Enantioselective transfer hydrogenation, a key step for the synthesis of 3-aminotetrahydroquinolines

被引：10
|
作者：
Aillerie, Alexandre [1 ]
de Talence, Vincent Lemau [1 ]
Dumont, Clement [1 ]
Pellegrini, Sylvain [1 ]
Capet, Frederic [1 ]
Bousquet, Till [1 ]
Pelinski, Lydie [1 ]
机构：
[1] Univ Artois, Univ Lille, CNRS, UMR 8181,Cent Lille,ENSCL,UCCS, F-59000 Lille, France
来源：
NEW JOURNAL OF CHEMISTRY | 2016年 / 40卷 / 11期
关键词：
ASYMMETRIC TRANSFER HYDROGENATION; ORGANOCATALYTIC TRANSFER HYDROGENATION; CYANOBACTERIUM ANABAENA-CYLINDRICA; CHIRAL PHOSPHORIC-ACIDS; BRONSTED ACID; QUINOLINES; ANACHELIN; CYCLIZATION; REDUCTION; TETRAHYDROQUINOLINES;
D O I：
10.1039/c6nj02249a
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
An enantioselective transfer hydrogenation has been successfully achieved to furnish 3-aminotetrahydroquinolines. The reaction was conducted in the presence of Hantzsch dihydropyridine and a catalytic amount of chiral phosphoric acid under mild conditions.
引用
收藏
页码：9034 / 9037
页数：4
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