Recent Advances on Chiral Catalysts for Asymmetric Hydrogenation of C=C, C=N and C=O Bonds

被引:14
|
作者
Drommi, Dario [1 ]
Arena, Carmela G. [1 ]
机构
[1] Univ Messina, Dipartimento Sci Chim Biol Farmaceut & Ambientali, Viale F Stagno DAlcontres 31, I-98166 Vill S Agata Messina, Italy
关键词
Asymmetric hydrogenation; homogeneous catalysis; enantiopure compounds; organic synthesis; metal complex; chiral ligands; HIGHLY ENANTIOSELECTIVE HYDROGENATION; PHOSPHINE-PHOSPHORAMIDITE LIGANDS; MINIMALLY FUNCTIONALIZED OLEFINS; BINOL-DERIVED PHOSPHORAMIDITES; SUBSTITUTED CINNAMIC-ACIDS; TERT-ALKYL KETONES; N-ARYL IMINES; P-OP LIGANDS; R-SMS-PHOS; IRIDIUM-CATALYSTS;
D O I
10.2174/1385272820666160620111858
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The asymmetric hydrogenation of C=C, C=N and C=O bonds catalyzed by chiralligand modified transition metal complexes is a very important process for the organic synthesis and fine chemical production. A large number of hydrogenation chiral catalysts mainly based on transition metals such as rhodium, ruthenium and iridium have been successfully developed. Even though outstanding results have been achieved in this area, so far relatively few catalysts for asymmetric hydrogenation have been applied to fine chemical industry [5-6]. Thus, many efforts are being made to rationally design highly active catalysts with a broad substrate scope. In the last few years, less expensive catalysts based on transition metals such as cobalt, copper, iron and palladium have afforded promising results. This review reports on the most relevant chiral catalysts for asymmetric hydrogenation of C=C, C=N and C=O bonds that were published from 2005 up today.
引用
收藏
页码:2552 / 2590
页数:39
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