Cargando…
Formal C−H Carboxylation of Unactivated Arenes
A formal C−H carboxylation of unactivated arenes using CO(2) in green solvents is described. The present strategy combines a sterically controlled Ir‐catalyzed C−H borylation followed by a Cu‐catalyzed carboxylation of the in situ generated organoboronates. The reaction is highly regioselective for...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317471/ https://www.ncbi.nlm.nih.gov/pubmed/32003869 http://dx.doi.org/10.1002/chem.202000515 |
_version_ | 1783550635706155008 |
---|---|
author | Gevorgyan, Ashot Hopmann, Kathrin H. Bayer, Annette |
author_facet | Gevorgyan, Ashot Hopmann, Kathrin H. Bayer, Annette |
author_sort | Gevorgyan, Ashot |
collection | PubMed |
description | A formal C−H carboxylation of unactivated arenes using CO(2) in green solvents is described. The present strategy combines a sterically controlled Ir‐catalyzed C−H borylation followed by a Cu‐catalyzed carboxylation of the in situ generated organoboronates. The reaction is highly regioselective for the C−H carboxylation of 1,3‐disubstituted and 1,2,3‐trisubstituted benzenes, 1,2‐ or 1,4‐symmetrically substituted benzenes, fluorinated benzenes and different heterocycles. The developed methodology was applied to the late‐stage C−H carboxylation of commercial drugs and ligands. |
format | Online Article Text |
id | pubmed-7317471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73174712020-06-30 Formal C−H Carboxylation of Unactivated Arenes Gevorgyan, Ashot Hopmann, Kathrin H. Bayer, Annette Chemistry Full Papers A formal C−H carboxylation of unactivated arenes using CO(2) in green solvents is described. The present strategy combines a sterically controlled Ir‐catalyzed C−H borylation followed by a Cu‐catalyzed carboxylation of the in situ generated organoboronates. The reaction is highly regioselective for the C−H carboxylation of 1,3‐disubstituted and 1,2,3‐trisubstituted benzenes, 1,2‐ or 1,4‐symmetrically substituted benzenes, fluorinated benzenes and different heterocycles. The developed methodology was applied to the late‐stage C−H carboxylation of commercial drugs and ligands. John Wiley and Sons Inc. 2020-05-04 2020-05-12 /pmc/articles/PMC7317471/ /pubmed/32003869 http://dx.doi.org/10.1002/chem.202000515 Text en © 2020 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 | Full Papers Gevorgyan, Ashot Hopmann, Kathrin H. Bayer, Annette Formal C−H Carboxylation of Unactivated Arenes |
title | Formal C−H Carboxylation of Unactivated Arenes |
title_full | Formal C−H Carboxylation of Unactivated Arenes |
title_fullStr | Formal C−H Carboxylation of Unactivated Arenes |
title_full_unstemmed | Formal C−H Carboxylation of Unactivated Arenes |
title_short | Formal C−H Carboxylation of Unactivated Arenes |
title_sort | formal c−h carboxylation of unactivated arenes |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317471/ https://www.ncbi.nlm.nih.gov/pubmed/32003869 http://dx.doi.org/10.1002/chem.202000515 |
work_keys_str_mv | AT gevorgyanashot formalchcarboxylationofunactivatedarenes AT hopmannkathrinh formalchcarboxylationofunactivatedarenes AT bayerannette formalchcarboxylationofunactivatedarenes |