Synthesis of Vinyl Sulfones and Benzoxathiins via Base‐Catalyzed Reactions of <i>o</i>‐Hydroxyaryl Thiosulfonates and Ynones

Abstract The cyclization reaction and hydrosulfonylation reaction of ynones have been simultaneously realized through a single operation. Under the mediation of cesium carbonate, different S ‐( α ‐hydroxyaryl) aryl thiosulfonates reacted with various ynones to produce functionalized vinyl sulfones in 37%–83% yields with E ‐selectivity. At the same time, a variety of benzoxathiins were formed in 42%–97% yields.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-04
DOI
https://doi.org/10.1002/adsc.202400456
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.25

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article

Synthesis of Vinyl Sulfones and Benzoxathiins via Base‐Catalyzed Reactions of o‐Hydroxyaryl Thiosulfonates and Ynones

Lin He, Zhihua Cai, Jinyun Luo, Guangfen Du et al.
1 citations
Advanced Synthesis & Catalysis
Sulfur-Based Synthesis Techniques
0.25
article

Synthesis of Vinyl Sulfones and Benzoxathiins via Base‐Catalyzed Reactions of o‐Hydroxyaryl Thiosulfonates and Ynones

Lin He, Zhihua Cai, Jinyun Luo, Guangfen Du, Delin Tang, Fang Zhang
article en
1 citations

Abstract

Abstract The cyclization reaction and hydrosulfonylation reaction of ynones have been simultaneously realized through a single operation. Under the mediation of cesium carbonate, different S ‐( α ‐hydroxyaryl) aryl thiosulfonates reacted with various ynones to produce functionalized vinyl sulfones in 37%–83% yields with E ‐selectivity. At the same time, a variety of benzoxathiins were formed in 42%–97% yields.

Advanced Synthesis & CatalysisVol. 367(3)
Shihezi University (CN)
National Natural Science Foundation of China, Shihezi University
Openalex Percentile: Top 48%
Sulfur-Based Synthesis Techniques
0.25
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