Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16325
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dc.contributor.authorDoshi, Rajeev-
dc.contributor.authorKagthara, Preeti-
dc.contributor.authorParekh, Hansa-
dc.date.accessioned2013-03-09T11:19:02Z-
dc.date.available2013-03-09T11:19:02Z-
dc.date.issued1999-03-
dc.identifier.urihttp://hdl.handle.net/123456789/16325-
dc.description348-352en_US
dc.description.abstractSubstituted chalcones 2a-m prepared by the treatment of 5-benzoyl-benzimidazol-2-yl-o-benzoyl(4' –aminoaceto-phenone) 1 with araldehydes, on cyclisation with hydroxylamine  hydrochloride in ethanol furnish isoxazoles 3a-m. The same chalcones on condensation with malononitrile yield cyanopyridines 4a-m. The structure of the compounds synthesised have been assigned on the basis of elemental analyses, IR and NMR spectral studies. Most of the compounds exhibit significant activity against Mycobacterium tuberculosis H37 Rv and MIC value is reported. Compounds 2c,3c and 4d have been selected by Merck Incorporation USA for further pharmacological screening.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.38B(03) [March 1999]en_US
dc.titleSynthesis and biological evaluation of some novel isoxazoles and cyanopyridines, a new class of potential anti-tubercular agentsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(03) [March 1999]

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