Issue 1, 2019

Transition metal-free base-promoted arylation of sulfenate anions with diaryliodonium salts

Abstract

A transition metal-free, base-promoted arylation of general sulfenate anions with diaryliodonium salts as an aryl source was developed under mild conditions. Retro-Michael reaction and C–S bond formation were involved in this transformation leading to diaryl and aryl alkyl sulfoxides in good yields. This procedure has general substrate scope and is easy to scale-up.

Graphical abstract: Transition metal-free base-promoted arylation of sulfenate anions with diaryliodonium salts

Supplementary files

Article information

Article type
Research Article
Submitted
23 Aug 2018
Accepted
31 Oct 2018
First published
01 Nov 2018

Org. Chem. Front., 2019,6, 32-35

Transition metal-free base-promoted arylation of sulfenate anions with diaryliodonium salts

L. Wang, M. Chen and J. Zhang, Org. Chem. Front., 2019, 6, 32 DOI: 10.1039/C8QO00914G

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