Asymmetric catalysis with chiral primary amine-based organocatalysts

被引:448
作者
Xu, Li-Wen [1 ,2 ]
Luo, Jie [1 ]
Lu, Yixin [1 ,3 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Hangzhou Normal Univ, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 310012, Zhejiang, Peoples R China
[3] Natl Univ Singapore, Inst Life Sci, Med Chem Program, Singapore 117543, Singapore
关键词
DIELS-ALDER REACTION; ENANTIOSELECTIVE MICHAEL ADDITION; DIRECT ALDOL REACTIONS; SELECTIVE MANNICH REACTIONS; QUATERNARY CARBON CENTERS; DIRECT CONJUGATE ADDITION; DIRECT SYN-ALDOL; ALPHA; BETA-UNSATURATED KETONES; TRANSFER HYDROGENATION; ORGANIC CATALYSIS;
D O I
10.1039/b821070e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the past few years, primary amine catalysts derived from natural amino acids, Cinchona alkaloids and other chiral amines have emerged as readily available, highly versatile and extremely powerful catalysts in asymmetric synthesis. They have been demonstrated to be effective catalysts in a wide range of enantioselective organic reactions. In comparison with secondary amine-mediated transformations, the use of primary amine organocatalysts has often been shown to be complementary or superior.
引用
收藏
页码:1807 / 1821
页数:15
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