Lewis Acid-Mediated Deoxygenative Synthesis of Trivalent Sterically Hindered Phosphines from Aldehydes

The efficient synthesis of trisubstituted trivalent phosphines remains challenging. Herein, we report a novel approach for rapid construction of these compounds from aldehydes under Lewis acid-mediated conditions. By using sterically hindered disubstituted phosphines, aldehydes can undergo a deoxygenative reaction to afford trivalent phosphorus compounds. This modular and practical method is characterized by operational simplicity, a broad substrate scope, and excellent functional group tolerance, which holds great potential for applications in organic synthesis.

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Publication Details

Journal
Organic Letters
Published
2025-05-29
DOI
https://doi.org/10.1021/acs.orglett.5c01581
Citations
4
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
3.74

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article

Lewis Acid-Mediated Deoxygenative Synthesis of Trivalent Sterically Hindered Phosphines from Aldehydes

Tao Xu, Wei Zhong, Xiaoqiang Wu, Abuduwaili Alimu
4 citations
Organic Letters
Organophosphorus compounds synthesis
3.74
article

Lewis Acid-Mediated Deoxygenative Synthesis of Trivalent Sterically Hindered Phosphines from Aldehydes

Tao Xu, Wei Zhong, Xiaoqiang Wu, Abuduwaili Alimu
article en
4 citations

Abstract

The efficient synthesis of trisubstituted trivalent phosphines remains challenging. Herein, we report a novel approach for rapid construction of these compounds from aldehydes under Lewis acid-mediated conditions. By using sterically hindered disubstituted phosphines, aldehydes can undergo a deoxygenative reaction to afford trivalent phosphorus compounds. This modular and practical method is characterized by operational simplicity, a broad substrate scope, and excellent functional group tolerance, which holds great potential for applications in organic synthesis.

Organic LettersVol. 27(23)
Tongji University (CN), Jiaxing University (CN)
National Natural Science Foundation of China, Jiaxing University, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 7%
Organophosphorus compounds synthesis
3.74
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