Chiral Phosphoric Acid Catalyzed Kinetic Resolution of 2-Amido Benzyl Alcohols: Asymmetric Synthesis of 4H-3,1-Benzoxazines

被引:53
作者
Rajkumar, Subramani [1 ]
Tang, Mengyao [1 ,2 ]
Yang, Xiaoyu [1 ]
机构
[1] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
alcohols; heterocycles; kinetic resolution; organocatalysis; reaction mechanisms; BRONSTED ACID; ENANTIOSELECTIVE SYNTHESIS; TERTIARY ALCOHOLS; HYDROXY ESTERS; POTENT; CHLOROCYCLIZATION; CYCLOADDITION; CONSTRUCTION; INHIBITORS; ALKYLATION;
D O I
10.1002/anie.201913896
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient method for the asymmetric synthesis of 4H-3,1-benzoxazines was developed by kinetic resolution of 2-amido benzyl alcohols using chiral phosphoric acid catalyzed intramolecular cyclizations. A broad range of benzyl alcohols (both secondary and tertiary alcohols) were kinetically resolved with high selectivities, with an s factor of up to 94. Mechanistic studies were performed to elucidate the mechanism of these reactions, wherein the amide moieties reacted as the electrophiles. Gram-scale reaction and facile transformations of the chiral products demonstrate the potential of this method in asymmetric synthesis of biologically active chiral heterocycles.
引用
收藏
页码:2333 / 2337
页数:5
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