Catalytic Asymmetric Reductive Amination of α-Branched Ketones

被引:120
作者
Wakchaure, Vijay N. [1 ]
Zhou, Jian [1 ]
Hoffmann, Sebastian [1 ]
List, Benjamin [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
关键词
asymmetric catalysis; chiral amines; ketones; organocatalysis; reductive amination; DYNAMIC KINETIC RESOLUTION; BRONSTED ACID CATALYST; TRANSFER HYDROGENATION; SUBSTITUTED SPIROPIPERIDINES; ENANTIOSELECTIVE REDUCTION; ORGANOCATALYTIC REDUCTION; AROMATIC KETIMINES; PHOSPHORIC-ACID; IMINO ESTERS; AMINO-ACIDS;
D O I
10.1002/anie.201001715
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemical equcation Presented Branching out: An organocatalytic reductive amination of -αbranched ketones using dynamic kinetic resolution is reported. The e/s-2-substituted cyclohexyl amines were obtained in high diastereoselectivity and enantioselectivity from the corresponding ketones. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:4612 / 4614
页数:3
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