Issue 6, 2017

Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway

Abstract

A novel and convenient method has been developed for the 1,2-selenosulfonylation of alkynes under metal-free conditions. The reaction avoids the need for the pre-prepared Se–S reagents, providing facile access to a series of β-(seleno)vinyl sulfones with high levels of regio- and stereoselectivity. The key features of this reaction include broad substrate scope, excellent functional-group tolerance, readily available reagents and amenability to gram-scale synthesis. Preliminary mechanistic studies support the proposed cationic-species-induced pathway.

Graphical abstract: Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway

Supplementary files

Article information

Article type
Communication
Submitted
12 Dec 2016
Accepted
20 Jan 2017
First published
20 Jan 2017

Green Chem., 2017,19, 1490-1493

Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway

K. Sun, X. Wang, F. Fu, C. Zhang, Y. Chen and L. Liu, Green Chem., 2017, 19, 1490 DOI: 10.1039/C6GC03420A

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