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Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids

In this study we report the identification of a novel class of ligands for palladium‐catalyzed C(sp(3))−H activation that enables the direct alkynylation of free carboxylic acid substrates. In contrast to previous synthetic methods, no introduction/removal of an exogenous directing group is required...

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Detalles Bibliográficos
Autores principales: Ghiringhelli, Francesca, Uttry, Alexander, Ghosh, Kiron Kumar, van Gemmeren, Manuel
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/PMC7756274/
https://www.ncbi.nlm.nih.gov/pubmed/32898310
http://dx.doi.org/10.1002/anie.202010784
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author Ghiringhelli, Francesca
Uttry, Alexander
Ghosh, Kiron Kumar
van Gemmeren, Manuel
author_facet Ghiringhelli, Francesca
Uttry, Alexander
Ghosh, Kiron Kumar
van Gemmeren, Manuel
author_sort Ghiringhelli, Francesca
collection PubMed
description In this study we report the identification of a novel class of ligands for palladium‐catalyzed C(sp(3))−H activation that enables the direct alkynylation of free carboxylic acid substrates. In contrast to previous synthetic methods, no introduction/removal of an exogenous directing group is required. A broad scope of acids including both α‐quaternary and challenging α‐non‐quaternary can be used as substrates. Additionally, the alkynylation in the distal γ‐position is reported. Finally, this study encompasses preliminary findings on an enantioselective variant of the title transformation as well as synthetic applications of the products obtained.
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spelling pubmed-77562742020-12-28 Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids Ghiringhelli, Francesca Uttry, Alexander Ghosh, Kiron Kumar van Gemmeren, Manuel Angew Chem Int Ed Engl Communications In this study we report the identification of a novel class of ligands for palladium‐catalyzed C(sp(3))−H activation that enables the direct alkynylation of free carboxylic acid substrates. In contrast to previous synthetic methods, no introduction/removal of an exogenous directing group is required. A broad scope of acids including both α‐quaternary and challenging α‐non‐quaternary can be used as substrates. Additionally, the alkynylation in the distal γ‐position is reported. Finally, this study encompasses preliminary findings on an enantioselective variant of the title transformation as well as synthetic applications of the products obtained. John Wiley and Sons Inc. 2020-10-12 2020-12-14 /pmc/articles/PMC7756274/ /pubmed/32898310 http://dx.doi.org/10.1002/anie.202010784 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Ghiringhelli, Francesca
Uttry, Alexander
Ghosh, Kiron Kumar
van Gemmeren, Manuel
Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title_full Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title_fullStr Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title_full_unstemmed Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title_short Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
title_sort direct β‐ and γ‐c(sp(3))−h alkynylation of free carboxylic acids
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756274/
https://www.ncbi.nlm.nih.gov/pubmed/32898310
http://dx.doi.org/10.1002/anie.202010784
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