Arylamine-Catalyzed Enamine Formation: Cooperative Catalysis with Arylamines and Acids

被引:79
作者
Deng, Yongming [1 ]
Liu, Lu [1 ]
Sarkisian, Ryan G. [1 ]
Wheeler, Kraig [3 ]
Wang, Hong [1 ]
Xu, Zhenghu [2 ]
机构
[1] Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[3] Eastern Illinois Univ, Dept Chem, Charleston, IL 61920 USA
基金
美国国家科学基金会;
关键词
aza-DielsAlder reactions; cooperative catalysis; enamines; Lewis acids; multicomponent reactions; DIELS-ALDER REACTION; CHIRAL COUNTERION STRATEGY; ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC CATALYSIS; ALLYLIC ALKYLATION; TRANSITION-METAL; ORGANOCATALYSIS; ALDEHYDES; CARBOCYCLIZATION; COMBINATION;
D O I
10.1002/anie.201209268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Powerful combination: Arylamines and metal Lewis acids are used as catalysts in the highly chemo- and enantioselective three-component inverse-electron-demand aza-Diels-Alder reaction of cyclic ketones with enones. The enantioselectivity is introduced by a simple chiral anion (see scheme). Arylamines can also serve as effective enamine catalysts in combination with either a metal Lewis acid or a Brønsted acid. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:3663 / 3667
页数:5
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