Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6630
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dc.contributor.authorMogilaiah, K-
dc.contributor.authorVidya, K-
dc.date.accessioned2009-11-18T07:43:10Z-
dc.date.available2009-11-18T07:43:10Z-
dc.date.issued2006-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6630-
dc.description1905-1908en_US
dc.description.abstractCondensation of (2-oxo-3-phenyl-2H-[1,8]naphthyridin-1-yl)-acetic acid hydrazide 2 with different acetophenones yields the corresponding acetophenone (2-oxo-3-phenyl-2H-[1,8]naphthyridin-1-yl)methylcarbonyl hydrazones 3, which on treatment with acetic anhydride affords the respective 1-(4-acetyl-5-aryl-5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-3-phenyl-1H-[1,8]naphthyridin-2-ones 4. The structures of the compounds 3 and 4 have been confirmed on the basis of analytical and spectral data. The compounds 4 have been screened for their antibacterial activity.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.8 C07Den_US
dc.sourceIJC-B Vol.45B(08) [August 2006]en_US
dc.subject1,8-Naphthyridinyl acetic acid hydrazideen_US
dc.subjectacetophenonesen_US
dc.subjectcondensationen_US
dc.subject1,8-naphthyridinyl methylcarbonyl hydrazones acetic anhydrideen_US
dc.subjectcyclizationen_US
dc.subject1,3,4-oxadiazolyl-1, 8-naphthyridinesen_US
dc.titleSynthesis and antibacterial activity of 1,3,4-oxadiazolyl-1,8-naphthyridinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(08) [August 2006]

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