Recent advances in catalytic enantioselective multicomponent reactions

被引:62
|
作者
Nunes, Paulo Sergio Goncalves [1 ]
Vidal, Herika Danielle Almeida [1 ]
Correa, Arlene G. [1 ]
机构
[1] Univ Fed Sao Carlos, Ctr Excellence Res Sustainable Chem, Dept Chem, Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ASYMMETRIC-SYNTHESIS; REACTIONS AMCRS; BRONSTED ACID; UGI REACTION; CONSTRUCTION; CASCADE; ACCESS;
D O I
10.1039/d0ob01631d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Multicomponent reactions (MCRs) undoubtedly correspond to one of the synthetic strategies that best fit the new demands of chemistry for presenting high atom economy and enabling molecular diversity. However, many challenges still exist when products possessing stereogenic centres are formed. The field of asymmetric catalytic reactions has achieved significant progress in recent decades; new applications for chiral ligands and catalysts have been demonstrated and new catalysts have been specifically designed for challenging chemical conversions. In this sense, highly efficient approaches for classic multicomponent reactions such as the Ugi reaction and a number of new asymmetric MCRs have been described. In this review we discuss the recent developments that enable catalytic enantioselective MCRs including the proposed mechanistic pathways.
引用
收藏
页码:7751 / 7773
页数:23
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