Carbohydrate-based organocatalysts in direct asymmetric aqueous aldol reaction

被引:6
|
作者
Mondal, Mohabul A. [1 ]
Mandal, Debashis [1 ]
机构
[1] Univ Gour Banga, Dept Chem, Malda 732103, W Bengal, India
关键词
Aqueous aldol reaction; Asymmetric aldol reaction; Carbohydrates; Organocatalysis; DIELS-ALDER REACTION; HIGHLY EFFICIENT; AROMATIC-ALDEHYDES; D-GLUCOSAMINE; WATER; KETONES; PROLINAMIDE; MEDIA; CHEMISTRY; CATALYSTS;
D O I
10.1080/07328303.2016.1206114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aldol reaction involving chiral amines as organocatalysts through enamine formation, like class-I aldolases, is one of the thriving areas of general interest and widely applicable asymmetric reactions. There are many natural and synthetic chiral templates known to work as efficient organocatalysts, but using carbohydrate templates for chiral induction in asymmetric aldol reactions is a relatively new area developed in the recent years. This review focuses on carbohydrates alone or their conjugates with previously known chiral moieties as organocatalysts for asymmetric aldol reactions.
引用
收藏
页码:181 / 200
页数:20
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