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	Asymmetric aldol reaction organocatalyzed by bifunctional N-prolyl sulfinamides under solvent-free conditions
	Wan, Wen[1]; Gao, Wei[2]; Ma, Guobin[3]; Ma, Lei[4]; Wang, Fan[5]; Wang, Jing[6]; Jiang, Haizhen[7]; Zhu, Shizheng[8]; Hao, Jian[9]
刊名	RSC ADVANCES
	2014
卷号	4页码:26563-26568
ISSN号	2046-2069
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/2276762
专题	上海大学
作者单位	1.[1]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 2.[2]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 3.[3]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 4.[4]State Food & Drug Adm, Ctr Drug Evaluat, Beijing 100038, Peoples R China. 5.[5]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 6.[6]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 7.[7]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 8.[8]Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China. 9.[9]Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China. 10.Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China.
推荐引用方式 GB/T 7714	Wan, Wen[1],Gao, Wei[2],Ma, Guobin[3],et al. Asymmetric aldol reaction organocatalyzed by bifunctional N-prolyl sulfinamides under solvent-free conditions[J]. RSC ADVANCES,2014,4:26563-26568.
APA	Wan, Wen[1].,Gao, Wei[2].,Ma, Guobin[3].,Ma, Lei[4].,Wang, Fan[5].,...&Hao, Jian[9].(2014).Asymmetric aldol reaction organocatalyzed by bifunctional N-prolyl sulfinamides under solvent-free conditions.RSC ADVANCES,4,26563-26568.
MLA	Wan, Wen[1],et al."Asymmetric aldol reaction organocatalyzed by bifunctional N-prolyl sulfinamides under solvent-free conditions".RSC ADVANCES 4(2014):26563-26568.

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