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Unprecedented carbon-carbon bond cleavage in nucleophilic aziridine ring opening reaction, efficient ring transformation of aziridines to imidazolidin-4-ones
Wang, Jin-Yuan; Hu, Yuan; Wang, De-Xian; Pan, Jie; Huang, Zhi-Tang; Wang, Mei-Xiang
刊名CHEMICAL COMMUNICATIONS
2009
期号4页码:422-424
ISSN号1359-7345
DOI10.1039/b816007d
英文摘要N-Styryl-3-aryl-1-methylaziridine-2-carboxamides, which were readily obtained from the cross coupling reaction between 3-aryl-1-methylaziridine-2-carboxamides and 1-aryl-2-bromoethenes catalyzed by CuI/N,N-dimethylglycine in the presence of Cs(2)CO(3), underwent a base-mediated intramolecular nucleophilic aziridine ring opening reaction effectively via the carbon carbon bond cleavage of aziridine to afford the ring expanded imidazolidin-4-one products in good yields.
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000262398500010
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/68541]  
专题中国科学院化学研究所
通讯作者Wang, Mei-Xiang
作者单位Chinese Acad Sci, Inst Chem, Biol Chem Lab, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Wang, Jin-Yuan,Hu, Yuan,Wang, De-Xian,et al. Unprecedented carbon-carbon bond cleavage in nucleophilic aziridine ring opening reaction, efficient ring transformation of aziridines to imidazolidin-4-ones[J]. CHEMICAL COMMUNICATIONS,2009(4):422-424.
APA Wang, Jin-Yuan,Hu, Yuan,Wang, De-Xian,Pan, Jie,Huang, Zhi-Tang,&Wang, Mei-Xiang.(2009).Unprecedented carbon-carbon bond cleavage in nucleophilic aziridine ring opening reaction, efficient ring transformation of aziridines to imidazolidin-4-ones.CHEMICAL COMMUNICATIONS(4),422-424.
MLA Wang, Jin-Yuan,et al."Unprecedented carbon-carbon bond cleavage in nucleophilic aziridine ring opening reaction, efficient ring transformation of aziridines to imidazolidin-4-ones".CHEMICAL COMMUNICATIONS .4(2009):422-424.
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