Issue 11, 2025

Cascade reaction of α-aryl vinyl and propargyl sulfonium salts with carbon nucleophiles: synthesis of functionalized benzyl and homoallyl thioethers

Abstract

We report a cascade reaction of α-aryl vinyl and propargyl sulfonium salts with C-nucleophiles, resulting in the formation of functionalized benzyl and homoallyl thioethers, respectively, in good yields. In this novel reaction, a vinyl sulfonium derivative undergoes Michael addition with a C-nucleophile followed by [2,3]-sigmatropic rearrangement. This domino reaction is very general and takes place readily under mild conditions.

Graphical abstract: Cascade reaction of α-aryl vinyl and propargyl sulfonium salts with carbon nucleophiles: synthesis of functionalized benzyl and homoallyl thioethers

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Article information

Article type
Communication
Submitted
17 Jan 2025
Accepted
05 Feb 2025
First published
06 Feb 2025

Org. Biomol. Chem., 2025,23, 2610-2614

Cascade reaction of α-aryl vinyl and propargyl sulfonium salts with carbon nucleophiles: synthesis of functionalized benzyl and homoallyl thioethers

V. M. Awchar and S. Baskaran, Org. Biomol. Chem., 2025, 23, 2610 DOI: 10.1039/D5OB00087D

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