Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9227
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dc.contributor.authorSuresh, T-
dc.contributor.authorDhanabal, T-
dc.contributor.authorKumar, R Nandha-
dc.contributor.authorMohan, P S-
dc.date.accessioned2010-06-01T04:55:36Z-
dc.date.available2010-06-01T04:55:36Z-
dc.date.issued2005-11-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9227-
dc.description2375-2379en_US
dc.description.abstractAn easy two-step synthesis of 1,6-naphthyridines (4a-c, 7a-c, 10a-c, 14a-c) has been arrived from 3-formylquinolin-2(1H)-ones 1a-c and respective arylamines (2, 5, 8, 12) which underwent condensation and aromatized by dehydration with the help of PPA. All the synthesized compounds have been biologically screened for their antibacterial and antifungal activities.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D // A 61 P 31/04, 31/10en_US
dc.sourceIJC-B Vol.44B(11) [November 2005]en_US
dc.subjectBenzoen_US
dc.subjectpyrido-1en_US
dc.subject6-naphthyridinesen_US
dc.subjectcondensationen_US
dc.subjectdehydrationen_US
dc.subjectarylaminesen_US
dc.subjectantibacterial activityen_US
dc.subjectantifungal activityen_US
dc.titleSynthesis, characterization and antimicrobial activities of fused 1,6-naphthyridinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(11) [November 2005]

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