Cyclic β-iminophosphine:: New P-stereogenic ligand for the asymmetric catalysed hydrogenation of ketones

被引:5
|
作者
Christ, ML
Zablocka, M
Spencer, S
Lavender, RJ
Lemaire, M
Majoral, JP
机构
[1] Univ Lyon 1, CNRS, Lab Catalyse & Synthese Organ, F-69622 Villeurbanne, France
[2] Polish Acad Sci, Ctr Mol & Macromol Studies, PL-90363 Lodz, Poland
[3] CNRS, Chim Coordinat Lab, F-31077 Toulouse, France
关键词
asymmetric hydrogenation; P; N-chiral ligands; chiral ligands synergy; ruthenium catalysts;
D O I
10.1016/j.molcata.2005.09.043
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
A novel type of asymmetric C=O hydrogenation catalysts based on chiral beta-iminophosphine rhodium and ruthenium complexes was developed. The chirality of the ligand is centered on the phosphorus atom which can induce moderate enantioselectivity. A synergetic effect on both activity and enantioselectivity is observed when amines are introduced as co-ligands. Acetophenone is thus completely hydrogenated with ee values up to 68%. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 216
页数:7
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