Synthesis of novel functionally substituted pyridazines and oxazines |
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Authors: | M. Hammouda Z. M. Abou Zeid M. A. Metwally |
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Affiliation: | (1) Department of Chemistry, Faculty of Science, University of Mansoura, Mansoura, Egypt |
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Abstract: | Acetone 1,3-di(phenylhydrazone) reacts with arylidenemalononitriles in the presence of piperidine to give the coressponding 3,3′-carbonylbispyridazine derivatives. Under the same reaction conditions dioxime reacts with arylidenemalononitriles to give the corresponding 3,3′-carbonylbis-1,2-oxazines. Dioxime reacts with primary aromatic amines and formalin in a molar ratio of 1:1:2 to give 1-arylidene-3,5-dihydroxyimino-piperidine-4-ones. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1223–1229, August, 2008. |
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Keywords: | acetone 1,3-dioxime,acetone 1,3-diphenylhydrazone,1,2-dioximes pyridazines |
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