Journal of Heterocyclic Chemistry · 1983 · 18 citations · 5 references
Natural SciencesChemistryOrganic ChemistryStructure-activity RelationshipsSynthetic Medicinal ChemistryOxidation AnalysisOxidation ReactionsThermal DecompositionThermal Decomposition Reactions
Abstract Oxidation of the title bis‐aroylhydrazones 2 with lead tetraacetate gives l‐aroyl‐5‐aroylazo‐3, 4, 4, 5‐tetramethyl‐2‐pyrazolines 6 in good yields. The aroylazopyrazolines 6 decompose by refluxing in chloroform or ethanol solution to l‐aroyl‐5‐hydroxy‐3, 4, 4, 5‐tetramethyl‐2‐pyrazolines 3 , l‐aroyl‐5‐methylene‐3, 4, 4‐trimethyl‐2‐pyrazoles 10 and 1‐aroyl‐3, 4, 4, 5‐tetramethyl‐2‐pyrazolines 11 . The spectral data of the prepared compounds, as well as the reaction mechanisms are discussed.
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H. Bauer, A. J. Boulton, W. Fedeli et al. · Journal of the Chemical Society Perkin Transactions 2 · 1972 · 37 citations
Masao Yokote · Journal of Synthetic Organic Chemistry Japan · 1956 · 32 citations · Full text
Alex G. Harrison, R. Krishna Mohan Rao Kallury · Organic Mass Spectrometry · 1980 · 17 citations
J. G. Schantl · Zeitschrift für Naturforschung B · 1977 · 11 citations · Full text