中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Organocatalytic asymmetric biomimetic transamination of alpha-keto acetals to chiral alpha-amino acetals

文献类型:期刊论文

作者Pan, Hongjie1; Xie, Ying1; Liu, Mao1; Shi, Yian1,2
刊名RSC ADVANCES
出版日期2014
卷号4期号:5页码:2389-2392
ISSN号2046-2069
DOI10.1039/c3ra42906g
英文摘要This paper describes a chiral base-catalyzed asymmetric biomimetic transamination of alpha-keto acetals. A wide variety of alpha-amino acetals containing various functional groups can be synthesized in 50-85% yield and 82-86% ee.
语种英语
WOS记录号WOS:000329035400042
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/51839]  
专题中国科学院化学研究所
通讯作者Shi, Yian
作者单位1.Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
2.Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
推荐引用方式
GB/T 7714
Pan, Hongjie,Xie, Ying,Liu, Mao,et al. Organocatalytic asymmetric biomimetic transamination of alpha-keto acetals to chiral alpha-amino acetals[J]. RSC ADVANCES,2014,4(5):2389-2392.
APA Pan, Hongjie,Xie, Ying,Liu, Mao,&Shi, Yian.(2014).Organocatalytic asymmetric biomimetic transamination of alpha-keto acetals to chiral alpha-amino acetals.RSC ADVANCES,4(5),2389-2392.
MLA Pan, Hongjie,et al."Organocatalytic asymmetric biomimetic transamination of alpha-keto acetals to chiral alpha-amino acetals".RSC ADVANCES 4.5(2014):2389-2392.

入库方式: OAI收割

来源:化学研究所

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