Abstract
The photochemical version of the Boulton–Katritzky reaction has been studied, examining the behaviour of the arylhydrazones of 3-benzoyl-5-X-1,2,4-oxadiazoles. The effect of several modifications of the substrates structure (the E and/or Z structures of arylhydrazones, the possible presence of substituents in the arylhydrazono moiety, and the nature of substituents at C-5 of the 1,2,4-oxadiazole ring) on the course of the photochemical rearrangement has been examined.
| Lingua originale | English |
|---|---|
| pagine (da-a) | 1383-1388 |
| Numero di pagine | 6 |
| Rivista | PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES |
| Volume | 11 |
| Stato di pubblicazione | Published - 2012 |
All Science Journal Classification (ASJC) codes
- Physical and Theoretical Chemistry
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Frenna, V., Marullo, S., D'Auria, M., Viggiani, L., Racioppi, R., & Spinelli, D. (2012). Photochemical isomerization of aryl hydrazones of 1,2,4-oxadiazole derivatives into the corresponding triazoles. PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 11, 1383-1388.