6533b825fe1ef96bd1282f7a

RESEARCH PRODUCT

The Boulton-Katritzky Reaction: A Kinetic Study of the Effect of 5-Nitrogen Substituents on the Rearrangement of Some (Z)-phenylhydrazones of 3-Benzoyl-1,2,4-oxadiazoles

V. FrennaA. Palumbo PiccionelloB. CosimelliFranco GhelfiD. Spinelli

subject

hydrazoneKinetics Rearrangement Heterocycles Hydrazones IsomerizationrearrangementkineticSettore CHIM/06 - Chimica OrganicaKinetics / Rearrangement / Heterocycles / Hydrazones / Isomerizationisomerizationheterocycle

description

The kinetics of the ring-into-ring conversion of some new (Z)-phenylhydrazones of 3-benzoyl-1,2,4-oxadiazole containing different nitrogen-substituents at C-5 (3b-d; X = NHMe, NMe2, and NHCOMe) into the relevant triazoles 4b-d have been examined in a wide range of pS+ (0.1-11.9) in 1:1 (v/v) dioxane/water solution. The obtained results have been compared with previous data concerning the (Z)-phenyl-hydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole (3a; X = NH2). All of the studied (Z)-phenylhydrazones rearrange through three different pathways (specific acid-catalysed, uncatalysed and general base-catalysed). The different effects of the substituents on the course of the rearrangement in the three pathways have been examined. © 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

yearjournalcountryeditionlanguage
2014-01-01
10.1002/ejoc.201402569http://hdl.handle.net/10447/101892