立体中心
磷化氢
对映选择合成
芳基
化学
催化作用
动力学分辨率
配体(生物化学)
铜
组合化学
药物化学
有机化学
生物化学
受体
烷基
作者
Jie Kang,Kang Ding,Si‐Mu Ren,Bo Su
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-04-14
卷期号:62 (25): e202301628-e202301628
被引量:49
标识
DOI:10.1002/anie.202301628
摘要
Abstract Transition‐metal‐catalyzed enantioselective P−C cross‐coupling of secondary phosphine oxides (SPOs) is an attractive method for synthesizing P ‐stereogenic phosphorus compounds, but the development of such a dynamic kinetic asymmetric process remains a considerable challenge. Here we report an unprecedented highly enantioselective dynamic kinetic intermolecular P−C coupling of SPOs and aryl iodides catalyzed by copper complexes ligated by a finely modified chiral 1,2‐diamine ligand. The reaction tolerates a wide range of SPOs and aryl iodides, affording P ‐stereogenic tertiary phosphine oxides (TPOs) in high yields and with good enantioselectivity (average 89.2 % ee). The resulting enantioenriched TPOs were transformed into structurally diverse P ‐chiral scaffolds, which are highly valuable as ligands and catalysts in asymmetric synthesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI