Development of iridium-catalyzed asymmetric hydrogenation: New catalysts, new substrate scope

被引:42
作者
Cadu, Alban [1 ]
Andersson, Pher G. [1 ,2 ]
机构
[1] Uppsala Univ, Dept Biochem & Organ Chem, SE-75123 Uppsala, Sweden
[2] Univ KwaZulu Natal, Sch Chem, Durban, South Africa
关键词
Asymmetric catalysis; Iridium; Hydrogenation; Alkenes; OPTICALLY-ACTIVE 2-(TRIFLUOROMETHYL)ALKAN-1-OLS; ENANTIOSELECTIVE HYDROGENATION; CYCLIC SULFONES; OLEFINS; COMPLEXES; LIGANDS; KETONES; OXIDES; SERIES; ACIDS;
D O I
10.1016/j.jorganchem.2012.04.002
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The asymmetric hydrogenation of olefins is a tremendously powerful tool used to synthesize chiral molecules. The field was pioneered using rhodium-and ruthenium-based catalysts; however, catalysts based on both of these metals suffer from limitations, such as the need for directing substituents near or even adjacent to the olefin. Iridium-based catalysts do not suffer from this flaw and can thus hydrogenate a wide variety of olefins, including some tetra substituted ones. It is also possible for iridium-based catalysts to hydrogenate hetero-pi bonds such as those found in hetero-aromatic rings. This review summarizes the contributions made to this field by our research group over the past few years. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:3 / 11
页数:9
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