Organocatalytic Asymmetric [4+2] Cycloaddition Reactions

被引:0
|
作者
Wang Chun [1 ]
Liu Weihua [1 ]
Zhou Xin [1 ]
Li Yuemin [1 ]
Li Yunpeng [1 ]
机构
[1] Agr Univ Hebei, Coll Sci, Hebei Key Lab Bioinorgan Chem, Baoding 071001, Peoples R China
关键词
asymmetric organocatalysis; asymmetric [4+2] cycloaddition reaction; chiral compounds; DIELS-ALDER REACTION; CHIRAL BRONSTED ACID; ALPHA; BETA-UNSATURATED KETONES; ENANTIOSELECTIVE CATALYSIS; ORGANIC CATALYSIS; BRASSARDS DIENE; DIAMINE SALTS; IMIDAZOLIDIN-4-ONE; DESIGN; STRATEGIES;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organocatalytic asymmetric reaction is an increasingly active area in organic synthesis. The asymmetric [4 + 2] cycloaddition (Diels-Alder) reaction is a versatile tool for the synthesis of a large number of important chiral building blocks and intermediates in the total synthesis of natural products. The reported organocatalysts for asymmetric Diels-Alder reaction include imidazolidinone derivatives, chiral Bronsted acids, chiral primary amines, cinchona alkaloids, etc. The applications of various organocatalysts in asymmetric Diels-Alder reaction and the asymmetric induction mechanism are reviewed in this paper.
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页码:1857 / 1868
页数:12
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