Synthesis of Achiral and Chiral 1,2,4-Triazolium Salts: Bench Stable Precursors for N-Heterocyclic Carbenes.” M.198S. Kerr, J. Read de Alaniz, T. Rovis*. J. Org. Chem. 2005, 70, 5725-5728. (PMCID: PMC2527449)

Institution fields

Peer reviewed: yes
First author: Kerr
Co-authors: M. S. Kerr; J. Read de Alaniz; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	An Efficient Synthesis of Achiral and Chiral 1,2,4-Triazolium Salts: Bench Stable Precursors for N-Heterocyclic Carbenes.	An Efficient Synthesis of Achiral and Chiral 1,2,4-Triazolium Salts: Bench Stable Precursors for N-Heterocyclic Carbenes
year cv	2005	2005
venue crossref	J. Org. Chem.	The Journal of Organic Chemistry	The Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1021/jo050645n	10.1021/jo050645n
first author openalex	Kerr	Kerr

Citations

OpenAlex: 268
Scholar: none
DOI: 10.1021/jo050645n
OpenAlex: W2048848046

Match decisions

doi merged · 1.00 · Run 18

2005 Anxiolytic Actions of Estrogen are mediated by Estrogen Receptor Beta. Endocrinology article journal CV OA GS

CV span

lines 182–183 · CV · published

182“Anxiolytic Actions of Estrogen are mediated by Estrogen Receptor Beta.” Trent D. Lund*, Tomislav Rovis, W. C. J. Chung,183Robert J. Handa*. Endocrinology, 2005, 146, 797-807.

Institution fields

Peer reviewed: yes
First author: Lund
Co-authors: Trent D. Lund; Tomislav Rovis; W. C. J. Chung; Robert J. Handa
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	Scholar
title cv	Anxiolytic Actions of Estrogen are mediated by Estrogen Receptor Beta.
year cv	2005
venue cv	Endocrinology
kind cv	article
first author cv	Lund

Citations

OpenAlex: none
Scholar: none

Match decisions

No decision recorded; a single record.

2005 Complementary Diastereoselective Reduction of Cyclic g-Keto Acids: Efficient Access to Trisubstituted g-Lactones ChemInform article journal CV OA GS

CV span

lines 179–180 · CV · published

179“Complementary Diastereoselective Reduction of Cyclic g-Keto Acids: Efficient Access to Trisubstituted g-Lactones” E. A.180Bercot, D. E. Kindrachuk, T. Rovis*. Org. Lett. 2005, 7, 107-110.

Institution fields

Peer reviewed: yes
First author: Bercot
Co-authors: E. A. Bercot; D. E. Kindrachuk; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Complementary Diastereoselective Reduction of Cyclic g-Keto Acids: Efficient Access to Trisubstituted g-Lactones	Complementary Diastereoselective Reduction of Cyclic γ‐Keto Acids: Efficient Access to Trisubstituted γ‐Lactones.Complementary Diastereoselective Reduction of Cyclic γ-Keto Acids: Efficient Access to Trisubsituted γ-Lactones
year cv	2005	20052004
venue crossref	Org. Lett.	ChemInformOrganic Letters	ChemInform
kind cv	article	articlearticle
DOI crossref	10.1002/chin.200517114	10.1002/chin.20051711410.1021/ol047821j
first author openalex	Bercot	BercotBercot

Also recorded as

W2953121823 (DOI 10.1021/ol047821j) · same title · 2004 Complementary Diastereoselective Reduction of Cyclic γ-Keto Acids: Efficient Access to Trisubsituted γ-Lactones

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/chin.200517114
OpenAlex: W2009087200

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2005 Enantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of a-Chloroesters. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 200–201 · CV · published

200“Enantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of a-Chloroesters.” N.201T. Reynolds and T. Rovis*. J. Am. Chem. Soc. 2005, 127, 16406-16407.

Institution fields

Peer reviewed: yes
First author: Reynolds
Co-authors: N. T. Reynolds; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of a-Chloroesters.	Enantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of α-ChloroestersEnantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of α‐Chloroesters.
year cv	2005	20052006
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja055918a	10.1021/ja055918a10.1002/chin.200615031
first author openalex	Reynolds	ReynoldsReynolds

Also recorded as

W2951280655 (DOI 10.1002/chin.200615031) · same title · 2006 Enantioselective Protonation of Catalytically Generated Chiral Enolates as an Approach to the Synthesis of α‐Chloroesters.

Citations

OpenAlex: 271
Scholar: none
DOI: 10.1021/ja055918a
OpenAlex: W1984792256

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2005 Highly Efficient Nickel-Catalyzed Cross-coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 176–177 · CV · published

176“Highly Efficient Nickel-Catalyzed Cross-coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents.” E. A.177Bercot and T. Rovis*. J. Am. Chem. Soc. 2005, 127, 247-254.

Institution fields

Peer reviewed: yes
First author: Bercot
Co-authors: E. A. Bercot; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Highly Efficient Nickel-Catalyzed Cross-coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents.	Highly Efficient Nickel-Catalyzed Cross-Coupling of Succinic and Glutaric Anhydrides with Organozinc ReagentsHighly Efficient Nickel‐Catalyzed Cross‐Coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents.
year cv	2005	20042005
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja044588b	10.1021/ja044588b10.1002/chin.200523101
first author openalex	Bercot	BercotBercot

Also recorded as

W2951951000 (DOI 10.1002/chin.200523101) · same title · 2005 Highly Efficient Nickel‐Catalyzed Cross‐Coupling of Succinic and Glutaric Anhydrides with Organozinc Reagents.

