ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION

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	ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION
	Feng Z(冯桢) ; Xu QL(许庆龙) ; Dai LX(戴立信) ; You SL(游书力)
刊名	Heterocycles
	2010
卷号	80 期号:2 页码:765-771
ISSN号	0385-5414
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
通讯作者	游书力
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.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.3987/COM-09-S(S)66
语种	英语
WOS记录号	WOS:000276939500004
公开日期	2013-02-19
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/16007]
专题	上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式 GB/T 7714	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.
APA	冯桢,许庆龙,戴立信,&游书力.(2010).ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION.Heterocycles,80(2),765-771.
MLA	冯桢,et al."ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION".Heterocycles 80.2(2010):765-771.