Visible-Light-Mediated Metal-Free Desulfonylative Silylation for Alkenyl and Alkynylsilanes with Silacarboxylic Acids

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Authors: Zhao‐Zhao Zhou
Cited by: 1
References: 79

Abstract

High Resolution Image Download MS PowerPoint Slide Herein, we report a brand-new example of visible-light-mediated desulfonylative silylation between silacarboxylic acids and α,β-unsaturated aryl sulfones. Valuable alkenyl and alkynylsilane skeletons had been efficiently synthesized, and abundant substrate sources made the reaction more alternative and widely applicable, simultaneously avoiding limitations from conventional methodologies. Meanwhile, the gram-scale reaction with a hydroxyl-containing substrate and successful involvement of dehydrocholic acid derivatives further demonstrated the practicality of this desulfonylative silylation process. Mechanically, a cascade process with silyl radical addition and PhSO 2 – elimination was proposed.

Fields of Study & Subjects

Organoboron and organosilicon chemistry Radical Photochemical Reactions Catalytic Cross-Coupling Reactions

Publication details

Journal / source
ACS Omega
Publisher
American Chemical Society (ACS)
Volume
11
Issue
14
Pages
21824–21835
Publication date
31 March 2026
Language
EN