| نویسندگان | Ramazani A., Shajari N., Mahyari A., Ahmadi Y. |
| نشریه | Molecular Diversity |
| كد DOI/DOR | 10.1007/s11030-010-9275-0 |
| تاریخ انتشار | ۲۰۱۱ |
چکیده مقاله
The 1:1 imine intermediate generated by the addition of benzyl amine to cyclobutanone is trapped by (N-isocyanimino)triphenylphosphorane in the presence of an aromatic carboxylic acid leads to the formation of the corresponding iminophosphorane intermediate. Disubstituted 1,3,4-oxadiazole derivatives are formed via intramolecular aza-Wittig reaction of the iminophosphorane intermediate. The reactions were completed in neutral conditions at room temperature. The disubstituted 1,3,4-oxadiazole derivatives, were produced in excellent yields. © Springer Science+Business Media B.V. 2010.
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