中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chiral Phosphoric Acid Catalyzed Highly Enantioselective Friedel-Crafts Alkylation Reaction of C3-Substituted Indoles to beta,gamma-Unsaturated alpha-Ketimino Esters

文献类型:期刊论文

作者Zhao, Jun-Ling; Hu, Wen-Hui; Bi, Bo; Lou, Qin-Xin; Ding, Yu-Yang; Chen, Sheng-Wei; Zhang, Sha-Sha
刊名ORGANIC LETTERS
出版日期2015
卷号17期号:3页码:540-543
ISSN号1523-7060
学科主题Chemistry
语种英语
源URL[http://ir.foo.ac.cn/handle/2SETSVCV/35]  
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
Zhao, Jun-Ling,Hu, Wen-Hui,Bi, Bo,et al. Chiral Phosphoric Acid Catalyzed Highly Enantioselective Friedel-Crafts Alkylation Reaction of C3-Substituted Indoles to beta,gamma-Unsaturated alpha-Ketimino Esters[J]. ORGANIC LETTERS,2015,17(3):540-543.
APA Zhao, Jun-Ling.,Hu, Wen-Hui.,Bi, Bo.,Lou, Qin-Xin.,Ding, Yu-Yang.,...&Zhang, Sha-Sha.(2015).Chiral Phosphoric Acid Catalyzed Highly Enantioselective Friedel-Crafts Alkylation Reaction of C3-Substituted Indoles to beta,gamma-Unsaturated alpha-Ketimino Esters.ORGANIC LETTERS,17(3),540-543.
MLA Zhao, Jun-Ling,et al."Chiral Phosphoric Acid Catalyzed Highly Enantioselective Friedel-Crafts Alkylation Reaction of C3-Substituted Indoles to beta,gamma-Unsaturated alpha-Ketimino Esters".ORGANIC LETTERS 17.3(2015):540-543.

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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