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Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent
The direct C–H trifluoromethylation of alkynes and quinoxalinones has been achieved using a graphene oxide/Langlois' reagent system. This multi-component tandem reaction using graphene oxide as the catalyst and Langlois' reagent as the robust CF(3) radical source results in the formation o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044184/ https://www.ncbi.nlm.nih.gov/pubmed/35493205 http://dx.doi.org/10.1039/d1ra07014b |
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author | Li, Hong Peng, Xiangjun Nie, Liang Zhou, Lin Yang, Ming Li, Fan Hu, Jian Yao, Zhiyang Liu, Liangxian |
author_facet | Li, Hong Peng, Xiangjun Nie, Liang Zhou, Lin Yang, Ming Li, Fan Hu, Jian Yao, Zhiyang Liu, Liangxian |
author_sort | Li, Hong |
collection | PubMed |
description | The direct C–H trifluoromethylation of alkynes and quinoxalinones has been achieved using a graphene oxide/Langlois' reagent system. This multi-component tandem reaction using graphene oxide as the catalyst and Langlois' reagent as the robust CF(3) radical source results in the formation of olefinic C–CF(3) to access a series of 3-trifluoroalkylated quinoxalin-2(1H)-ones. |
format | Online Article Text |
id | pubmed-9044184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90441842022-04-28 Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent Li, Hong Peng, Xiangjun Nie, Liang Zhou, Lin Yang, Ming Li, Fan Hu, Jian Yao, Zhiyang Liu, Liangxian RSC Adv Chemistry The direct C–H trifluoromethylation of alkynes and quinoxalinones has been achieved using a graphene oxide/Langlois' reagent system. This multi-component tandem reaction using graphene oxide as the catalyst and Langlois' reagent as the robust CF(3) radical source results in the formation of olefinic C–CF(3) to access a series of 3-trifluoroalkylated quinoxalin-2(1H)-ones. The Royal Society of Chemistry 2021-12-01 /pmc/articles/PMC9044184/ /pubmed/35493205 http://dx.doi.org/10.1039/d1ra07014b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Li, Hong Peng, Xiangjun Nie, Liang Zhou, Lin Yang, Ming Li, Fan Hu, Jian Yao, Zhiyang Liu, Liangxian Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title | Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title_full | Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title_fullStr | Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title_full_unstemmed | Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title_short | Graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and Langlois' reagent |
title_sort | graphene oxide-catalyzed trifluoromethylation of alkynes with quinoxalinones and langlois' reagent |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044184/ https://www.ncbi.nlm.nih.gov/pubmed/35493205 http://dx.doi.org/10.1039/d1ra07014b |
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