| نویسندگان | Ramazani A., Zeinalia Nasrabadi F., Ahmadi Y. |
| نشریه | Helvetica Chimica Acta |
| كد DOI/DOR | 10.1002/hlca.201000356 |
| تاریخ انتشار | ۲۰۱۱ |
چکیده مقاله
The 1:1 imine intermediate 7 generated by the addition of a primary amine 2 to chloroacetone (1) is trapped by (isocyanoimino)triphenylphosphorane (4) in the presence of an aromatic carboxylic acid 3 and leads to the formation of the corresponding iminophosphorane intermediate 9 (Schemea 2). The 1,3,4-oxadiazole derivatives 5 are then formed via an intramolecular aza-Wittig reaction of the iminophosphorane intermediate 9. The reactions were completed under neutral conditions at room temperature. The fully substituted 1,3,4-oxadiazole derivatives 5 were produced in high yields (Table). © 2011 Verlag Helvetica Chimica Acta AG, Zürich, Switzerland.
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