Issue 14, 2016

Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction

Abstract

A novel strategy for installation of a sulfonyl fragment into arenes has been accomplished via an iron-catalyzed radical coupling reaction. Arene radicals derived from diaryliodoniums via single electron transfer reaction combine with sulfoxylate anion radicals readily generated from commercially available rongalite (HOCH2SO2Na·2H2O) to afford arylsulfinates efficiently at room temperature. In this protocol, a broad range of functional groups are tolerated to give products in good yields.

Graphical abstract: Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction

Supplementary files

Article information

Article type
Communication
Submitted
28 Nov 2015
Accepted
11 Jan 2016
First published
11 Jan 2016

Chem. Commun., 2016,52, 2980-2983

Author version available

Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction

W. Zhang and M. Luo, Chem. Commun., 2016, 52, 2980 DOI: 10.1039/C5CC09830K

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