Issue 11, 2017

Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates

Abstract

A nucleophilic trifluorovinylation of organothiocyanates catalyzed by tetrabutylammonium fluoride has been developed. In this transformation, a variety of aryl and alkyl thiocyanates reacted with trifluorovinyl trimethylsilane to afford 1,2,2-trifluorovinyl sulphides. This transformation was extended to organic selenocyanates to afford 1,2,2-trifluorovinyl selenides. The presented methodology is simple and mild, and can also be used to prepare 1,2,2-trifluorovinyl sulphoxides from organothiocyanates.

Graphical abstract: Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates

Supplementary files

Article information

Article type
Research Article
Submitted
17 Jul 2017
Accepted
16 Aug 2017
First published
16 Aug 2017

Org. Chem. Front., 2017,4, 2226-2229

Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates

Y. Zhang, D. Wu and Z. Weng, Org. Chem. Front., 2017, 4, 2226 DOI: 10.1039/C7QO00595D

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