Citations

OpenAlex: 86
Scholar: none
DOI: 10.1021/ja044588b
OpenAlex: W2062981175

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2005 Regioselective Lewis Acid-Mediated [1,3] Rearrangement of Allylvinyl Ethers. Organic Letters article journal CV OA GS

CV span

lines 194–195 · CV · published

194“Regioselective Lewis Acid-Mediated [1,3] Rearrangement of Allylvinyl Ethers.” C. G. Nasveschuk and T. Rovis*. Org. Lett.1952005, 7, 2173-2176.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Regioselective Lewis Acid-Mediated [1,3] Rearrangement of Allylvinyl Ethers.	Regioselective Lewis Acid-Mediated [1,3] Rearrangement of Allylvinyl EthersRegioselective Lewis Acid Mediated [1,3] Rearrangement of Allylvinyl Ethers.
year cv	2005	20052005
venue crossref	Org. Lett.	Organic LettersChemInform	Organic Letters
kind cv	article	articlearticle
DOI crossref	10.1021/ol0505151	10.1021/ol050515110.1002/chin.200542046
first author openalex	Nasveschuk	NasveschukNasveschuk

Also recorded as

W2950431109 (DOI 10.1002/chin.200542046) · same title · 2005 Regioselective Lewis Acid Mediated [1,3] Rearrangement of Allylvinyl Ethers.

Citations

OpenAlex: 37
Scholar: none
DOI: 10.1021/ol0505151
OpenAlex: W2074373402

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2005 Stereoselective Lewis Acid-Mediated [1,3] Ring Contraction of 2,5-Dihydrooxepins as a Route to Polysubstituted Cyclopentanes. Angewandte Chemie International Edition article journal CV OA GS

CV span

lines 188–189 · CV · published

188“Stereoselective Lewis Acid-Mediated [1,3] Ring Contraction of 2,5-Dihydrooxepins as a Route to Polysubstituted189Cyclopentanes.” C. G. Nasveschuk and T. Rovis*. Angew. Chem. Int. Edit. 2005, 44, 3264-3267.

Institution fields

Peer reviewed: yes
First author: Nasveschuk
Co-authors: C. G. Nasveschuk; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Stereoselective Lewis Acid-Mediated [1,3] Ring Contraction of 2,5-Dihydrooxepins as a Route to Polysubstituted Cyclopentanes.	Stereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5‐Dihydrooxepins as a Route to Polysubstituted CyclopentenesStereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5‐Dihydrooxepins as a Route to Polysubstituted Cyclopentenes.Stereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5‐Dihydrooxepins as a Route to Polysubstituted Cyclopentenes
year cv	2005	200520052005
venue crossref	Angew. Chem. Int. Edit.	Angewandte Chemie International EditionChemInformAngewandte Chemie	Angewandte Chemie International Edition
kind cv	article	articlearticlearticle
DOI crossref	10.1002/anie.200500088	10.1002/anie.20050008810.1002/chin.20053807910.1002/ange.200500088
first author openalex	Nasveschuk	NasveschukNasveschukNasveschuk

Also recorded as

W2949618395 (DOI 10.1002/chin.200538079) · platform twin · 2005 Stereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5‐Dihydrooxepins as a Route to Polysubstituted Cyclopentenes.
W4247873470 (DOI 10.1002/ange.200500088) · platform twin · 2005 Stereoselective Lewis Acid Mediated [1,3] Ring Contraction of 2,5‐Dihydrooxepins as a Route to Polysubstituted Cyclopentenes

Citations

OpenAlex: 43
Scholar: none
DOI: 10.1002/anie.200500088
OpenAlex: W2133448165

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2005 The Effect of Preexisting Stereocenters in the Intramolecular Asymmetric Stetter Reaction. Tetrahedron article journal CV OA GS

CV span

lines 185–186 · CV · published

185“The Effect of Preexisting Stereocenters in the Intramolecular Asymmetric Stetter Reaction.” N. T. Reynolds and T. Rovis*.186Tetrahedron, 2005, 61, 6368-6378.

Institution fields

Peer reviewed: yes
First author: Reynolds
Co-authors: N. T. Reynolds; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	The Effect of Preexisting Stereocenters in the Intramolecular Asymmetric Stetter Reaction.	The effect of pre-existing stereocenters in the intramolecular asymmetric Stetter reaction
year cv	2005	2005
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/j.tet.2005.03.121	10.1016/j.tet.2005.03.121
first author openalex	Reynolds	Reynolds

Citations

OpenAlex: 60
Scholar: none
DOI: 10.1016/j.tet.2005.03.121
OpenAlex: W2003000616

Match decisions

doi merged · 1.00 · Run 18

2004 A Palladium Catalyzed Enantioselective Alkylative Desymmetrizationo of meso-Succinic Anhydrides. ChemInform article journal CV OA GS

CV span

lines 165–166 · CV · published

165“A Palladium Catalyzed Enantioselective Alkylative Desymmetrizationo of meso-Succinic Anhydrides.” E. A. Bercot and T.166Rovis*. J. Am. Chem. Soc. 2004, 126, 10248-10249.

