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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5071
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dc.contributor.authorYadav, DB
dc.contributor.authorVenkatesh, KB
dc.contributor.authorSangapure, SS
dc.date.accessioned2020-06-12T15:06:07Z-
dc.date.available2020-06-12T15:06:07Z-
dc.date.issued2009
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 19 , 2 , p. 117 - 120en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5071-
dc.description.abstractClaisen-Schmidt condensation of 2-acetyl benzofuran 1 with aromatic aldehydes in presence of strong alkali gave 3-aryl-1-(2-benzofuryl)-2-propen-1-ones 2a-c. Reaction of 2a-c with guanidine nitrate in ethanol in presence of sodium hydroxide yielded 2-amino6-aryl-4-(benzofuran-2-yl) pyrimidines 3a-c. The reactions of 3a-c with different reagents furnished compounds 4,5,6 and 7. Newly synthesized compounds were evaluated for their antimicrobial and antiinflammatory activities.en_US
dc.publisherCONNECT JOURNALS
dc.titleSYNTHESIS AND BIOLOGICAL EVALUATION OF 3-ARYL-1-(2-BENZOFURYL)-2-PROPEN-1-ONE ANALOGUESen_US
dc.typeArticle
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