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◆ Organic Letters2025-11-13· Sulfonium

Sulfonium Salt-Mediated Bisthiolation of Terminal Alkynes to Access Symmetrical and Nonsymmetrical <i>Z-</i> 1,2 <i>-</i> Dithioalkenes

Sha Peng, Xiang-Qin Xu, Ding Luo, Limei Duan, Li‐Hua Yang, Long‐Yong Xie

原始摘要(英文原文)· Original abstract
In this study, we report an efficient one-pot bisthiolation reaction of terminal alkynes, which enables the regio- and stereoselective synthesis of diverse symmetrical and nonsymmetrical ( Z )-1,2-dithioalkenes with wide substrate scope and excellent functional group compatibility. Mechanistic investigations reveal that the reaction is initiated by in situ-generated alkynyl sulfonium salts, formed from terminal alkynes, sulfoxides, and triflic anhydride (Tf 2 O). Gram-scale synthesis and late-stage functionalization further underscore the application of this method in organic synthesis.
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Sulfonium Salt-Mediated Bisthiolation of Terminal Alkynes to Access Symmetrical and Nonsymmetrical <i>Z-</i> 1,2 <i>-</i> Dithioalkenes — 科研速览 Science Skim