Affiliation:
1. State Key Laboratory of Medical Chemical Biology College of Pharmacy Nankai University 38 Tongyan Road, Jinnan District Tianjin 300350 P. R. China
Abstract
AbstractTransition‐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.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Cited by
2 articles.
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