Visible Light‐Induced Arylsulfonylation/Cyclization Reactions for the Synthesis of Thiochromane 1,1‐dioxide

Simple operation, easily accessible starting materials, and short syntheses of the privileged scaffold thiochromane 1,1-dioxide that widely exist in bioactive molecules was achieved by photocatalytic divergent cyclization of α-allyl-β-ketosulfones with arylsulfonyl chlorides. Optimization and scope and limitations of this short and general pathway are described. The methodology provides an efficient strategy for the construction of a wide variety of thiochromane 1,1-dioxide derivatives.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2025-03-11
DOI
https://doi.org/10.1002/asia.202401940
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Visible Light‐Induced Arylsulfonylation/Cyclization Reactions for the Synthesis of Thiochromane 1,1‐dioxide

Na Ma, Fei Gao, Shan Li, Yang Liu
1 citations
Chemistry - An Asian Journal
Sulfur-Based Synthesis Techniques
0.94
article

Visible Light‐Induced Arylsulfonylation/Cyclization Reactions for the Synthesis of Thiochromane 1,1‐dioxide

Na Ma, Fei Gao, Shan Li, Yang Liu
article en
1 citations

Abstract

Simple operation, easily accessible starting materials, and short syntheses of the privileged scaffold thiochromane 1,1-dioxide that widely exist in bioactive molecules was achieved by photocatalytic divergent cyclization of α-allyl-β-ketosulfones with arylsulfonyl chlorides. Optimization and scope and limitations of this short and general pathway are described. The methodology provides an efficient strategy for the construction of a wide variety of thiochromane 1,1-dioxide derivatives.

Chemistry - An Asian JournalVol. 20(10)
Shanghai University (CN), University of Science and Technology (YE), University of Shanghai for Science and Technology (CN), Liaocheng University (CN), Shanghai Research Institute of Chemical Industry (CN), People's Liberation Army 401 Hospital (CN)
Openalex Percentile: Top 28%
Sulfur-Based Synthesis Techniques
0.94
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