Synthesis of 4-Sulfenyl-Isocoumarins via Thio-Annulation of 2-Alkynyl-benzonate with RSCl: In Situ Preparation using Disulfides and HCl/HNO3

Abstract We have developed a novel and metal-free method to construct the derivatives of 4-sulfenyl isocoumarins via thio-annulation of 2-alkynyl benzoates with sulfenyl chlorides which is in situ prepared by disulfides and HCl/HNO3. The reaction shows high functional group tolerance and can be scaled up to the gram-scale with less loss in yield. Both sulfide groups of the disulfide reagent were used in the reaction.

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Publication Details

Journal
Synthesis
Published
2026-02-02
DOI
https://doi.org/10.1055/a-2802-6034
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
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article

Synthesis of 4-Sulfenyl-Isocoumarins via Thio-Annulation of 2-Alkynyl-benzonate with RSCl: In Situ Preparation using Disulfides and HCl/HNO3

Zhixiang Yao, Y. X. Yang, Hui Su, Li Lu Ting et al.
Synthesis
Sulfur-Based Synthesis Techniques
article

Synthesis of 4-Sulfenyl-Isocoumarins via Thio-Annulation of 2-Alkynyl-benzonate with RSCl: In Situ Preparation using Disulfides and HCl/HNO3

Zhixiang Yao, Y. X. Yang, Hui Su, Li Lu Ting, xiaocheng huang
article en

Abstract

Abstract We have developed a novel and metal-free method to construct the derivatives of 4-sulfenyl isocoumarins via thio-annulation of 2-alkynyl benzoates with sulfenyl chlorides which is in situ prepared by disulfides and HCl/HNO3. The reaction shows high functional group tolerance and can be scaled up to the gram-scale with less loss in yield. Both sulfide groups of the disulfide reagent were used in the reaction.

Synthesis
Guangxi University of Science and Technology (CN)
Clean water and sanitation
Openalex Percentile: Top 68%
Sulfur-Based Synthesis Techniques
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