Asymmetric hydrosilylation, transfer hydrogenation and hydrogenation of ketones catalyzed by iridium complexes

被引:313
作者
Malacea, Raluca [1 ]
Poli, Rinaldo [1 ]
Manoury, Eric [1 ]
机构
[1] Univ Toulouse, UPS, INP, CNRS,LCC, F-31077 Toulouse, France
关键词
Iridium; Chiral alcohols; Asymmetric hydrosilylation; Asymmetric transfer hydrogenation; Asymmetric hydrogenation; Mechanisms; Iridium hydrides; HYDRIDE TRANSFER REDUCTION; AROMATIC KETONES; ENANTIOSELECTIVE HYDROGENATION; DIFERROCENYL DICHALCOGENIDES; CHIRAL LIGANDS; SELECTIVE HYDROGENATION; KINETIC RESOLUTION; RHODIUM(I) COMPLEX; EFFICIENT IRIDIUM; C=O HYDROGENATION;
D O I
10.1016/j.ccr.2009.09.033
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Iridium-based asymmetric reduction of ketones to chiral enantiomerically enriched alcohols has recently attracted attention by a number of research groups and interest in this area is growing. This review presents the different catalytic systems based on iridium complexes that have been used in asymmetric hydrosilylation, in asymmetric transfer hydrogenation (ATH) with alcohols or formic acid derivatives as reducing agents, and in asymmetric hydrogenation (H-2 as reducing agent). A large variety of chiral ligands of various denticities and bearing various combination of coordinating atoms (N, P, S, O, C, ...) have been used and will be presented. The last part critically reviews the mechanistic understanding of all the above transformations with specific reference to iridium catalysts. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:729 / 752
页数:24
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