Issue 3, 2022

A Ni(ii)-catalyzed reductive cross-coupling reaction of oxalates and thiosulfonates/selenosulfonates

Abstract

A Ni(II)-catalyzed reductive cross-coupling reaction of oxalates and thiosulfonates/selenosulfonates to synthesize benzylic sulfides/selenides under mild conditions is developed. The oxalates prepared from the corresponding alcohols are used as carbon radical precursors to participate in the reaction. This strategy has the advantages of easy substrate availability and mild conditions, and provides a new method for the preparation of unsymmetrical sulfides/selenides with good functional group tolerance.

Graphical abstract: A Ni(ii)-catalyzed reductive cross-coupling reaction of oxalates and thiosulfonates/selenosulfonates

Supplementary files

Article information

Article type
Research Article
Submitted
26 Oct 2021
Accepted
11 Dec 2021
First published
15 Dec 2021

Org. Chem. Front., 2022,9, 731-736

A Ni(II)-catalyzed reductive cross-coupling reaction of oxalates and thiosulfonates/selenosulfonates

Y. Chen, F. Wang, B. Liu, W. Rao and S. Wang, Org. Chem. Front., 2022, 9, 731 DOI: 10.1039/D1QO01614H

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