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Photoinduced metal-free cascade silylation/cyclization of alkynes/alkynones with hydrosilanes to access 3-silylated benzothiophenes and thioflavones.

Created on 08 Oct 2026

Authors

Yunfei Tian, Weijun Fu, Zhiqiang Wang, Xi Li, Jinzhao Ren, Yukai Liu, Luping Zheng, Kai Sun, Zejiang Li

Published in

Organic & biomolecular chemistry. Oct 08, 2026. Epub Oct 08, 2026.

Abstract

A metal-free photocatalytic method for the synthesis of silylated thioflavones and benzothiophenes has been established through cascade silylation/cyclization of alkynes/alkynones with hydrosilanes. This transformation features mild reaction conditions, excellent functional group compatibility, and broad substrate scope. Moreover, this method can be readily applied to the late-stage silylation of structurally complex bioactive molecules, thus offering potential applications for pharmaceutical research. Mechanistic investigations indicate that this reaction proceeds through a radical pathway.

PMID:
42845009
Bibliographic data and abstract were imported from PubMed on 08 Oct 2026.

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