中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Sulfa-Michael Addition to alpha-Substituted Vinyl Ketones Catalyzed by Chiral Primary Amine

文献类型:期刊论文

作者Fu, Niankai1; Zhang, Long1,2; Luo, Sanzhong1,2; Cheng, Jin-Pei1,2
刊名ORGANIC LETTERS
出版日期2014-09-05
卷号16期号:17页码:4626-4629
ISSN号1523-7060
DOI10.1021/ol5022178
英文摘要The first effective example of asymmetric conjugate addition-protonation reactions of thiols to alpha-substituted vinyl ketones by chiral primary amine catalysis is reported. A simple chiral primary tertiary diamine catalyst derived from L-phenylalanine was found to promote the sulfa-Michael addition-protonation reactions with good to excellent enantioselectivity.
语种英语
WOS记录号WOS:000341344600071
出版者AMER CHEMICAL SOC
源URL[http://ir.iccas.ac.cn/handle/121111/51983]  
专题中国科学院化学研究所
通讯作者Luo, Sanzhong
作者单位1.Chinese Acad Sci, Inst Chem, BNLMS, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
2.Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
推荐引用方式
GB/T 7714
Fu, Niankai,Zhang, Long,Luo, Sanzhong,et al. Asymmetric Sulfa-Michael Addition to alpha-Substituted Vinyl Ketones Catalyzed by Chiral Primary Amine[J]. ORGANIC LETTERS,2014,16(17):4626-4629.
APA Fu, Niankai,Zhang, Long,Luo, Sanzhong,&Cheng, Jin-Pei.(2014).Asymmetric Sulfa-Michael Addition to alpha-Substituted Vinyl Ketones Catalyzed by Chiral Primary Amine.ORGANIC LETTERS,16(17),4626-4629.
MLA Fu, Niankai,et al."Asymmetric Sulfa-Michael Addition to alpha-Substituted Vinyl Ketones Catalyzed by Chiral Primary Amine".ORGANIC LETTERS 16.17(2014):4626-4629.

入库方式: OAI收割

来源:化学研究所

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