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Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involv...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537669/ https://www.ncbi.nlm.nih.gov/pubmed/37764480 http://dx.doi.org/10.3390/molecules28186704 |
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author | Maret, Corentin David, Nicolas Pierrot, David Léonel, Eric Levacher, Vincent Brière, Jean-François Oudeyer, Sylvain |
author_facet | Maret, Corentin David, Nicolas Pierrot, David Léonel, Eric Levacher, Vincent Brière, Jean-François Oudeyer, Sylvain |
author_sort | Maret, Corentin |
collection | PubMed |
description | The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involved in several chemical transformations, underlining their potential as versatile intermediates in synthetic chemistry. A mechanism was also proposed based upon a control experiment and cyclic voltammetry (CV) study. |
format | Online Article Text |
id | pubmed-10537669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105376692023-09-29 Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives Maret, Corentin David, Nicolas Pierrot, David Léonel, Eric Levacher, Vincent Brière, Jean-François Oudeyer, Sylvain Molecules Article The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involved in several chemical transformations, underlining their potential as versatile intermediates in synthetic chemistry. A mechanism was also proposed based upon a control experiment and cyclic voltammetry (CV) study. MDPI 2023-09-20 /pmc/articles/PMC10537669/ /pubmed/37764480 http://dx.doi.org/10.3390/molecules28186704 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Maret, Corentin David, Nicolas Pierrot, David Léonel, Eric Levacher, Vincent Brière, Jean-François Oudeyer, Sylvain Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title | Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title_full | Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title_fullStr | Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title_full_unstemmed | Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title_short | Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives |
title_sort | synthesis of α-chloroarylacetic acid via electrochemical carboxylation of α,α-dichloroarylmethane derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537669/ https://www.ncbi.nlm.nih.gov/pubmed/37764480 http://dx.doi.org/10.3390/molecules28186704 |
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