Asymmetric Hydrophosphination of Quinolinones and Chromones Catalyzed by Chiral Phosphoric Acid

Here, we report the first highly efficient and enantioselective hydrophosphination of quinolinones and chromones catalyzed by chiral phosphoric acids, affording C2-stereogenic phosphorus derivatives in good yields and high enantioselectivities. Notably, these products serve as versatile synthetic intermediates that can be readily elaborated to a range of valuable phosphorus-containing molecules.

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Publication Details

Journal
Organic Letters
Published
2026-07-02
DOI
https://doi.org/10.1021/acs.orglett.6c02232
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Asymmetric Hydrophosphination of Quinolinones and Chromones Catalyzed by Chiral Phosphoric Acid

Guiyong Wang, Zhifeng Ma, Yafei Guo, B Q Fan et al.
Organic Letters
Organophosphorus compounds synthesis
article

Asymmetric Hydrophosphination of Quinolinones and Chromones Catalyzed by Chiral Phosphoric Acid

Guiyong Wang, Zhifeng Ma, Yafei Guo, B Q Fan, Jiuling Li, Rui Yang, Shengrong Chen
article en

Abstract

Here, we report the first highly efficient and enantioselective hydrophosphination of quinolinones and chromones catalyzed by chiral phosphoric acids, affording C2-stereogenic phosphorus derivatives in good yields and high enantioselectivities. Notably, these products serve as versatile synthetic intermediates that can be readily elaborated to a range of valuable phosphorus-containing molecules.

Organic Letters
Minzu University of China (CN)
National Natural Science Foundation of China, Yunnan Provincial Department of Education, Yunnan Provincial Science and Technology Department
Openalex Percentile: Top 14%
Organophosphorus compounds synthesis
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