Sulfonium Salt-Mediated Difunctionalization of Alkynes for Access to <i>Z</i>-Alkenyl Phosphorothioates and Selenophosphates

In this work, we present a practical and efficient one-pot sulfonium salt-mediated difunctionalization reaction of alkynes. This method facilitates the diverse synthesis of various alkenyl phosphorthioates and selenophosphates in acceptable yields. Importantly, the reaction is completely regio- and stereoselective, producing absolutely <i>Z</i>-configured alkenylated phosphorothioates and selenophosphates with a broad substrate scope and high functional group tolerance.

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Publication Details

Journal
Organic Letters
Published
2025-07-20
DOI
https://doi.org/10.1021/acs.orglett.5c02426
Citations
9
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
8.42

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article

Sulfonium Salt-Mediated Difunctionalization of Alkynes for Access to Z-Alkenyl Phosphorothioates and Selenophosphates

Li Tang, Long‐Yong Xie, Ni-Dan Meng, Sha Peng et al.
9 citations
Organic Letters
Sulfur-Based Synthesis Techniques
8.42
article

Sulfonium Salt-Mediated Difunctionalization of Alkynes for Access to Z-Alkenyl Phosphorothioates and Selenophosphates

Li Tang, Long‐Yong Xie, Ni-Dan Meng, Sha Peng, Xinhua Xu, Li‐Hua Yang
article en
9 citations

Abstract

In this work, we present a practical and efficient one-pot sulfonium salt-mediated difunctionalization reaction of alkynes. This method facilitates the diverse synthesis of various alkenyl phosphorthioates and selenophosphates in acceptable yields. Importantly, the reaction is completely regio- and stereoselective, producing absolutely <i>Z</i>-configured alkenylated phosphorothioates and selenophosphates with a broad substrate scope and high functional group tolerance.

Organic LettersVol. 27(30)
Hunan University of Science and Engineering (CN), Bioengineering Center (RU)
National Natural Science Foundation of China, Scientific Research Foundation of Hunan Provincial Education Department
Openalex Percentile: Top 2%
Sulfur-Based Synthesis Techniques
8.42
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