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Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins

Herein, we report unprecedented aluminum-catalyzed halodefluorination reactions of trifluoromethyl- and difluoroalkyl-substituted olefins with bromo- or chlorotrimethylsilane. The interesting feature of these reactions is that one, two, or three fluorine atoms can be selectively replaced with bromin...

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Autores principales: Liu, Zhong, Tu, Xian-Shuang, Guo, Le-Tao, Wang, Xiao-Chen
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/PMC8162833/
https://www.ncbi.nlm.nih.gov/pubmed/34094400
http://dx.doi.org/10.1039/d0sc03883k
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author Liu, Zhong
Tu, Xian-Shuang
Guo, Le-Tao
Wang, Xiao-Chen
author_facet Liu, Zhong
Tu, Xian-Shuang
Guo, Le-Tao
Wang, Xiao-Chen
author_sort Liu, Zhong
collection PubMed
description Herein, we report unprecedented aluminum-catalyzed halodefluorination reactions of trifluoromethyl- and difluoroalkyl-substituted olefins with bromo- or chlorotrimethylsilane. The interesting feature of these reactions is that one, two, or three fluorine atoms can be selectively replaced with bromine or chlorine atoms by modification of the reaction conditions. The generated products can undergo a variety of subsequent transformations, thus constituting a valuable stock of building blocks for installing fluorine-containing olefin motifs in other molecules.
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spelling pubmed-81628332021-06-04 Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins Liu, Zhong Tu, Xian-Shuang Guo, Le-Tao Wang, Xiao-Chen Chem Sci Chemistry Herein, we report unprecedented aluminum-catalyzed halodefluorination reactions of trifluoromethyl- and difluoroalkyl-substituted olefins with bromo- or chlorotrimethylsilane. The interesting feature of these reactions is that one, two, or three fluorine atoms can be selectively replaced with bromine or chlorine atoms by modification of the reaction conditions. The generated products can undergo a variety of subsequent transformations, thus constituting a valuable stock of building blocks for installing fluorine-containing olefin motifs in other molecules. The Royal Society of Chemistry 2020-10-01 /pmc/articles/PMC8162833/ /pubmed/34094400 http://dx.doi.org/10.1039/d0sc03883k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Liu, Zhong
Tu, Xian-Shuang
Guo, Le-Tao
Wang, Xiao-Chen
Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title_full Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title_fullStr Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title_full_unstemmed Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title_short Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
title_sort aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162833/
https://www.ncbi.nlm.nih.gov/pubmed/34094400
http://dx.doi.org/10.1039/d0sc03883k
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