Electroreduction cross-coupling of thiosulfonates with (hetero)aryl boronic acids to access thioethers

Abstract

Herein, we present a robust electrochemically driven, 1-iodonaphthalene-enabled cross-coupling of thiosulfonates with arylboronic acids for the synthesis of thioether molecules. This reaction is characterized by exceptional selectivity, gentle reaction conditions, a broad substrate scope, and significant functional group tolerance that extends to late-stage modifications of biologically relevant molecules.

Graphical abstract: Electroreduction cross-coupling of thiosulfonates with (hetero)aryl boronic acids to access thioethers

Supplementary files

Article information

Article type
Communication
Submitted
04 Oct 2025
Accepted
16 Nov 2025
First published
01 Dec 2025

Chem. Commun., 2026, Advance Article

Electroreduction cross-coupling of thiosulfonates with (hetero)aryl boronic acids to access thioethers

Y. Zhou, J. Lei, M. Chen, C. Zhang, Z. Zhao and L. Gu, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D5CC05687J

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