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Pd-catalysed C–H functionalisation of free carboxylic acids

Pd-catalysed C–H functionalisation of free carboxylic acids has drawn significant attention over the last few years due to the predominance of carboxylic acid moieties in pharmaceuticals and agrochemicals. But their coordinating ability was overlooked and masked by exogenous directing groups for a l...

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Autores principales: Dutta, Suparna, Bhattacharya, Trisha, Geffers, Finn J., Bürger, Marcel, Maiti, Debabrata, Werz, Daniel B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890104/
https://www.ncbi.nlm.nih.gov/pubmed/35340865
http://dx.doi.org/10.1039/d1sc05392b
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author Dutta, Suparna
Bhattacharya, Trisha
Geffers, Finn J.
Bürger, Marcel
Maiti, Debabrata
Werz, Daniel B.
author_facet Dutta, Suparna
Bhattacharya, Trisha
Geffers, Finn J.
Bürger, Marcel
Maiti, Debabrata
Werz, Daniel B.
author_sort Dutta, Suparna
collection PubMed
description Pd-catalysed C–H functionalisation of free carboxylic acids has drawn significant attention over the last few years due to the predominance of carboxylic acid moieties in pharmaceuticals and agrochemicals. But their coordinating ability was overlooked and masked by exogenous directing groups for a long time. Even other crucial roles of carboxylic acids as additives and steric inducers that directly influence the mode of a reaction have been widely neglected. This review aims to embrace all of the diverse aspects of carboxylic acids except additive and steric effects by concisely and systematically describing their versatile role in Pd-catalysed proximal and distal C–H activation reactions that could be implemented in the pharmaceutical and agrochemical industries. In addition, the mechanistic perspectives along with several recent strategies developed in the last few years discussed here will serve as educational resources for future research.
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spelling pubmed-88901042022-03-24 Pd-catalysed C–H functionalisation of free carboxylic acids Dutta, Suparna Bhattacharya, Trisha Geffers, Finn J. Bürger, Marcel Maiti, Debabrata Werz, Daniel B. Chem Sci Chemistry Pd-catalysed C–H functionalisation of free carboxylic acids has drawn significant attention over the last few years due to the predominance of carboxylic acid moieties in pharmaceuticals and agrochemicals. But their coordinating ability was overlooked and masked by exogenous directing groups for a long time. Even other crucial roles of carboxylic acids as additives and steric inducers that directly influence the mode of a reaction have been widely neglected. This review aims to embrace all of the diverse aspects of carboxylic acids except additive and steric effects by concisely and systematically describing their versatile role in Pd-catalysed proximal and distal C–H activation reactions that could be implemented in the pharmaceutical and agrochemical industries. In addition, the mechanistic perspectives along with several recent strategies developed in the last few years discussed here will serve as educational resources for future research. The Royal Society of Chemistry 2022-01-10 /pmc/articles/PMC8890104/ /pubmed/35340865 http://dx.doi.org/10.1039/d1sc05392b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Dutta, Suparna
Bhattacharya, Trisha
Geffers, Finn J.
Bürger, Marcel
Maiti, Debabrata
Werz, Daniel B.
Pd-catalysed C–H functionalisation of free carboxylic acids
title Pd-catalysed C–H functionalisation of free carboxylic acids
title_full Pd-catalysed C–H functionalisation of free carboxylic acids
title_fullStr Pd-catalysed C–H functionalisation of free carboxylic acids
title_full_unstemmed Pd-catalysed C–H functionalisation of free carboxylic acids
title_short Pd-catalysed C–H functionalisation of free carboxylic acids
title_sort pd-catalysed c–h functionalisation of free carboxylic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890104/
https://www.ncbi.nlm.nih.gov/pubmed/35340865
http://dx.doi.org/10.1039/d1sc05392b
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