Issue 15, 2019

Metal free, facile sulfenylation of ketene dithioacetals catalyzed by an HBr–DMSO system

Abstract

A transition metal free, highly efficient, sulfenylation of ketene dithioacetals catalyzed by an HBr–DMSO system is achieved. This strategy employs inexpensive and readily available HBr and DMSO to provide a direct C–H bond sulfenylation with a broad range of aryl thiols. Highlights of the present strategy are convenient, straightforward approach, metal free, short reaction time and excellent yields. This sulfenylated product is also successfully transformed for the synthesis of pyrazole derivatives in excellent yields.

Graphical abstract: Metal free, facile sulfenylation of ketene dithioacetals catalyzed by an HBr–DMSO system

Supplementary files

Article information

Article type
Paper
Submitted
21 Feb 2019
Accepted
12 Mar 2019
First published
27 Mar 2019

New J. Chem., 2019,43, 5996-6000

Metal free, facile sulfenylation of ketene dithioacetals catalyzed by an HBr–DMSO system

G. S. Sorabad and M. R. Maddani, New J. Chem., 2019, 43, 5996 DOI: 10.1039/C9NJ00925F

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