中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Total Syntheses of (-)-Huperzine Q and (+)-Lycopladines B and C

文献类型:期刊论文

作者Wu, Jinbao1,2; Hong, Benke1,2; Lei, Xiaoguang1,3,4; Li, Houhua1; Zhang, Jing1,2
刊名ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
出版日期2015-01-12
卷号54期号:3页码:1011-1015
关键词Alkaloids Epoxyamines Metathesis Natural Products Total Synthesis
ISSN号1433-7851
DOI10.1002/anie.201409503
文献子类Article
英文摘要Utilizing a late-stage enamine bromofunctionalization strategy, the twelve-step total synthesis of (-)-huperzine Q was accomplished. Furthermore, the first total syntheses of (+)-lycopladines B and C are described. An unprecedented X-ray crystal structure of an unusual epoxyamine intermediate is also reported, and the synthetic application of this intermediate in natural product synthesis is demonstrated.
WOS关键词LYCOPODIUM ALKALOIDS ; CARBONYL OLEFINATION ; FUNCTIONAL-GROUP ; RECENT PROGRESS ; ENOL ETHERS ; ALKENES ; EPOXYAMINES ; REAGENTS ; FAWCETTIMINE ; METATHESIS
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000348372200053
出版者WILEY-V C H VERLAG GMBH
源URL[http://cas-ir.dicp.ac.cn/handle/321008/167364]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Lei, Xiaoguang
作者单位1.NIBS, Beijing 102206, Peoples R China
2.Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin 300072, Peoples R China
3.Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Bioorgan Chem & Mol Engn, Minist Educ,Dept Chem Biol,Coll Chem & Mol Engn,S, Beijing 100871, Peoples R China
4.Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China
推荐引用方式
GB/T 7714
Wu, Jinbao,Hong, Benke,Lei, Xiaoguang,et al. Total Syntheses of (-)-Huperzine Q and (+)-Lycopladines B and C[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2015,54(3):1011-1015.
APA Wu, Jinbao,Hong, Benke,Lei, Xiaoguang,Li, Houhua,&Zhang, Jing.(2015).Total Syntheses of (-)-Huperzine Q and (+)-Lycopladines B and C.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,54(3),1011-1015.
MLA Wu, Jinbao,et al."Total Syntheses of (-)-Huperzine Q and (+)-Lycopladines B and C".ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 54.3(2015):1011-1015.

入库方式: OAI收割

来源:大连化学物理研究所

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