中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
SmI_2-promoted imino-Reformatsky reaction for facile synthesis of enantioenriched β-amino acid esters

文献类型:期刊论文

作者Wang Li; Shen Chun; Xu Minghua
刊名Science China. Chemistry
出版日期2011
卷号54期号:1页码:61
关键词β-amino acid ester samarium diiodide N-tert-butanesulfinyl imine Reformatsky reaction β-lactam 3-aminoindan-1one asymmetric synthesis
ISSN号1674-7291
英文摘要A facile and efficient method for the stereoselective synthesis of β-amino acid esters via SmI2-promoted imino-Reformatsky reaction is described. Asymmetric addition of tert-butyl bromoacetate to N-tert-butanesulfinyl aldimines afforded β-amino acid esters in moderate to high yields with excellent diastereoselectivities. The synthetic utilities of the tert-butyl β-amino acid esters were expanded by the preparation of β-lactams and 3-aminoindan-1-ones derivatives
语种英语
源URL[http://119.78.100.183/handle/2S10ELR8/293172]  
专题中国科学院上海药物研究所
作者单位中国科学院上海药物研究所
推荐引用方式
GB/T 7714
Wang Li,Shen Chun,Xu Minghua. SmI_2-promoted imino-Reformatsky reaction for facile synthesis of enantioenriched β-amino acid esters[J]. Science China. Chemistry,2011,54(1):61.
APA Wang Li,Shen Chun,&Xu Minghua.(2011).SmI_2-promoted imino-Reformatsky reaction for facile synthesis of enantioenriched β-amino acid esters.Science China. Chemistry,54(1),61.
MLA Wang Li,et al."SmI_2-promoted imino-Reformatsky reaction for facile synthesis of enantioenriched β-amino acid esters".Science China. Chemistry 54.1(2011):61.

入库方式: OAI收割

来源:上海药物研究所

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