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Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates

We report a three-component olefin reductive dicarbofunctionalization for constructing alkylborates, specifically, nickel-catalyzed reductive dialkylation and alkylarylation of vinyl boronates with a variety of alkyl bromides and aryl iodides. This reaction exhibits good coupling efficiency and exce...

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Detalles Bibliográficos
Autores principales: Wang, Xiao-Xu, Lu, Xi, He, Shi-Jiang, Fu, Yao
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/PMC8163243/
https://www.ncbi.nlm.nih.gov/pubmed/34094163
http://dx.doi.org/10.1039/d0sc02054k
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author Wang, Xiao-Xu
Lu, Xi
He, Shi-Jiang
Fu, Yao
author_facet Wang, Xiao-Xu
Lu, Xi
He, Shi-Jiang
Fu, Yao
author_sort Wang, Xiao-Xu
collection PubMed
description We report a three-component olefin reductive dicarbofunctionalization for constructing alkylborates, specifically, nickel-catalyzed reductive dialkylation and alkylarylation of vinyl boronates with a variety of alkyl bromides and aryl iodides. This reaction exhibits good coupling efficiency and excellent functional group compatibility, providing convenient access to the late-stage modification of complex natural products and drug molecules. Combined with alkylborate transformations, this reaction could also find applications in the modular and convergent synthesis of complex compounds.
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spelling pubmed-81632432021-06-04 Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates Wang, Xiao-Xu Lu, Xi He, Shi-Jiang Fu, Yao Chem Sci Chemistry We report a three-component olefin reductive dicarbofunctionalization for constructing alkylborates, specifically, nickel-catalyzed reductive dialkylation and alkylarylation of vinyl boronates with a variety of alkyl bromides and aryl iodides. This reaction exhibits good coupling efficiency and excellent functional group compatibility, providing convenient access to the late-stage modification of complex natural products and drug molecules. Combined with alkylborate transformations, this reaction could also find applications in the modular and convergent synthesis of complex compounds. The Royal Society of Chemistry 2020-07-08 /pmc/articles/PMC8163243/ /pubmed/34094163 http://dx.doi.org/10.1039/d0sc02054k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Xiao-Xu
Lu, Xi
He, Shi-Jiang
Fu, Yao
Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title_full Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title_fullStr Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title_full_unstemmed Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title_short Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
title_sort nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163243/
https://www.ncbi.nlm.nih.gov/pubmed/34094163
http://dx.doi.org/10.1039/d0sc02054k
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