Paper
Studies With Enamines: Synthesis and Reactivity of 4-Nitrophenyl-1-piperidinostyrene. Synthesis of Pyridazine, Oxadiazole, 1,2,3-Triazole and 4-Aminopyrazole Derivatives
Published Feb 1, 2007 · Tayseer A. Abdallah, A. M. Salaheldin, N. Radwan
Zeitschrift für Naturforschung B
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Abstract
4-Nitrophenyl-1-piperidinostyrene (4) reacts with an aromatic diazonium salt to afford the arylhydrazonal 6. The latter condenses with active methylene compounds to yield pyridazine derivatives, and with hydroxylamine hydrochloride to produce oxadiazole and 1,2,3-triazole derivatives. Compound 12 was reacted with chloroacetonitrile to afford 4-aminopyrazoles 15.
Study Snapshot
4-Nitrophenyl-1-piperidinostyrene (4) reacts with aromatic diazonium salts to afford arylhydrazonal 6, which condenses with active methylene compounds to yield pyridazine derivatives, oxadiazole, 1,2,3
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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