Visible-Light-Enabled Fluorosulfonylalkynylation of Alkenes

A visible-light-enabled fluorosulfonylalkynylation of alkenes has been developed using alkynyl sulfonyl fluorides as bifunctional reagents under catalytic aryl diazonium activation. This photocatalyst- and oxidant-free protocol affords diverse 1-sulfonyl fluoride-2-alkynyl adducts in good yields with excellent chemoselectivity and a broad scope, enabling late-stage diversification while installing a SuFEx-ready sulfonyl fluoride and a versatile alkyne in one step.

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Publication Details

Journal
Organic Letters
Published
2026-01-13
DOI
https://doi.org/10.1021/acs.orglett.5c05131
Primary Topic
Click Chemistry and Applications
Type
article
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article

Visible-Light-Enabled Fluorosulfonylalkynylation of Alkenes

Hai‐Tao Zhu, Yucai Tang, Jiaming Huang, Weimin He et al.
Organic Letters
Click Chemistry and Applications
article

Visible-Light-Enabled Fluorosulfonylalkynylation of Alkenes

Hai‐Tao Zhu, Yucai Tang, Jiaming Huang, Weimin He, Qiangsheng He, Jiale Liu, Yonghao Li, Yao-Dan Xu, Jun-Ji Lu
article en

Abstract

A visible-light-enabled fluorosulfonylalkynylation of alkenes has been developed using alkynyl sulfonyl fluorides as bifunctional reagents under catalytic aryl diazonium activation. This photocatalyst- and oxidant-free protocol affords diverse 1-sulfonyl fluoride-2-alkynyl adducts in good yields with excellent chemoselectivity and a broad scope, enabling late-stage diversification while installing a SuFEx-ready sulfonyl fluoride and a versatile alkyne in one step.

Organic LettersVol. 28(3)
Hunan University of Arts and Science (CN), Baoji University of Arts and Sciences (CN), Material (Belgium) (BE), Nomura Plating (Japan) (JP), University of South China (CN)
Openalex Percentile: Top 90%
Click Chemistry and Applications
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Visible-Light-Enabled Fluorosulfonylalkynylation of Alkenes — Hai‐Tao Zhu, Yucai Tang, et al. · Organic Letters (2026) | TGRS Research Map | TGRS