中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Copper-Catalyzed Enantioselective Intramolecular Aryl C-N Coupling: Synthesis of Enantioenriched 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an Asymmetric Desymmetrization Strategy

文献类型:期刊论文

作者Huang, Yusha; Cai, Qian; He, Nian; Huo, Yanping; Liu, Jianguang; Zhang, Shasha
刊名ORGANIC LETTERS
出版日期2015
卷号17期号:2页码:374-377
ISSN号1523-7060
学科主题Chemistry
语种英语
源URL[http://ir.foo.ac.cn/handle/2SETSVCV/32]  
专题中国科学院广州生物医药与健康研究院
推荐引用方式
GB/T 7714
Huang, Yusha,Cai, Qian,He, Nian,et al. Copper-Catalyzed Enantioselective Intramolecular Aryl C-N Coupling: Synthesis of Enantioenriched 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an Asymmetric Desymmetrization Strategy[J]. ORGANIC LETTERS,2015,17(2):374-377.
APA Huang, Yusha,Cai, Qian,He, Nian,Huo, Yanping,Liu, Jianguang,&Zhang, Shasha.(2015).Copper-Catalyzed Enantioselective Intramolecular Aryl C-N Coupling: Synthesis of Enantioenriched 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an Asymmetric Desymmetrization Strategy.ORGANIC LETTERS,17(2),374-377.
MLA Huang, Yusha,et al."Copper-Catalyzed Enantioselective Intramolecular Aryl C-N Coupling: Synthesis of Enantioenriched 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an Asymmetric Desymmetrization Strategy".ORGANIC LETTERS 17.2(2015):374-377.

入库方式: OAI收割

来源:广州生物医药与健康研究院

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