Demonstrates regio- and stereoselective aminosulfonylation in alkynes, suggesting valuable applications in organic synthesis.
In this study, a practical and efficient one-pot sulfonium salt-mediated regio- and stereoselective aminosulfonylation of alkynes with sulfinates and azoles has been established. This method enables the synthesis of structurally diverse N-heterocycle-containing (Z)-vinyl sulfones, featuring a broad substrate scope and excellent functional group tolerance. Notably, gram-scale synthesis, product derivatization, and late-stage functionalization further validate the synthetic utility of this protocol, thereby rendering it highly valuable for applications in organic synthesis and medicinal chemistry.
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Peng et al. (2026) studied this question.
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