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
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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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