Stereoselective Catalytic Synthesis of P-Stereogenic Oxides via Hydrogenative Kinetic Resolution

被引:25
作者
Fernandez-Perez, Hector [2 ,3 ]
Vidal-Ferran, Anton [1 ,2 ,3 ]
机构
[1] ICREA, P Lluis Co 23, Barcelona 08010, Spain
[2] ICIQ, Av Paisos Catalans 16, Tarragona 43007, Spain
[3] BIST, Av Paisos Catalans 16, Tarragona 43007, Spain
关键词
ASYMMETRIC HYDROGENATION; PHOSPHINE OXIDES; ENANTIOSELECTIVE SYNTHESIS; OP LIGANDS; ACCESS; DESYMMETRIZATION; ARYLATION; OLEFIN;
D O I
10.1021/acs.orglett.9b02606
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly stereoselective catalytic method for the preparation of structurally diverse P-stereogenic oxides has been developed. The approach relies on the ability of rhodium complexes derived from an enantiopure P-OP ligand to kinetically resolve racemic alpha,beta-unsaturated phosphane oxides by hydrogenation of the C=C motif and formation of highly enantioenriched (or even enantiopure) P-stereogenic oxides. The practicality of the methodology has been demonstrated by the preparation of potentially functional P-chiral molecules for catalytic enantioselective synthesis.
引用
收藏
页码:7019 / 7023
页数:5
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