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Mononuclear heterocyclic rearrangement. Note I. Kinetic study of the rearrangement of the phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole into 2,5-diphenyl-4-benzoylamino-1,2,3-triazole

✍ Scribed by Domenico Spinelli; Anlonino Corrao; Vincenzo Frenna; NicolÒ Vivona; Michele Ruccia; Giuseppe Cusmano

Book ID: 112123715
Publisher: Journal of Heterocyclic Chemistry
Year: 1976
Tongue: English
Weight: 202 KB
Volume: 13
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570130229

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Nonionic Triton X-100 micelles solubilize the otherwise waterinsoluble (Z)-phenylhydrazones of some 5-substituted 3-benzoyl-1,2,4-oxadiazoles to an extent suitable for studying the occurrence of a general-base-catalyzed rearrangement in the presence of borate buffers (pH 9.6). The kinetic data, obta