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Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation

Incorporation of the CF(3) group into arenes has found increasing importance in drug discovery. Herein, we report the first photoredox‐catalyzed cross‐coupling of aryl thianthrenium salts with a copper‐based trifluoromethyl reagent, which enables a site‐selective late‐stage trifluoromethylation of a...

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Autores principales: Ye, Fei, Berger, Florian, Jia, Hao, Ford, Joseph, Wortman, Alan, Börgel, Jonas, Genicot, Christophe, Ritter, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754511/
https://www.ncbi.nlm.nih.gov/pubmed/31389649
http://dx.doi.org/10.1002/anie.201906672
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author Ye, Fei
Berger, Florian
Jia, Hao
Ford, Joseph
Wortman, Alan
Börgel, Jonas
Genicot, Christophe
Ritter, Tobias
author_facet Ye, Fei
Berger, Florian
Jia, Hao
Ford, Joseph
Wortman, Alan
Börgel, Jonas
Genicot, Christophe
Ritter, Tobias
author_sort Ye, Fei
collection PubMed
description Incorporation of the CF(3) group into arenes has found increasing importance in drug discovery. Herein, we report the first photoredox‐catalyzed cross‐coupling of aryl thianthrenium salts with a copper‐based trifluoromethyl reagent, which enables a site‐selective late‐stage trifluoromethylation of arenes. The reaction proceeds with broad functional group tolerance, even for complex small molecules on gram scale. The method was further extended to produce pentafluoroethylated derivatives.
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spelling pubmed-77545112020-12-28 Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation Ye, Fei Berger, Florian Jia, Hao Ford, Joseph Wortman, Alan Börgel, Jonas Genicot, Christophe Ritter, Tobias Angew Chem Int Ed Engl Communications Incorporation of the CF(3) group into arenes has found increasing importance in drug discovery. Herein, we report the first photoredox‐catalyzed cross‐coupling of aryl thianthrenium salts with a copper‐based trifluoromethyl reagent, which enables a site‐selective late‐stage trifluoromethylation of arenes. The reaction proceeds with broad functional group tolerance, even for complex small molecules on gram scale. The method was further extended to produce pentafluoroethylated derivatives. John Wiley and Sons Inc. 2019-09-04 2019-10-07 /pmc/articles/PMC7754511/ /pubmed/31389649 http://dx.doi.org/10.1002/anie.201906672 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Ye, Fei
Berger, Florian
Jia, Hao
Ford, Joseph
Wortman, Alan
Börgel, Jonas
Genicot, Christophe
Ritter, Tobias
Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title_full Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title_fullStr Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title_full_unstemmed Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title_short Aryl Sulfonium Salts for Site‐Selective Late‐Stage Trifluoromethylation
title_sort aryl sulfonium salts for site‐selective late‐stage trifluoromethylation
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754511/
https://www.ncbi.nlm.nih.gov/pubmed/31389649
http://dx.doi.org/10.1002/anie.201906672
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