Synthesis of 1, 3-diketone and its reaction with different N-nucleophiles (part II)

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Abstract

Treatment of resorcinol with ethyl acetoacetate in presence of conc. sulphuric acid led to formation of 1,3-diketone 3 in several steps, which on reaction with ethylene diamine 4, phenylene diamine 6, hydroxylamine 8, phenyl hydrazine 9 and hydrazine 10 led to formation of 1,4 diazepine 3a, 1, 5-benzodiazepine 3b, isoxazole 3c and pyrazole 3d, 3e derivatives respectively.

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Unny, R., Joshi, P., Dobhal, M. P., & Joshi, Y. C. (2003). Synthesis of 1, 3-diketone and its reaction with different N-nucleophiles (part II). Heterocyclic Communications, 9(2), 171–174. https://doi.org/10.1515/HC.2003.9.2.171

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