The one-step formation of four chemical bonds toward dithiophosphinates <i>via</i> a multicomponent reaction

A multicomponent reaction involving diphenylphosphine, S<sub>8</sub>, and alcohols has been developed for the efficient dehydrative synthesis of dithiophosphinates. This method enables the one-pot construction of four chemical bonds (S-C-PS), delivering the target products with exclusive selectivity. A broad substrate scope, including a variety of allylic alcohols, benzyl alcohols, and even aliphatic alcohols, can be tolerated.

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Publication Details

Journal
Chemical Communications
Published
2025-12-22
DOI
https://doi.org/10.1039/d5cc06363a
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

The one-step formation of four chemical bonds toward dithiophosphinates via a multicomponent reaction

Tianyuan Li
Chemical Communications
Sulfur-Based Synthesis Techniques
article

The one-step formation of four chemical bonds toward dithiophosphinates via a multicomponent reaction

Tianyuan Li
article en

Abstract

A multicomponent reaction involving diphenylphosphine, S<sub>8</sub>, and alcohols has been developed for the efficient dehydrative synthesis of dithiophosphinates. This method enables the one-pot construction of four chemical bonds (S-C-PS), delivering the target products with exclusive selectivity. A broad substrate scope, including a variety of allylic alcohols, benzyl alcohols, and even aliphatic alcohols, can be tolerated.

Chemical CommunicationsVol. 62(7)
Xinyang Normal University (CN)
Openalex Percentile: Top 34%
Sulfur-Based Synthesis Techniques
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The one-step formation of four chemical bonds toward dithiophosphinates <i>via</i> a multicomponent reaction — Tianyuan Li · Chemical Communications (2025) | TGRS Research Map | TGRS