Photoinduced Deacylative Phosphorylation of Unstrained Ketones

The photoinduced deacylative transformation of ketones represents a powerful strategy for forming chemical bonds and developing innovative reactions. However, its potential application in deacylative phosphorylation remains unexplored. Herein, we report a metal-free, light-driven deacylative phosphorylation of unstrained ketones with diarylchlorophosphines, enabling the efficient synthesis of a wide variety of symmetrical and unsymmetrical tertiary phosphines. This method features mild conditions, operational simplicity, and broad substrate scope.

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Publication Details

Journal
Organic Letters
Published
2026-03-31
DOI
https://doi.org/10.1021/acs.orglett.6c00848
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoinduced Deacylative Phosphorylation of Unstrained Ketones

Long Zhang, Jimmy C. Yu, Xiao‐Qiang Hu, Xiaoyun Hu et al.
Organic Letters
Organophosphorus compounds synthesis
article

Photoinduced Deacylative Phosphorylation of Unstrained Ketones

Long Zhang, Jimmy C. Yu, Xiao‐Qiang Hu, Xiaoyun Hu, Linghe Li, Yuan Chen, Xiying Lai
article en

Abstract

The photoinduced deacylative transformation of ketones represents a powerful strategy for forming chemical bonds and developing innovative reactions. However, its potential application in deacylative phosphorylation remains unexplored. Herein, we report a metal-free, light-driven deacylative phosphorylation of unstrained ketones with diarylchlorophosphines, enabling the efficient synthesis of a wide variety of symmetrical and unsymmetrical tertiary phosphines. This method features mild conditions, operational simplicity, and broad substrate scope.

Organic LettersVol. 28(14)
Minzu University of China (CN), Kanto Chemical (Japan) (JP), Ministry of Education (PT)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province, South-Central University for Nationalities
Industry, innovation and infrastructure
Openalex Percentile: Top 27%
Organophosphorus compounds synthesis
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