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  4. Indian Journal of Chemistry -Section B (IJC-B)
  5. IJC-B Vol.48B [2009]
  6. IJC-B Vol.48B(10) [October 2009]
Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6112
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dc.contributor.authorBrahmeshwari, G-
dc.date.accessioned2009-10-08T04:17:44Z-
dc.date.available2009-10-08T04:17:44Z-
dc.date.issued2009-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print-
dc.identifier.urihttp://hdl.handle.net/123456789/6112-
dc.description1457-1461en_US
dc.description.abstract Condensation of Embelin 1 with different aromatic acid hydra­zides 2 in glacial acetic acid to give N1-5-hydroxy-6-unde­cyl-p-benzoaquinone-2-yl)-benzohydrides 3. Reductive cycli­za­tion of the product 3 with simultaneous acetylation in situ resulted in the formation of the compound 4 1-N-acetyl-6,7-diacetyl-3-aryl-5-undecyl-4,1,2-benzoxadiazine. In the final step the compound 4 is deacetylated to give the title products 5. The structures of the newly prepared compounds have been confirmed from analytical and spectral data. Some of the compounds exhibited antibacterial and antifungal activity. en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(10) [October 2009]en_US
dc.subjectEmbelinen_US
dc.subjectacid hydrazidesen_US
dc.subjectacetylationen_US
dc.subjectcyclization reactionen_US
dc.subjectantibacterialen_US
dc.subjectantifungalen_US
dc.titleSynthesis of 6,7-dihydroxy-3-aryl-5-undecyl-4,1,2-benzoxadiazinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(10) [October 2009]

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