Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21557
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dc.contributor.authorMogilaiah, K-
dc.contributor.authorKankaiah, G-
dc.date.accessioned2013-10-04T12:15:52Z-
dc.date.available2013-10-04T12:15:52Z-
dc.date.issued2003-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21557-
dc.description658-660en_US
dc.description.abstractCondensation of 2-phenyl-1,8-naphthyridine-3-carboxylic acid hydrazide 1 with β-aroylpropionic acids 2 in ethanol affords the corresponding N-(2-phenyl-1,8-naphthyridine-3-carbonyl)-β-aroylpropionic acid hydrazones 3, which on treatment with gl. acetic acid undergo facile cyclization to yield 6-aryl-2-(2-phenyl 1,8-naphthyridine 3-carbonyl)-4,5-di hydro-pyridazin-3(2H)-ones 4. The compounds 4 have been tested for their antibacterial activity. The structures of the products have been delineated by elemental analyses and spectral studies.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(03) [March 2003]en_US
dc.titleSynthesis of 6-aryl-2-(2-phenyl-1,8-naphthyridine-3-carbonyl)-4,5-dihydropyridazin- 3(2H)-ones en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(03) [March 2003]

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