Electrochemically driven hydrophosphination of alkenes and alkynes with diphenylphosphine

We herein report a mild, efficient, and sustainable electrochemical method for the hydrophosphination of a broad range of alkynes and alkenes with diphenylphosphine. This transition metal-free and additive-free protocol exhibits wide substrate compatibility, delivering the corresponding vinylphosphines and alkylphosphines in good to excellent yields. Moreover, the method is scalable to gram-scale synthesis and enables further transformations in an efficient manner. Mechanistic studies suggest that the reaction proceeds <i>via</i> electrochemically induced addition of diphenylphosphinyl radicals to alkynes or alkenes.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00764j
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

Electrochemically driven hydrophosphination of alkenes and alkynes with diphenylphosphine

Fan Zhao, Hui Qiu, Fei Xue, Mengtao Ma et al.
Organic & Biomolecular Chemistry
Asymmetric Hydrogenation and Catalysis
article

Electrochemically driven hydrophosphination of alkenes and alkynes with diphenylphosphine

Fan Zhao, Hui Qiu, Fei Xue, Mengtao Ma, Xichen Zhang
article en

Abstract

We herein report a mild, efficient, and sustainable electrochemical method for the hydrophosphination of a broad range of alkynes and alkenes with diphenylphosphine. This transition metal-free and additive-free protocol exhibits wide substrate compatibility, delivering the corresponding vinylphosphines and alkylphosphines in good to excellent yields. Moreover, the method is scalable to gram-scale synthesis and enables further transformations in an efficient manner. Mechanistic studies suggest that the reaction proceeds <i>via</i> electrochemically induced addition of diphenylphosphinyl radicals to alkynes or alkenes.

Organic & Biomolecular ChemistryVol. 23(27)
Nanjing Forestry University (CN)
Responsible consumption and production
Openalex Percentile: Top 88%
Asymmetric Hydrogenation and Catalysis
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