Institution fields

Peer reviewed: yes
First author: Bercot
Co-authors: E. A. Bercot; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Palladium Catalyzed Enantioselective Alkylative Desymmetrizationo of meso-Succinic Anhydrides.	A Palladium-Catalyzed Enantioselective Alkylative Desymmetrization of meso-Succinic AnhydridesA Palladium‐Catalyzed Enantioselective Alkylative Desymmetrization of meso‐Succinic Anhydrides.
year cv	2004	20042004
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	ChemInform
kind cv	article	articlearticle
DOI crossref	10.1002/chin.200451030	10.1021/ja046528b10.1002/chin.200451030
first author openalex	Bercot	BercotBercot

Also recorded as

W2041614076 (DOI 10.1021/ja046528b) · platform twin · 2004 A Palladium-Catalyzed Enantioselective Alkylative Desymmetrization of meso-Succinic Anhydrides

Citations

OpenAlex: 0
Scholar: none
DOI: 10.1002/chin.200451030
OpenAlex: W2950145663

Match decisions

gemini merged · 0.95 · Run 18 The records match on ChemInform and journal reference for the alkylative desymmetrization of succinic anhydrides.

2004 A Unique Catalyst Effects the Rapid Room Temperature Cross-coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides and Thioesters. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 171–172 · CV · published

171“A Unique Catalyst Effects the Rapid Room Temperature Cross-coupling of Organozinc Reagents with Carboxylic Acid172Fluorides, Chlorides, Anhydrides and Thioesters.” Y. Zhang and T. Rovis*. J. Am. Chem. Soc. 2004, 126, 15964-15965.

Institution fields

Peer reviewed: yes
First author: Zhang
Co-authors: Y. Zhang; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Unique Catalyst Effects the Rapid Room Temperature Cross-coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides and Thioesters.	A Unique Catalyst Effects the Rapid Room-Temperature Cross-Coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides, and ThioestersA Unique Catalyst Effects the Rapid Room‐Temperature Cross‐Coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides, and Thioesters.
year cv	2004	20042005
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja044113k	10.1021/ja044113k10.1002/chin.200515074
first author openalex	Zhang	ZhangZhang

Also recorded as

W2949232829 (DOI 10.1002/chin.200515074) · same title · 2005 A Unique Catalyst Effects the Rapid Room‐Temperature Cross‐Coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides, and Thioesters.

Citations

OpenAlex: 225
Scholar: none
DOI: 10.1021/ja044113k
OpenAlex: W2029577964

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2004 Conversion of a-Haloaldehydes into Acylating Agents Catalyzed by Nucleophilic Carbenes. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 162–163 · CV · published

162“Conversion of a-Haloaldehydes into Acylating Agents Catalyzed by Nucleophilic Carbenes.” N. T. Reynolds, J. Read de163Alaniz, T. Rovis*. J. Am. Chem. Soc. 2004, 126, 9518-9519.

Institution fields

Peer reviewed: yes
First author: Reynolds
Co-authors: N. T. Reynolds; J. Read de Alaniz; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Conversion of a-Haloaldehydes into Acylating Agents Catalyzed by Nucleophilic Carbenes.	Conversion of α-Haloaldehydes into Acylating Agents by an Internal Redox Reaction Catalyzed by Nucleophilic CarbenesConversion of α‐Haloaldehydes into Acylating Agents by an Internal Redox Reaction Catalyzed by Nucleophilic Carbenes.
year cv	2004	20042004
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja046991o	10.1021/ja046991o10.1002/chin.200448051
first author openalex	Reynolds	ReynoldsReynolds

Also recorded as

W2952334172 (DOI 10.1002/chin.200448051) · platform twin · 2004 Conversion of α‐Haloaldehydes into Acylating Agents by an Internal Redox Reaction Catalyzed by Nucleophilic Carbenes.

Citations

OpenAlex: 383
Scholar: none
DOI: 10.1021/ja046991o
OpenAlex: W2041800381

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2004 Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Enantioselective Stetter Reaction. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 159–160 · CV · published

159“Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Enantioselective Stetter Reaction.” M. S. Kerr and T.160Rovis*. J. Am. Chem. Soc. 2004, 126, 8876-8877.

Institution fields

Peer reviewed: yes
First author: Kerr
Co-authors: M. S. Kerr; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Enantioselective Stetter Reaction.	Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter ReactionEnantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter Reaction.
year cv	2004	20042004
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja047644h	10.1021/ja047644h10.1002/chin.200445032
first author openalex	Kerr	KerrKerr

Also recorded as

W2949679712 (DOI 10.1002/chin.200445032) · platform twin · 2004 Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter Reaction.

Citations

OpenAlex: 321
Scholar: none
DOI: 10.1021/ja047644h
OpenAlex: W1998647682

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: platform_twin

2004 Recent Advances in Catalytic Asymmetric Desymmetrization Reactions. New Frontiers in Asymmetric Catalysis chapter CV OA GS

CV span

lines 168–169 · CV · published

168“Recent Advances in Catalytic Asymmetric Desymmetrization Reactions.” T. Rovis. Invited Chapter in New Frontiers in169Asymmetric Catalysis, Koichi Mikami and Mark Lautens, eds.

