Visible-light-induced radical 1,3-hydrosulfonylation of allylketones with sulfonyl chlorides

A radical 1,3-hydrosulfonylation of allylketones with sulfonyl chlorides <i>via</i> 1,2-carbonyl migration has been achieved under visible-light-irradiation. This reaction proceeds efficiently under mild conditions and exhibits broad substrate scope and excellent functional group tolerance. The synthetic utility of this method is demonstrated by scale-up synthesis and late-stage modification of biologically relevant molecules.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc01285f
Citations
4
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
3.74

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article

Visible-light-induced radical 1,3-hydrosulfonylation of allylketones with sulfonyl chlorides

Guodong Zhang, Xin Zheng, Xinlong Zhang, Tuanli Yao et al.
4 citations
Chemical Communications
Sulfur-Based Synthesis Techniques
3.74
article

Visible-light-induced radical 1,3-hydrosulfonylation of allylketones with sulfonyl chlorides

Guodong Zhang, Xin Zheng, Xinlong Zhang, Tuanli Yao, Xinglong Han, Qin Zhang, Xiang Li
article en
4 citations

Abstract

A radical 1,3-hydrosulfonylation of allylketones with sulfonyl chlorides <i>via</i> 1,2-carbonyl migration has been achieved under visible-light-irradiation. This reaction proceeds efficiently under mild conditions and exhibits broad substrate scope and excellent functional group tolerance. The synthetic utility of this method is demonstrated by scale-up synthesis and late-stage modification of biologically relevant molecules.

Chemical CommunicationsVol. 61(54)
Shaanxi University of Science and Technology (CN), Yangzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 7%
Sulfur-Based Synthesis Techniques
3.74
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