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C−H Carboxylation of Aromatic Compounds through CO(2) Fixation

Carbon dioxide (CO(2)) represents the most abundant and accessible carbon source on Earth. Thus the ability to transform CO(2) into valuable commodity chemicals through the construction of C−C bonds is an invaluable strategy. Carboxylic acids and derivatives, the main products obtained by carboxylat...

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Detalles Bibliográficos
Autores principales: Luo, Junfei, Larrosa, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601192/
https://www.ncbi.nlm.nih.gov/pubmed/28722818
http://dx.doi.org/10.1002/cssc.201701058
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author Luo, Junfei
Larrosa, Igor
author_facet Luo, Junfei
Larrosa, Igor
author_sort Luo, Junfei
collection PubMed
description Carbon dioxide (CO(2)) represents the most abundant and accessible carbon source on Earth. Thus the ability to transform CO(2) into valuable commodity chemicals through the construction of C−C bonds is an invaluable strategy. Carboxylic acids and derivatives, the main products obtained by carboxylation of carbon nucleophiles by reaction of CO(2), have wide application in pharmaceuticals and advanced materials. Among the variety of carboxylation methods currently available, the direct carboxylation of C−H bonds with CO(2) has attracted much attention owing to advantages from a step‐ and atom‐economical point of view. In particular, the prevalence of (hetero)aromatic carboxylic acids and derivatives among biologically active compounds has led to significant interest in the development of methods for their direct carboxylation from CO(2). Herein, the latest achievements in the area of direct C−H carboxylation of (hetero)aromatic compounds with CO(2) will be discussed.
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spelling pubmed-56011922017-10-03 C−H Carboxylation of Aromatic Compounds through CO(2) Fixation Luo, Junfei Larrosa, Igor ChemSusChem Minireviews Carbon dioxide (CO(2)) represents the most abundant and accessible carbon source on Earth. Thus the ability to transform CO(2) into valuable commodity chemicals through the construction of C−C bonds is an invaluable strategy. Carboxylic acids and derivatives, the main products obtained by carboxylation of carbon nucleophiles by reaction of CO(2), have wide application in pharmaceuticals and advanced materials. Among the variety of carboxylation methods currently available, the direct carboxylation of C−H bonds with CO(2) has attracted much attention owing to advantages from a step‐ and atom‐economical point of view. In particular, the prevalence of (hetero)aromatic carboxylic acids and derivatives among biologically active compounds has led to significant interest in the development of methods for their direct carboxylation from CO(2). Herein, the latest achievements in the area of direct C−H carboxylation of (hetero)aromatic compounds with CO(2) will be discussed. John Wiley and Sons Inc. 2017-08-16 2017-09-11 /pmc/articles/PMC5601192/ /pubmed/28722818 http://dx.doi.org/10.1002/cssc.201701058 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (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 Minireviews
Luo, Junfei
Larrosa, Igor
C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title_full C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title_fullStr C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title_full_unstemmed C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title_short C−H Carboxylation of Aromatic Compounds through CO(2) Fixation
title_sort c−h carboxylation of aromatic compounds through co(2) fixation
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601192/
https://www.ncbi.nlm.nih.gov/pubmed/28722818
http://dx.doi.org/10.1002/cssc.201701058
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