Institution fields

Peer reviewed: none
First author: Rovis
Co-authors: none
Subfield: other
Method: none
Invited: yes
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Recent Advances in Catalytic Asymmetric Desymmetrization Reactions.	Recent Advances in Catalytic Asymmetric Desymmetrization Reactions
year cv	2004	2006
venue cv	New Frontiers in Asymmetric Catalysis
kind cv	chapter	other
DOI openalex		10.1002/9780470098004.ch10
first author cv	Rovis	Rovis

Also recorded as

W1501854153 (DOI 10.1002/9780470098004.ch10) · same title · 2006 Recent Advances in Catalytic Asymmetric Desymmetrization Reactions

Citations

OpenAlex: 46
Scholar: none
DOI: 10.1002/9780470098004.ch10

Match decisions

classified merged · Run 18 resolved by the OpenAlex classification: same_title

2004 The Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters. Organic Letters article journal CV OA GS

CV span

lines 156–157 · CV · published

156“The Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters.” Y. Zhang and T. Rovis*. Org. Lett. 2004,1576, 1877-1879.

Institution fields

Peer reviewed: yes
First author: Zhang
Co-authors: Y. Zhang; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	The Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters.	Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters.Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters
year cv	2004	20042004
venue crossref	Org. Lett.	ChemInformOrganic Letters	Organic Letters
kind cv	article	articlearticle
DOI crossref	10.1021/ol049333h	10.1002/chin.20044005910.1021/ol049333h
first author openalex	Zhang	ZhangZhang

Also recorded as

W2094572288 (DOI 10.1002/chin.200440059) · same title · 2004 Use of Acid Fluorides Increases the Scope of the Reductive Acylation of Esters.

Citations

OpenAlex: 27
Scholar: none
DOI: 10.1021/ol049333h
OpenAlex: W2953119282

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2003 1,3-Polyol Arrays via the Stereoselective Rearrangement of Vinyl Acetals. Tetrahedron article journal CV OA GS

CV span

lines 148–149 · CV · published

148“1,3-Polyol Arrays via the Stereoselective Rearrangement of Vinyl Acetals.” Y. Zhang and T. Rovis*. Tetrahedron 2003, 59,1498979-8987.

Institution fields

Peer reviewed: yes
First author: Zhang
Co-authors: Y. Zhang; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	1,3-Polyol Arrays via the Stereoselective Rearrangement of Vinyl Acetals.	1,3-Polyol arrays via the stereoselective rearrangement of vinyl acetals
year cv	2003	2003
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/j.tet.2003.03.004	10.1016/j.tet.2003.03.004
first author openalex	Zhang	Zhang

Citations

OpenAlex: 17
Scholar: none
DOI: 10.1016/j.tet.2003.03.004
OpenAlex: W2070495564

Match decisions

doi merged · 1.00 · Run 18

2003 Decarbonylative Cross-coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3-Carbon in the Cross-coupling Event. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 142–143 · CV · published

142“Decarbonylative Cross-coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3-Carbon in the Cross-coupling143Event.” E. M. O’Brien, E. A. Bercot and T. Rovis*. J. Am. Chem. Soc. 2003, 125, 10498.

Institution fields

Peer reviewed: yes
First author: O’Brien
Co-authors: E. M. O’Brien; E. A. Bercot; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Decarbonylative Cross-coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3-Carbon in the Cross-coupling Event.	Decarbonylative Cross-Coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3 Carbon in the Cross-Coupling EventDecarbonylative Cross‐Coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3 Carbon in the Cross‐Coupling Event.
year cv	2003	20032003
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja036290b	10.1021/ja036290b10.1002/chin.200402060
first author openalex	O’Brien	O’BrienO’Brien

Also recorded as

W2949190830 (DOI 10.1002/chin.200402060) · same title · 2003 Decarbonylative Cross‐Coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3 Carbon in the Cross‐Coupling Event.

Citations

OpenAlex: 122
Scholar: none
DOI: 10.1021/ja036290b
OpenAlex: W2067124483

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2003 Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction. Synlett article journal CV OA GS

CV span

lines 151–152 · CV · published

151“Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction.” M. S. Kerr and T. Rovis*. Synlett 2003,1521934-1936.

Institution fields

Peer reviewed: yes
First author: Kerr
Co-authors: M. S. Kerr; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction.	Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction.Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction
year cv	2003	20042003
venue crossref	Synlett	ChemInformSynlett
kind cv	article	articlearticle
DOI crossref	10.1055/s-2003-41458	10.1002/chin.20040713110.1055/s-2003-41458
first author openalex	Kerr	KerrRovis

Also recorded as

W2036525227 (DOI 10.1002/chin.200407131) · same title · 2004

Citations

OpenAlex: 12
Scholar: none
DOI: 10.1055/s-2003-41458
OpenAlex: W2952097205

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2003 Metal and Non-metal Catalysts for Carbon-carbon Bond-Forming Reactions Leading to Desymmetrized 1,4-dicarbonyl Compounds. ChemInform article journal CV OA GS

CV span

lines 145–146 · CV · published

145“Metal and Non-metal Catalysts for Carbon-carbon Bond-Forming Reactions Leading to Desymmetrized 1,4-dicarbonyl146Compounds.” T. Rovis, Chemtracts: Org. 2003, 16, 542.

