Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3

A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.

Bibliographic Details
Main Authors:	Xueliang Jiang, Feng-Ling Qing
Format:	Article
Language:	English
Published:	Beilstein-Institut 2013-12-01
Series:	Beilstein Journal of Organic Chemistry
Subjects:	copper methanesulfonates organo-fluorine trifluoromethylation
Online Access:	https://doi.org/10.3762/bjoc.9.322

id	doaj-8adcfce679754aee91d2a79f52f7cdff
record_format	Article
spelling	doaj-8adcfce679754aee91d2a79f52f7cdff2021-02-02T08:25:23ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972013-12-01912862286510.3762/bjoc.9.3221860-5397-9-322Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3Xueliang Jiang0Feng-Ling Qing1Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, ChinaKey Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, ChinaA Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.https://doi.org/10.3762/bjoc.9.322coppermethanesulfonatesorgano-fluorinetrifluoromethylation
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Xueliang Jiang Feng-Ling Qing
spellingShingle	Xueliang Jiang Feng-Ling Qing Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 Beilstein Journal of Organic Chemistry copper methanesulfonates organo-fluorine trifluoromethylation
author_facet	Xueliang Jiang Feng-Ling Qing
author_sort	Xueliang Jiang
title	Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
title_short	Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
title_full	Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
title_fullStr	Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
title_full_unstemmed	Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
title_sort	cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with tmscf3
publisher	Beilstein-Institut
series	Beilstein Journal of Organic Chemistry
issn	1860-5397
publishDate	2013-12-01
description	A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.
topic	copper methanesulfonates organo-fluorine trifluoromethylation
url	https://doi.org/10.3762/bjoc.9.322
work_keys_str_mv	AT xueliangjiang cumediatedtrifluoromethylationofbenzylallylandpropargylmethanesulfonateswithtmscf3 AT fenglingqing cumediatedtrifluoromethylationofbenzylallylandpropargylmethanesulfonateswithtmscf3
_version_	1724297159652671488

Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3

Similar Items