Issue 50, 2023

Iodine-mediated photoinduced tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates

Abstract

An efficient transition-metal free iodine-mediated tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates under visible light irradiation has been developed. This photochemical protocol offers broad substrate scope of 1,2-bissulfonylethenes with high functional group tolerance and good yields under mild reaction conditions. In addition, it was found that β-sulfinyl alkenylsulfones can be obtained in the absence of base. It is proposed that the reactions proceed via sulfonyl and sulfinyl radicals.

Graphical abstract: Iodine-mediated photoinduced tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates

Supplementary files

Article information

Article type
Communication
Submitted
25 Apr 2023
Accepted
22 May 2023
First published
23 May 2023
This article is Open Access
Creative Commons BY license

Chem. Commun., 2023,59, 7767-7770

Iodine-mediated photoinduced tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates

M. B. Reddy and E. M. McGarrigle, Chem. Commun., 2023, 59, 7767 DOI: 10.1039/D3CC02011H

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