Issue 8, 2015

Byproduct promoted regioselective sulfenylation of indoles with sulfinic acids

Abstract

An unprecedented method to synthesise 3-sulfenylindoles is demonstrated via byproduct promoted sulfenylation of indoles with sulfinic acids in the absence of an external catalyst. The reaction selectively afforded structurally diverse indole thioethers in good to excellent yields in 1,2-dichloroethane at 80 °C.

Graphical abstract: Byproduct promoted regioselective sulfenylation of indoles with sulfinic acids

Supplementary files

Article information

Article type
Communication
Submitted
10 Dec 2014
Accepted
05 Jan 2015
First published
05 Jan 2015

Org. Biomol. Chem., 2015,13, 2251-2254

Byproduct promoted regioselective sulfenylation of indoles with sulfinic acids

C. Liu and L. Ding, Org. Biomol. Chem., 2015, 13, 2251 DOI: 10.1039/C4OB02575J

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