Institution fields

Peer reviewed: yes
First author: Rovis
Co-authors: none
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Metal and Non-metal Catalysts for Carbon-carbon Bond-Forming Reactions Leading to Desymmetrized 1,4-dicarbonyl Compounds.	Metal and Nonmetal Catalysts for Carbon——Carbon Bond‐Forming Reactions Leading to Desymmetrized 1,4‐Dicarbonyl Compounds
year cv	2003	2004
venue crossref	Chemtracts: Org.	ChemInform	ChemInform
kind cv	article	article
DOI crossref	10.1002/chin.200427262	10.1002/chin.200427262
first author openalex	Rovis	Rovis

Citations

OpenAlex: 1
Scholar: none
DOI: 10.1002/chin.200427262
OpenAlex: W2006708944

Match decisions

doi merged · 1.00 · Run 18

2002 A Highly Enantioselective Catalytic Intramolecular Stetter Reaction. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 137–138 · CV · published

137“A Highly Enantioselective Catalytic Intramolecular Stetter Reaction.” M. S. Kerr, J. Read de Alaniz and T. Rovis*. J. Am.138Chem. Soc. 2002, 124, 10298.

Institution fields

Peer reviewed: yes
First author: Kerr
Co-authors: M. S. Kerr; J. Read de Alaniz; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Highly Enantioselective Catalytic Intramolecular Stetter Reaction.	A Highly Enantioselective Catalytic Intramolecular Stetter ReactionA Highly Enantioselective Catalytic Intramolecular Stetter Reaction.
year cv	2002	20022003
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical SocietyChemInform	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja027411v	10.1021/ja027411v10.1002/chin.200301029
first author openalex	Kerr	KerrKerr

Also recorded as

W2951864214 (DOI 10.1002/chin.200301029) · same title · 2003

Citations

OpenAlex: 501
Scholar: none
DOI: 10.1021/ja027411v
OpenAlex: W2062406334

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2002 A Mild and Efficient Catalytic Alkylative Monofunctionalization of Cyclic Anhydrides. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 131–132 · CV · published

131“A Mild and Efficient Catalytic Alkylative Monofunctionalization of Cyclic Anhydrides.” E. A. Bercot and T. Rovis*. J. Am.132Chem. Soc. 2002, 124, 174.

Institution fields

Peer reviewed: yes
First author: Bercot
Co-authors: E. A. Bercot; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A Mild and Efficient Catalytic Alkylative Monofunctionalization of Cyclic Anhydrides.	A Mild and Efficient Catalytic Alkylative Monofunctionalization of Cyclic Anhydrides
year cv	2002	2001
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja017086w	10.1021/ja017086w
first author openalex	Bercot	Bercot

Citations

OpenAlex: 106
Scholar: none
DOI: 10.1021/ja017086w
OpenAlex: W2013149966

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja017086w for the catalytic alkylative monofunctionalization.
doi merged · 1.00 · Run 18

2002 Stereoretentive O-to-C Rearrangement of Vinyl Acetals. Solvent Cage Effects as a Stereocontrol Element. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 134–135 · CV · published

134“Stereoretentive O-to-C Rearrangement of Vinyl Acetals. Solvent Cage Effects as a Stereocontrol Element.” Y. Zhang, N. T.135Reynolds, K. Manju and T. Rovis*. J. Am. Chem. Soc. 2002, 124, 9720.

Institution fields

Peer reviewed: yes
First author: Zhang
Co-authors: Y. Zhang; N. T. Reynolds; K. Manju; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Stereoretentive O-to-C Rearrangement of Vinyl Acetals. Solvent Cage Effects as a Stereocontrol Element.	Stereoretentive O‐ to ‐C Rearrangement of Vinyl Acetals: Solvent Cage Effects as a Stereocontrol Element.Stereoretentive O-to-C Rearrangement of Vinyl Acetals: Solvent Cage Effects as a Stereocontrol Element
year cv	2002	20022002
venue crossref	J. Am. Chem. Soc.	ChemInformJournal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	articlearticle
DOI crossref	10.1021/ja026972j	10.1002/chin.20025105010.1021/ja026972j
first author openalex	Zhang	ZhangZhang

Also recorded as

W2043774339 (DOI 10.1002/chin.200251050) · same title · 2002 Stereoretentive O‐ to ‐C Rearrangement of Vinyl Acetals: Solvent Cage Effects as a Stereocontrol Element.

Citations

OpenAlex: 44
Scholar: none
DOI: 10.1021/ja026972j
OpenAlex: W2949963400

Match decisions

classified merged · 0.99 · Run 18 resolved by the OpenAlex classification: same_title

2001 Highly Enantioselective Syntheses of Homopropargylic Alcohols and Dihydrofurans Catalyzed by a Bis(oxazolinyl)pyridine – Scandium Triflate Complex. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 126–127 · CV · published

126“Highly Enantioselective Syntheses of Homopropargylic Alcohols and Dihydrofurans Catalyzed by a Bis(oxazolinyl)pyridine –127Scandium Triflate Complex.” D. A. Evans*, Z. K. Sweeney, T. Rovis, J. S. Tedrow, J. Am. Chem. Soc. 2001, 123, 12095.

Institution fields

Peer reviewed: yes
First author: Evans
Co-authors: D. A. Evans; Z. K. Sweeney; T. Rovis; J. S. Tedrow
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Highly Enantioselective Syntheses of Homopropargylic Alcohols and Dihydrofurans Catalyzed by a Bis(oxazolinyl)pyridine – Scandium Triflate Complex.	Highly Enantioselective Syntheses of Homopropargylic Alcohols and Dihydrofurans Catalyzed by a Bis(oxazolinyl)pyridine−Scandium Triflate Complex
year cv	2001	2001
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja011983i	10.1021/ja011983i
first author openalex	Evans	Evans

Citations

OpenAlex: 203
Scholar: none
DOI: 10.1021/ja011983i
OpenAlex: W2015734041

Match decisions

doi merged · 1.00 · Run 18

2001 Mechanistic and Structural Investigations in Asymmetric Cu(I) and Cu(II) Catalyzed Reactions. Progress in Inorganic Chemistry article CV OA GS

CV span

lines 120–121 · CV · published

120"Mechanistic and Structural Investigations in Asymmetric Cu(I) and Cu(II) Catalyzed Reactions." T. Rovis* and D. A. Evans,121Prog. Inorg. Chem. 2001, 50, 1.

