Chiral Phosphoric Acid Catalyzed Asymmetric Addition of 2-(Vinyloxy)ethanol to Imines and Applications of the Products

被引:6
|
作者
Wu, Xudong [1 ]
Yuan, Xi [1 ]
Yang, Haijun [1 ]
Fu, Hua [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
PHARMACOLOGICAL EVALUATION; REVERSE-TRANSCRIPTASE; BRONSTED ACID; INHIBITORS; HYDROGENATION; AZETIDINES; DIACYLHYDRAZINE; ANTAGONIST; ACTIVATION; ZETIDOLINE;
D O I
10.1021/acs.orglett.9b01970
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Chiral nitrogen-containing molecules such as chiral amines, azetidines, and 2-substituted tetrahydroquinolines are important privileged scaffolds in medicinal chemistry. In this paper, an efficient and highly enantioselective chiral phosphoric acid catalyzed asymmetric addition of 2-(vinyloxy)ethanol to imines has been developed for the first time, providing the corresponding chiral amines containing dioxolane acetals that can transform into useful chiral N-heterocycles including azetidines and 2-substituted tetrahydroquinolines with excellent optical purity.
引用
收藏
页码:5335 / 5340
页数:6
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