Issue 62, 2014

Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

Abstract

A new method for the preparation of alkyl aryl sulfides through direct oxidative thiolation of alkanes or ethers with arylsulfonyl hydrazides using di-tert-butyl peroxide (DTBP) as an oxidant catalyzed by Pd(OAc)2 has been reported. The C–H bonds in various alkanes or ethers were successfully converted into C–S bonds to yield the corresponding sulfides in moderate to good yields.

Graphical abstract: Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

Supplementary files

Article information

Article type
Communication
Submitted
25 Apr 2014
Accepted
07 Jun 2014
First published
12 Jun 2014

Chem. Commun., 2014,50, 8578-8581

Author version available

Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

S. Guo, W. He, J. Xiang and Y. Yuan, Chem. Commun., 2014, 50, 8578 DOI: 10.1039/C4CC02876G

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