Issue 8, 2018

Copper-catalyzed carbene insertion into the sulfur–sulfur bond of benzenesulfonothioate

Abstract

An unprecedented copper-catalyzed intermolecular sulfur–sulfur bond insertion between aryldiazoacetates and benzenesulfonothioate has been successfully developed. Diverse α-disulfur functionalized esters were synthesized in good to excellent yields. The sulfur ylide formation and subsequent Stevens rearrangement are considered as the key steps for the discovered reaction.

Graphical abstract: Copper-catalyzed carbene insertion into the sulfur–sulfur bond of benzenesulfonothioate

Supplementary files

Article information

Article type
Research Article
Submitted
18 Dec 2017
Accepted
23 Feb 2018
First published
24 Feb 2018

Org. Chem. Front., 2018,5, 1371-1374

Copper-catalyzed carbene insertion into the sulfur–sulfur bond of benzenesulfonothioate

H. Yuan, T. Nuligonda, H. Gao, C. Tung and Z. Xu, Org. Chem. Front., 2018, 5, 1371 DOI: 10.1039/C7QO01131H

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