THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES

The reaction of cyanoacetylhydrazine with co-bromoacetophenone gave the condensation product p-Bromoacetophenone-a-cyanoacetylhydrazone (3). The latter product underwent ready cyclization to give the 1,3,4-oxadiazine derivative 4. The reactivities of either 3 or 4 towards some chemical reagents like...

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Autores principales: MOHAREB,RAFAT M, IBRAHIM,REHAB A, HO,JONATHAN Z
Lenguaje:English
Publicado: Sociedad Chilena de Química 2007
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100005
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spelling oai:scielo:S0717-970720070001000052007-05-07THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVESMOHAREB,RAFAT MIBRAHIM,REHAB AHO,JONATHAN Z Cyanoacetylhydrazine 1,3,4-Oxadiazine Pyridazine Toxicity The reaction of cyanoacetylhydrazine with co-bromoacetophenone gave the condensation product p-Bromoacetophenone-a-cyanoacetylhydrazone (3). The latter product underwent ready cyclization to give the 1,3,4-oxadiazine derivative 4. The reactivities of either 3 or 4 towards some chemical reagents like cyanomethylene reagents, diazonium salts, aromatic aldehydes, phenylisothio-cyanate and elemental sulfur were studied to afford 17 newly producís for which the toxicity towards Fusarium oxysporum f. sp. Lycopersici and Helminthosporium oryzea was measured. Moreover their effect towards mycelial dry mass, sporulation and nucleic acid synthesis of Fusarium oxysporum f. sp. Lycopersici was measuredinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.52 n.1 20072007-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100005en10.4067/S0717-97072007000100005
institution Scielo Chile
collection Scielo Chile
language English
topic Cyanoacetylhydrazine
1,3,4-Oxadiazine
Pyridazine
Toxicity
spellingShingle Cyanoacetylhydrazine
1,3,4-Oxadiazine
Pyridazine
Toxicity
MOHAREB,RAFAT M
IBRAHIM,REHAB A
HO,JONATHAN Z
THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
description The reaction of cyanoacetylhydrazine with co-bromoacetophenone gave the condensation product p-Bromoacetophenone-a-cyanoacetylhydrazone (3). The latter product underwent ready cyclization to give the 1,3,4-oxadiazine derivative 4. The reactivities of either 3 or 4 towards some chemical reagents like cyanomethylene reagents, diazonium salts, aromatic aldehydes, phenylisothio-cyanate and elemental sulfur were studied to afford 17 newly producís for which the toxicity towards Fusarium oxysporum f. sp. Lycopersici and Helminthosporium oryzea was measured. Moreover their effect towards mycelial dry mass, sporulation and nucleic acid synthesis of Fusarium oxysporum f. sp. Lycopersici was measured
author MOHAREB,RAFAT M
IBRAHIM,REHAB A
HO,JONATHAN Z
author_facet MOHAREB,RAFAT M
IBRAHIM,REHAB A
HO,JONATHAN Z
author_sort MOHAREB,RAFAT M
title THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
title_short THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
title_full THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
title_fullStr THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
title_full_unstemmed THE REACTION OF CYANOACETYLHYDRAZINE WITH w-BROMOACETOPHENONE: NOVEL SYNTHESIS OF 1,3,4-OXADIAZINE, PYRIDAZINE AND COUMARIN DERIVATIVES
title_sort reaction of cyanoacetylhydrazine with w-bromoacetophenone: novel synthesis of 1,3,4-oxadiazine, pyridazine and coumarin derivatives
publisher Sociedad Chilena de Química
publishDate 2007
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100005
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