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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...

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Autores principales: Gevorgyan, Ashot, Hopmann, Kathrin H., Bayer, Annette
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
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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.
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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
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