中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
The regiospecific c-benzylation of heterocyclic ketene aminals with ethyl 2-(bromomethyl)benzoate: A simple route to 1H-1midazo[1,2-b][2]benzazepin-5-one derivatives

文献类型:期刊论文

作者Xu, ZH; Jie, YF; Wang, MX; Huang, ZT
刊名SYNTHESIS-STUTTGART
出版日期2002-03-01
期号4页码:523-527
关键词Heterocyclic Ketene Aminals Ethyl 2-(bromomEthyl)Benzoate 1h-imidazo[1 2-b][2]Benzazepin-5-one
ISSN号0039-7881
英文摘要Heterocyclic ketene aminals reacted with ethyl 2-(bromomethyl)benzoate in refluxing acetonitrile to afford the C-benzylated products that underwent intramolecular cyclocondensation reaction to produce epsilon-lactam fused heterocyclic compounds. The heterocyclic ring size effect on the reaction was discussed.
语种英语
WOS记录号WOS:000174601100015
出版者GEORG THIEME VERLAG KG
源URL[http://ir.iccas.ac.cn/handle/121111/79105]  
专题中国科学院化学研究所
通讯作者Huang, ZT
作者单位Chinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Xu, ZH,Jie, YF,Wang, MX,et al. The regiospecific c-benzylation of heterocyclic ketene aminals with ethyl 2-(bromomethyl)benzoate: A simple route to 1H-1midazo[1,2-b][2]benzazepin-5-one derivatives[J]. SYNTHESIS-STUTTGART,2002(4):523-527.
APA Xu, ZH,Jie, YF,Wang, MX,&Huang, ZT.(2002).The regiospecific c-benzylation of heterocyclic ketene aminals with ethyl 2-(bromomethyl)benzoate: A simple route to 1H-1midazo[1,2-b][2]benzazepin-5-one derivatives.SYNTHESIS-STUTTGART(4),523-527.
MLA Xu, ZH,et al."The regiospecific c-benzylation of heterocyclic ketene aminals with ethyl 2-(bromomethyl)benzoate: A simple route to 1H-1midazo[1,2-b][2]benzazepin-5-one derivatives".SYNTHESIS-STUTTGART .4(2002):523-527.

入库方式: OAI收割

来源:化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。