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	Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine
	Cheng Wen-Fu[1]; Chen Ling-Yan[2]; Xu Fang-Fang[3]; Lin Wei-Yu[4]; Ren Xinfeng[5]; Li Ya[6]
刊名	Organic & biomolecular chemistry
	2019
卷号	17页码:885-891
ISSN号	1477-0539
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/2164592
专题	上海大学
作者单位	College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai 201620, China. lingyan.chen@hotmail.com ya.li@sues.edu.cn.
推荐引用方式 GB/T 7714	Cheng Wen-Fu[1],Chen Ling-Yan[2],Xu Fang-Fang[3],et al. Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine[J]. Organic & biomolecular chemistry,2019,17:885-891.
APA	Cheng Wen-Fu[1],Chen Ling-Yan[2],Xu Fang-Fang[3],Lin Wei-Yu[4],Ren Xinfeng[5],&Li Ya[6].(2019).Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine.Organic & biomolecular chemistry,17,885-891.
MLA	Cheng Wen-Fu[1],et al."Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine".Organic & biomolecular chemistry 17(2019):885-891.

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