Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783626212238688256 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7754511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yefei arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT bergerflorian arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT jiahao arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT fordjoseph arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT wortmanalan arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT borgeljonas arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT genicotchristophe arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation AT rittertobias arylsulfoniumsaltsforsiteselectivelatestagetrifluoromethylation |