Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21714
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dc.contributor.authorKamel, Mona M-
dc.contributor.authorHussein, Manal M M-
dc.date.accessioned2013-10-09T05:27:10Z-
dc.date.available2013-10-09T05:27:10Z-
dc.date.issued2003-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21714-
dc.description2136-2141en_US
dc.description.abstractA variety of 2-alkoxy-4,6-diaryl-3-pyridinecarbonitriles 2 have been prepared via either the reaction of 1,3-diaryl-2-propen-1-ones 1 with malononitrile or the reaction of ylidenemalononitriles 6 with the proper aryl methyl ketone 7 in the appropriate alcohol in the presence of sodium. On the other hand, conducting the reaction in refluxing ethanol in the presence of ammonium acetate affords, the corresponding 2-amino-3-pyridinecarbonitriles 8. The antimicrobial properties against Gram-positive, Gram-negative, acid-fast bacteria and yeast have been screened. The prepared propenones 1a-d show considerable activity against the tested yeast as well as most of the Gram-positive and Gram-negative bacteria. A few derivatives of the prepared pyridines 2c,f,h ; 8b exhibit mild antimicrobial activity.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(09) [September 2003]en_US
dc.titleSynthetic approaches towards 3-pyridinecarbonitrile derivatives and their antimicrobial propertiesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(09) [September 2003]

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