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Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes

An unprecedented but challenging defluorinative arylboration has been achieved. Enabled by a copper catalyst, an interesting procedure on defluorinative arylboration of styrenes has been established. With polyfluoroarenes as the substrates, this methodology offers flexible and facile access to provi...

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Autores principales: Wu, Fu-Peng, Gu, Xing-Wei, Geng, Hui-Qing, Wu, Xiao-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977451/
https://www.ncbi.nlm.nih.gov/pubmed/36873842
http://dx.doi.org/10.1039/d2sc06472c
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author Wu, Fu-Peng
Gu, Xing-Wei
Geng, Hui-Qing
Wu, Xiao-Feng
author_facet Wu, Fu-Peng
Gu, Xing-Wei
Geng, Hui-Qing
Wu, Xiao-Feng
author_sort Wu, Fu-Peng
collection PubMed
description An unprecedented but challenging defluorinative arylboration has been achieved. Enabled by a copper catalyst, an interesting procedure on defluorinative arylboration of styrenes has been established. With polyfluoroarenes as the substrates, this methodology offers flexible and facile access to provide a diverse assortment of products under mild reaction conditions. In addition, by using a chiral phosphine ligand, an enantioselective defluorinative arylboration was also realized, affording a set of chiral products with unprecedented levels of enantioselectivity.
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spelling pubmed-99774512023-03-02 Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes Wu, Fu-Peng Gu, Xing-Wei Geng, Hui-Qing Wu, Xiao-Feng Chem Sci Chemistry An unprecedented but challenging defluorinative arylboration has been achieved. Enabled by a copper catalyst, an interesting procedure on defluorinative arylboration of styrenes has been established. With polyfluoroarenes as the substrates, this methodology offers flexible and facile access to provide a diverse assortment of products under mild reaction conditions. In addition, by using a chiral phosphine ligand, an enantioselective defluorinative arylboration was also realized, affording a set of chiral products with unprecedented levels of enantioselectivity. The Royal Society of Chemistry 2023-02-06 /pmc/articles/PMC9977451/ /pubmed/36873842 http://dx.doi.org/10.1039/d2sc06472c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Wu, Fu-Peng
Gu, Xing-Wei
Geng, Hui-Qing
Wu, Xiao-Feng
Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title_full Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title_fullStr Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title_full_unstemmed Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title_short Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
title_sort copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977451/
https://www.ncbi.nlm.nih.gov/pubmed/36873842
http://dx.doi.org/10.1039/d2sc06472c
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