Institution fields

Peer reviewed: yes
First author: Rovis
Co-authors: T. Rovis; D. A. Evans
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Mechanistic and Structural Investigations in Asymmetric Cu(I) and Cu(II) Catalyzed Reactions.	Structural and Mechanistic Investigations in Asymmetric Copper(I) and Copper(II) Catalyzed Reactions
year cv	2001	2001
venue crossref	Prog. Inorg. Chem.	Progress in inorganic chemistry	Progress in Inorganic Chemistry
kind cv	article	other
DOI crossref	10.1002/0471227110.ch1	10.1002/0471227110.ch1
first author openalex	Rovis	Rovis

Citations

OpenAlex: 64
Scholar: none
DOI: 10.1002/0471227110.ch1
OpenAlex: W2161137679

Match decisions

doi merged · 1.00 · Run 18

2001 Rhodium-Catalysed Asymmetric Ring Opening of Oxabicyclic Alkenes with Heteroatom Nucleophiles. Journal of Organometallic Chemistry article journal CV OA GS needs review

CV span

lines 123–124 · CV · published

123"Rhodium-Catalysed Asymmetric Ring Opening of Oxabicyclic Alkenes with Heteroatom Nucleophiles." M. Lautens*, K.124Fagnou, M. Taylor, T. Rovis. J. Organomet. Chem. 2001, 624, 259.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; K. Fagnou; M. Taylor; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium-Catalysed Asymmetric Ring Opening of Oxabicyclic Alkenes with Heteroatom Nucleophiles.	Rhodium-catalysed asymmetric ring opening of oxabicyclic alkenes with heteroatom nucleophiles
year cv	2001	2001
venue crossref	J. Organomet. Chem.	Journal of Organometallic Chemistry	Journal of Organometallic Chemistry
kind cv	article	article
DOI crossref	10.1016/s0022-328x(00)00904-9	10.1016/s0022-328x(00)00904-9
first author openalex	Lautens	Lautens

Citations

OpenAlex: 82
Scholar: none
DOI: 10.1016/s0022-328x(00)00904-9
OpenAlex: W2055445049

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1016/s0022-328x(00)00904-9 for the rhodium-catalysed asymmetric ring opening.
doi merged · 1.00 · Run 18

2000 Enantioselective Mukaiyama Michael Reactions of Alkylidene Malonates. C2-Symmetric Bis(oxazoline) Copper (II) Complexes in the Synthesis of Chiral, Differentiated Glutarate Esters. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 114–116 · CV · published

114“Enantioselective Mukaiyama Michael Reactions of Alkylidene Malonates. C2-Symmetric Bis(oxazoline) Copper (II)115Complexes in the Synthesis of Chiral, Differentiated Glutarate Esters.” D. A. Evans*, T. Rovis, M. C. Kozlowski, C. W.116Downey, J. S. Tedrow, J. Am. Chem. Soc. 2000, 122, 9134.

Institution fields

Peer reviewed: yes
First author: Evans
Co-authors: D. A. Evans; T. Rovis; M. C. Kozlowski; C. W. Downey; J. S. Tedrow
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Enantioselective Mukaiyama Michael Reactions of Alkylidene Malonates. C2-Symmetric Bis(oxazoline) Copper (II) Complexes in the Synthesis of Chiral, Differentiated Glutarate Esters.	Enantioselective Lewis Acid Catalyzed Michael Reactions of Alkylidene Malonates. Catalysis byC2-Symmetric Bis(oxazoline) Copper(II) Complexes in the Synthesis of Chiral, Differentiated Glutarate Esters
year cv	2000	2000
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja002246+	10.1021/ja002246+
first author openalex	Evans	Evans

Citations

OpenAlex: 137
Scholar: none
DOI: 10.1021/ja002246+
OpenAlex: W2001458251

Match decisions

doi merged · 1.00 · Run 18

2000 Rhodium Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon- Heteroatom Bond Forming Process. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 111–112 · CV · published

111“Rhodium Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon-112Heteroatom Bond Forming Process.” M. Lautens*, K. Fagnou, T. Rovis, J. Am. Chem. Soc. 2000, 122, 5650.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; K. Fagnou; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Rhodium Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon- Heteroatom Bond Forming Process.	Rhodium-Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon−Heteroatom Bond Forming Process
year cv	2000	2000
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja000134c	10.1021/ja000134c
first author openalex	Lautens	Lautens

Citations

OpenAlex: 160
Scholar: none
DOI: 10.1021/ja000134c
OpenAlex: W2952929440

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja000134c for the rhodium-catalyzed alcoholysis and aminolysis.
doi merged · 1.00 · Run 18

1999 C2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Michael Addition of Silylketene Acetals to Alkylidene Malonates. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 103–104 · CV · published

103"C2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Michael Addition of Silylketene Acetals to104Alkylidene Malonates." D. A. Evans*, T. Rovis, M. C. Kozlowski, J. S. Tedrow, J. Am. Chem. Soc. 1999, 121, 1994.

