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Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds

We report here cobalt–N-heterocyclic carbene catalytic systems for the intramolecular decarbonylative coupling through the chelation-assisted C–C bond cleavage of acylindoles and diarylketones. The reaction tolerates a wide range of functional groups such as alkyl, aryl, and heteroaryl groups, givin...

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Detalles Bibliográficos
Autores principales: Yu, Tian-Yang, Xu, Wen-Hua, Lu, Hong, Wei, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162806/
https://www.ncbi.nlm.nih.gov/pubmed/34094442
http://dx.doi.org/10.1039/d0sc04326e
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author Yu, Tian-Yang
Xu, Wen-Hua
Lu, Hong
Wei, Hao
author_facet Yu, Tian-Yang
Xu, Wen-Hua
Lu, Hong
Wei, Hao
author_sort Yu, Tian-Yang
collection PubMed
description We report here cobalt–N-heterocyclic carbene catalytic systems for the intramolecular decarbonylative coupling through the chelation-assisted C–C bond cleavage of acylindoles and diarylketones. The reaction tolerates a wide range of functional groups such as alkyl, aryl, and heteroaryl groups, giving the decarbonylative products in moderate to excellent yields. This transformation involves the cleavage of two C–C bonds and formation of a new C–C bond without the use of noble metals, thus reinforcing the potential application of decarbonylation as an effective tool for C–C bond formation.
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spelling pubmed-81628062021-06-04 Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds Yu, Tian-Yang Xu, Wen-Hua Lu, Hong Wei, Hao Chem Sci Chemistry We report here cobalt–N-heterocyclic carbene catalytic systems for the intramolecular decarbonylative coupling through the chelation-assisted C–C bond cleavage of acylindoles and diarylketones. The reaction tolerates a wide range of functional groups such as alkyl, aryl, and heteroaryl groups, giving the decarbonylative products in moderate to excellent yields. This transformation involves the cleavage of two C–C bonds and formation of a new C–C bond without the use of noble metals, thus reinforcing the potential application of decarbonylation as an effective tool for C–C bond formation. The Royal Society of Chemistry 2020-10-16 /pmc/articles/PMC8162806/ /pubmed/34094442 http://dx.doi.org/10.1039/d0sc04326e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yu, Tian-Yang
Xu, Wen-Hua
Lu, Hong
Wei, Hao
Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title_full Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title_fullStr Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title_full_unstemmed Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title_short Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C–C bonds
title_sort cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of c–c bonds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162806/
https://www.ncbi.nlm.nih.gov/pubmed/34094442
http://dx.doi.org/10.1039/d0sc04326e
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