ICCAS OpenIR
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
Xu, ZH; Jie, YF; Wang, MX; Huang, ZT
2002-03-01
Source PublicationSYNTHESIS-STUTTGART
ISSN0039-7881
Issue4Pages:523-527
AbstractHeterocyclic 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.
KeywordHeterocyclic Ketene Aminals Ethyl 2-(bromomEthyl)Benzoate 1h-imidazo[1 2-b][2]Benzazepin-5-one
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000174601100015
PublisherGEORG THIEME VERLAG KG
Citation statistics
Cited Times:22[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/79106
Collection中国科学院化学研究所
Corresponding AuthorHuang, ZT
AffiliationChinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
Recommended Citation
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.
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