Institution fields

Peer reviewed: yes
First author: Evans
Co-authors: D. A. Evans; T. Rovis; M. C. Kozlowski; J. S. Tedrow
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	C2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Michael Addition of Silylketene Acetals to Alkylidene Malonates.	C2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Michael Addition of Silylketene Acetals to Alkylidene Malonates
year cv	1999	1999
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja983864h	10.1021/ja983864h
first author openalex	Evans	Evans

Citations

OpenAlex: 170
Scholar: none
DOI: 10.1021/ja983864h
OpenAlex: W2072187289

Match decisions

doi merged · 1.00 · Run 18

1999 Chiral Copper(II) Complexes as Lewis Acids for Catalyzed Cycloaddition, Carbonyl Addition, and Conjugate Addition Reactions. Pure and Applied Chemistry article journal CV OA GS

CV span

lines 106–107 · CV · published

106"Chiral Copper(II) Complexes as Lewis Acids for Catalyzed Cycloaddition, Carbonyl Addition, and Conjugate Addition107Reactions." D. A. Evans*, T. Rovis, J. S. Johnson, Pure & Appl. Chem. 1999, 71, 1407.

Institution fields

Peer reviewed: yes
First author: Evans
Co-authors: D. A. Evans; T. Rovis; J. S. Johnson
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Chiral Copper(II) Complexes as Lewis Acids for Catalyzed Cycloaddition, Carbonyl Addition, and Conjugate Addition Reactions.	Chiral copper (ii) complexes as Lewis acids for catalyzed cycloaddition, carbonyl addition, and conjugate addition reactions
year cv	1999	1999
venue crossref	Pure & Appl. Chem.	Pure and Applied Chemistry	Pure and Applied Chemistry
kind cv	article	article
DOI crossref	10.1351/pac199971081407	10.1351/pac199971081407
first author openalex	Evans	Evans

Citations

OpenAlex: 105
Scholar: none
DOI: 10.1351/pac199971081407
OpenAlex: W2096117687

Match decisions

doi merged · 1.00 · Run 18

1999 Enantioselective Hydroalumination. Comprehensive Asymmetric Catalysis chapter CV OA GS

CV span

lines 97–98 · CV · published

97"Enantioselective Hydroalumination." M. Lautens* and T. Rovis, Comprehensive Asymmetric Catalysis ed. by E. N. Jacobsen, A.98Pfaltz, H. Yamamoto. 1999, 337.

Institution fields

Peer reviewed: none
First author: Lautens
Co-authors: M. Lautens; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	Scholar
title cv	Enantioselective Hydroalumination.
year cv	1999
venue cv	Comprehensive Asymmetric Catalysis
kind cv	chapter
first author cv	Lautens

Citations

OpenAlex: none
Scholar: none

Match decisions

No decision recorded; a single record.

1999 Selective Functionalization of 1,2-Dihydronaphthalenols Leads to a Concise, Stereoselective Synthesis of Sertraline. Tetrahedron article journal CV OA GS needs review

CV span

lines 100–101 · CV · published

100“Selective Functionalization of 1,2-Dihydronaphthalenols Leads to a Concise, Stereoselective Synthesis of Sertraline.” M.101Lautens* and T. Rovis, Tetrahedron 1999, 55, 8967.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Selective Functionalization of 1,2-Dihydronaphthalenols Leads to a Concise, Stereoselective Synthesis of Sertraline.	Selective functionalization of 1,2-dihydronaphthalenols leads to a concise, stereoselective synthesis of sertraline
year cv	1999	1999
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/s0040-4020(99)00456-1	10.1016/s0040-4020(99)00456-1
first author openalex	Lautens	Lautens

Citations

OpenAlex: 87
Scholar: none
DOI: 10.1016/s0040-4020(99)00456-1
OpenAlex: W2083729647

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1016/s0040-4020(99)00456-1 for the selective functionalization paper.
doi merged · 1.00 · Run 18

1998 Metal Catalyzed Hydrometalations and their Applications in Synthesis. Pure and Applied Chemistry article journal CV OA GS

CV span

lines 92–93 · CV · published

92"Metal Catalyzed Hydrometalations and their Applications in Synthesis." M. Lautens*, T. Rovis, N. D. Smith, D. Ostrovsky,93Pure & Appl. Chem. 1998,70, 1059.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; T. Rovis; N. D. Smith; D. Ostrovsky
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Metal Catalyzed Hydrometalations and their Applications in Synthesis.	Metal catalyzed hydrometalations and their applications in synthesis
year cv	1998	1998
venue crossref	Pure & Appl. Chem.	Pure and Applied Chemistry	Pure and Applied Chemistry
kind cv	article	article
DOI crossref	10.1351/pac199870051059	10.1351/pac199870051059
first author openalex	Lautens	Lautens

Citations

OpenAlex: 28
Scholar: none
DOI: 10.1351/pac199870051059
OpenAlex: W2157870618

Match decisions

doi merged · 1.00 · Run 18

1998 Scope of the Nickel Catalyzed Asymmetric Reductive Ring Opening Reaction. Synthesis of Enantiomerically Enriched Cyclohexenols. Tetrahedron article journal CV OA GS needs review

