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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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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. |
format | Online Article Text |
id | pubmed-9977451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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