Issue 47, 2014

Silver-mediated oxidative vinylic C–H bond sulfenylation of enamides with disulfides

Abstract

A silver-mediated oxidative vinylic C–H bond sulfenylation of enamides was developed. This method is compatible with diaryl and dialkyl disulfides to deliver biologically precious chalcogenated olefins efficiently. A plausible non-chain radical mechanism was proposed for understanding this novel sulfenylation based on the mechanistic studies.

Graphical abstract: Silver-mediated oxidative vinylic C–H bond sulfenylation of enamides with disulfides

Supplementary files

Article information

Article type
Communication
Submitted
16 Sep 2014
Accepted
15 Oct 2014
First published
15 Oct 2014

Org. Biomol. Chem., 2014,12, 9519-9523

Author version available

Silver-mediated oxidative vinylic C–H bond sulfenylation of enamides with disulfides

L. Yang, Q. Wen, F. Xiao and G. Deng, Org. Biomol. Chem., 2014, 12, 9519 DOI: 10.1039/C4OB01970A

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