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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5060
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dc.contributor.authorBasawaraj R
dc.contributor.authorGoled S.N
dc.contributor.authorParmeshwarappa G
dc.contributor.authorSangapure S.S.
dc.date.accessioned2020-06-12T15:06:05Z-
dc.date.available2020-06-12T15:06:05Z-
dc.date.issued2009
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 18 , 4 , p. 325 - 328en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5060-
dc.description.abstractMichael condensation of 2-arylideneacetylbenzofurans 2a-f with ethyl cyanoacetate and malononitrile afforded 4-aryl-6-(benzofuran-2'-yl) nicotinonitrile-2-ones 3a-f and 2- amino-4-aryl-6-(benzofuran-2'-yl)-3- cyanopyridines 4a-f respectively. All the prepared compounds were characterized using spectral and analytical data. Some compounds showed good antimicrobial activity.en_US
dc.titleSynthesis and biological activity of some pyridyl substituted benzofuransen_US
dc.typeArticle
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