Enantioselective Desymmetrization of Phosphinic Acids via Cu-Catalyzed O-Arylation

被引:0
|
作者
Yan, Ming [1 ]
Zou, Jia-wei [2 ]
Fang, Dong-mei [1 ]
Zhang, Shi-qi [1 ]
Cui, Xin [1 ]
Tang, Zhuo [1 ]
Li, Guang-xun [1 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Biol, Biol Resources Applying Ctr, Chengdu 610041, Sichuan, Peoples R China
[2] Leshan Normal Univ, Dept New Energy Mat & Chem, Leshan 614004, Sichuan, Peoples R China
来源
ACS CATALYSIS | 2025年 / 15卷 / 06期
关键词
Enantioselective desymmetrization; Copper catalysis; Chiral phosphorus compounds; Diaryliodonium salt; Phosphinic acid; EFFICIENT ASYMMETRIC-SYNTHESIS; P-STEREOGENIC PHOSPHINAMIDES; CHIRAL PHOSPHINES; P(O)-OH COMPOUNDS; OXIDES; ACCESS; LIGANDS; AMINOPHOSPHINES; CYCLIZATION; INHIBITORS;
D O I
10.1021/acscatal.5c00439
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Enantioselective desymmetrization of phosphinic acid with two completely different carbon substituents on the P atom is an efficient way to obtain chiral P(V) compounds with high structural diversity. Herein, we reported a Cu-catalyzed asymmetric arylation of phosphinic acid, which turns the P-center to be a versatile electrophile for obtaining a series of chiral P(V) compounds, including phosphinates, phosphinamides, and tertiary phosphine oxides, in good yields and high enantioselectivities.
引用
收藏
页码:4719 / 4725
页数:7
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