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
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出版日期 | 2014 |
卷号 | 4期号:5页码:2389-2392 |
ISSN号 | 2046-2069 |
DOI | 10.1039/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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