CV span

lines 89–90 · CV · published

89“Scope of the Nickel Catalyzed Asymmetric Reductive Ring Opening Reaction. Synthesis of Enantiomerically Enriched90Cyclohexenols.” M. Lautens* and T. Rovis, Tetrahedron 1998, 54, 1107.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex
title cv	Scope of the Nickel Catalyzed Asymmetric Reductive Ring Opening Reaction. Synthesis of Enantiomerically Enriched Cyclohexenols.	Scope of the nickel catalyzed asymmetric reductive ring opening reaction. Synthesis of enantiomerically enriched cyclohexenols
year cv	1998	1998
venue crossref	Tetrahedron	Tetrahedron
kind cv	article	article
DOI crossref	10.1016/s0040-4020(97)10211-3	10.1016/s0040-4020(97)10211-3
first author openalex	Lautens	Lautens

Citations

OpenAlex: 46
Scholar: none
DOI: 10.1016/s0040-4020(97)10211-3
OpenAlex: W1981788417

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1016/s0040-4020(97)10211-3 for the nickel catalyzed asymmetric reductive ring opening.
doi merged · 1.00 · Run 18

1997 A General Strategy Toward the Tetrahydronaphthalene Skeleton. An Expedient Total Synthesis of Sertraline. The Journal of Organic Chemistry article journal CV OA GS needs review

CV span

lines 81–82 · CV · published

81"A General Strategy Toward the Tetrahydronaphthalene Skeleton. An Expedient Total Synthesis of Sertraline." M. Lautens* and82T. Rovis, J. Org. Chem. 1997, 62, 5246.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A General Strategy Toward the Tetrahydronaphthalene Skeleton. An Expedient Total Synthesis of Sertraline.	General Strategy toward the Tetrahydronaphthalene Skeleton. An Expedient Total Synthesis of Sertraline
year cv	1997	1997
venue crossref	J. Org. Chem.	The Journal of Organic Chemistry	The Journal of Organic Chemistry
kind cv	article	article
DOI crossref	10.1021/jo971115x	10.1021/jo971115x
first author openalex	Lautens	Lautens

Citations

OpenAlex: 95
Scholar: none
DOI: 10.1021/jo971115x
OpenAlex: W2170080608

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/jo971115x for the total synthesis of sertraline.
doi merged · 1.00 · Run 18

1997 A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes. Journal of the American Chemical Society article journal CV OA GS

CV span

lines 84–85 · CV · published

84"A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring85Opening of [3.2.1] Oxabicycloalkenes." M. Lautens* and T. Rovis, J. Am. Chem. Soc. 1997, 119, 11090.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes.	A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes
year cv	1997	1997
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja971770m	10.1021/ja971770m
first author openalex	Lautens	Lautens

Citations

OpenAlex: 82
Scholar: none
DOI: 10.1021/ja971770m
OpenAlex: W2950764636

Match decisions

doi merged · 1.00 · Run 18

1995 Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity. Journal of the American Chemical Society article journal CV OA GS needs review

CV span

lines 76–77 · CV · published

76"Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity." M.77Lautens*, P. Chiu, S. Ma, T. Rovis, J. Am. Chem. Soc. 1995, 117, 532.

Institution fields

Peer reviewed: yes
First author: Lautens
Co-authors: M. Lautens; P. Chiu; S. Ma; T. Rovis
Subfield: other
Method: none
Invited: none
Publisher: none
Reprint or translation: none

Fields by source

Field	CV	OpenAlex	CrossRef
title cv	Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity.	Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity
year cv	1995	1995
venue crossref	J. Am. Chem. Soc.	Journal of the American Chemical Society	Journal of the American Chemical Society
kind cv	article	article
DOI crossref	10.1021/ja00106a062	10.1021/ja00106a062
first author openalex	Lautens	Lautens

Citations

OpenAlex: 110
Scholar: none
DOI: 10.1021/ja00106a062
OpenAlex: W2952237283

Match decisions

passthrough_guard not merged · 0.99 · doi_conflict · Run 18 The records share the same DOI 10.1021/ja00106a062 for the nickel-catalyzed hydroalumination.
doi merged · 1.00 · Run 18

Citations received by year

Publications

Positions

Entries needing review

Entries dropped by a reviewer

Title	Organization	Years	Rank	Source	Lines
Professor current	Department of Chemistry, Columbia University	2016–	Full	CV	3, 5, 15, 16
Chair, Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 17) chair		2013–2013	Unknown	CV	18, 19
Permanent Member, Synthetic and Biological Chemistry B Study Section, NIH (SBC-B)		2012–2018	Unknown	CV	21
Associate Editor for the Americas, Synlett current		2012–	Unknown	CV	23
Member, Editorial Board, Organic Reactions		2010–2015	Unknown	CV	25
Member, Editorial Board, electronic Encyclopedia of Reagents for Organic Synthesis current		2010–	Unknown	CV	27
John K. Stille Chair	Department of Chemistry, Colorado State University	2008–2016	Distinguished named	CV	29, 30
Professor	Department of Chemistry, Colorado State University	2008–2016	Full	CV	32, 33
Associate Professor	Department of Chemistry, Colorado State University	2005–2008	Associate	CV	35, 36
Assistant Professor	Department of Chemistry, Colorado State University	2000–2005	Assistant	CV	38, 39
NSERC Post-Doctoral Research Fellow	Harvard University	1998–2000	Postdoc	CV	41, 42
Professor			Full	CV current position	3, 15