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Bi, Bo ; Lou, Qin-Xin ; Ding, Yu-Yang ; Chen, Sheng-Wei ; Zhang, Sha-Sha ; Hu, Wen-Hui ; Zhao, Jun-Ling
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
公开日期2016-12-16
源URL[http://ir.gibh.ac.cn/handle/344009/587]  
专题广州生物医药与健康研究院_华南干细胞与再生医学研究所_华南干细胞与再生医学研究所_期刊论文
推荐引用方式
GB/T 7714
Bi, Bo,Lou, Qin-Xin,Ding, Yu-Yang,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 Bi, Bo.,Lou, Qin-Xin.,Ding, Yu-Yang.,Chen, Sheng-Wei.,Zhang, Sha-Sha.,...&Zhao, Jun-Ling.(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 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".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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