Catalytic Asymmetric Construction of Chiral Hydropyridazines via Conjugate Addition of N-Monosubstituted Hydrazones to Enones

被引:46
|
作者
Wu, Wenbin [1 ]
Yuan, Xiaoqian [1 ]
Hu, Juan [1 ]
Wu, Xinxin [1 ]
Wei, Yuan [1 ]
Liu, Zunwu [1 ]
Lu, Junzhu [1 ]
Ye, Jinxing [1 ]
机构
[1] E China Univ Sci & Technol, Sch Pharm, Minist Educ, Engn Res Ctr Pharmaceut Proc Chem, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
FORMALDEHYDE N; N-DIALKYLHYDRAZONES; ENANTIOSELECTIVE SYNTHESIS; ALPHA; BETA-UNSATURATED KETONES; MICHAEL REACTIONS; SAMP-HYDRAZONE; ACID; UMPOLUNG; ANION; REACTIVITY; PYRAZOLINE;
D O I
10.1021/ol4020865
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The first example of a highly enantioselective and scalable formal diaza-ene reaction between N-monosubstituted hydrazones and enones catalyzed by a simple chiral primary-second diamine salt has been developed. The catalytic process provides a highly practical and stereoselective synthetic method for chiral hydropyridazines.
引用
收藏
页码:4524 / 4527
页数:4
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