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学科主题: 有机化学
题名: ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION
其他题名: 手性布朗斯特酸催化的分子内氮杂Michael反应不对称合成2-芳基-2,3-二氢-4-喹啉酮衍生物
作者: Feng Z(冯桢) ; Xu QL(许庆龙) ; Dai LX(戴立信) ; You SL(游书力)
通讯作者: 游书力
刊名: Heterocycles
发表日期: 2010
卷: 80, 期:2, 页:765-771
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所
英文摘要: Asymmetric intramolecular aza-Michael addition of activated alpha,beta-unsaturated ketones catalyzed by chiral N-triflyl phosphoramide was realized. Enantioenriched 2-aryl-2,3-dihydroquinolin-4-ones can be obtained in excellent yields (77-98%) with up to 82% ee.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000276939500004
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/16007
Appears in Collections:金属有机化学国家重点实验室_期刊论文

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Recommended Citation:
Feng Z,Xu QL,Dai LX,et al. ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION[J]. Heterocycles,2010,80(2):765-771.
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