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1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids
1,1-Difluoroethylated aromatics are of great importance in medicinal chemistry and related fields. 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a cheap and abundant industrial raw material, is viewed as an ideal 1,1-difluoroethylating reagent, but the direct introduction of the difluoroethyl (CF(2)CH(...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071211/ https://www.ncbi.nlm.nih.gov/pubmed/35529618 http://dx.doi.org/10.1039/c9ra06406k |
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author | Liu, Jianchang Zhang, Jida Wu, Chaolin Liu, Hefu Liu, Hui Sun, Fenggang Li, Yueyun Liu, Yuying Dong, Yunhui Li, Xinjin |
author_facet | Liu, Jianchang Zhang, Jida Wu, Chaolin Liu, Hefu Liu, Hui Sun, Fenggang Li, Yueyun Liu, Yuying Dong, Yunhui Li, Xinjin |
author_sort | Liu, Jianchang |
collection | PubMed |
description | 1,1-Difluoroethylated aromatics are of great importance in medicinal chemistry and related fields. 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a cheap and abundant industrial raw material, is viewed as an ideal 1,1-difluoroethylating reagent, but the direct introduction of the difluoroethyl (CF(2)CH(3)) group onto aromatic rings using CH(3)CF(2)Cl has not been successfully accomplished. Herein, we disclose a nickel-catalyzed 1,1-difluoroethylation of arylboronic acids with CH(3)CF(2)Cl for the synthesis of (1,1-difluoroethyl)arenes. |
format | Online Article Text |
id | pubmed-9071211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90712112022-05-06 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids Liu, Jianchang Zhang, Jida Wu, Chaolin Liu, Hefu Liu, Hui Sun, Fenggang Li, Yueyun Liu, Yuying Dong, Yunhui Li, Xinjin RSC Adv Chemistry 1,1-Difluoroethylated aromatics are of great importance in medicinal chemistry and related fields. 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a cheap and abundant industrial raw material, is viewed as an ideal 1,1-difluoroethylating reagent, but the direct introduction of the difluoroethyl (CF(2)CH(3)) group onto aromatic rings using CH(3)CF(2)Cl has not been successfully accomplished. Herein, we disclose a nickel-catalyzed 1,1-difluoroethylation of arylboronic acids with CH(3)CF(2)Cl for the synthesis of (1,1-difluoroethyl)arenes. The Royal Society of Chemistry 2019-09-09 /pmc/articles/PMC9071211/ /pubmed/35529618 http://dx.doi.org/10.1039/c9ra06406k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Liu, Jianchang Zhang, Jida Wu, Chaolin Liu, Hefu Liu, Hui Sun, Fenggang Li, Yueyun Liu, Yuying Dong, Yunhui Li, Xinjin 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title | 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title_full | 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title_fullStr | 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title_full_unstemmed | 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title_short | 1,1-Difluoroethyl chloride (CH(3)CF(2)Cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
title_sort | 1,1-difluoroethyl chloride (ch(3)cf(2)cl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071211/ https://www.ncbi.nlm.nih.gov/pubmed/35529618 http://dx.doi.org/10.1039/c9ra06406k |
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