阿托品
对映选择合成
分子内力
胺化
化学
轴手性
催化作用
环己烷
立体化学
组合化学
有机化学
作者
Xiaozhong Fan,Xue Zhang,Chunyu Li,Zhenhua Gu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-01-31
卷期号:9 (3): 2286-2291
被引量:78
标识
DOI:10.1021/acscatal.8b04789
摘要
Catalytically asymmetric synthesis of atropisomeric compounds is an important research area in organic synthesis. However, in comparison with C–C atropisomers, the atropisomers caused by the restricted rotation of C–N single bonds have been given less attention because of the limited methods for accessing these compounds. Herein we report a Cu-catalyzed enantioselective intramolecular Ullmann-type amination reaction for the synthesis of C–N atropisomers. The C–N axial chirality was induced highly efficiently by the intramolecular adjacent C–N cross-coupling. The readily prepared N,N′-(cyclohexane-1,2-diyl)dipicolinamides showed high efficacy and stereoinduction (up to 99% ee).
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