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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7756274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
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title_fullStr | Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
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title_full_unstemmed | Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
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title_short | Direct β‐ and γ‐C(sp(3))−H Alkynylation of Free Carboxylic Acids
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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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