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
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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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