Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide

被引:34
作者
Li, Jun-Hua [1 ]
Du, Da-Ming [1 ]
机构
[1] Beijing Inst Technol, Sch Chem Engn & Environm, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
ONE-POT SYNTHESIS; HYDROGEN-BONDING ORGANOCATALYSTS; ASYMMETRIC MICHAEL ADDITION; CINCHONA-BASED SQUARAMIDE; BRONSTED ACID; MICHAEL/MICHAEL ADDITION; 1,3-DICARBONYL COMPOUNDS; 2H-CHROMENE DERIVATIVES; VERSATILE CATALYST; HIGHLY EFFICIENT;
D O I
10.1039/c4ob02653e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient chiral squaramide-catalysed enantioselective Michael addition of pyrazolin-5-ones to 3-nitro-2H-chromenes for the synthesis of chiral heterocyclic systems containing both chroman and pyrazolone derivatives has been developed. This reaction afforded the desired products in high to excellent yields (up to 98%) with high enantioselectivities (up to 96%) and excellent diastereoselectivities (up to 99 : 1) under very low catalyst loading (0.2 mol%). This catalytic asymmetric reaction provides an efficient route toward the synthesis of chiral heterocyclic systems containing both chroman and pyrazolone derivatives, which possess potential pharmaceutical activities.
引用
收藏
页码:5636 / 5645
页数:10
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