Enantioselective Nickel-Catalyzed Domino and Tandem Processes

被引：24
作者：
Pellissier, Helene [1 ]
机构：
[1] Aix Marseille Univ, Cent Marseille, CNRS, UMR 7313 13397 iSm2, F-13397 Marseille 20, France
来源：
CURRENT ORGANIC CHEMISTRY | 2016年 / 20卷 / 03期
关键词：
Domino reactions; multicomponent reactions; tandem sequences; one-pot reactions; nickel; asymmetric synthesis; asymmetric catalysis; 1,3-DIPOLAR CYCLOADDITION REACTIONS; ASYMMETRIC MULTICOMPONENT REACTIONS; CYCLIC 1,3-DICARBONYL COMPOUNDS; TRANSITION-METAL CATALYSIS; MICHAEL ADDITION-REACTIONS; IMINO-REFORMATSKY REACTION; CROSS-COUPLING REACTIONS; CHIRAL LEWIS-ACIDS; ORGANIC-SYNTHESIS; ONE-POT;
D O I：
10.2174/1385272819666150909235830
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The goal of this review is to provide a comprehensive overview of the developments in enantioselective two- and multicomponent domino reactions as well as tandem sequences catalyzed by chiral nickel complexes, covering the literature since the beginning of 2004. Related to the lower costs of nickel catalysts in comparison with other transition metals, enantioselective nickel-catalyzed domino and sequential tandem processes have been widely developed in the last decade, allowing a fast and easy approach to complex chiral products in single steps.
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页码：234 / 265
页数：32
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