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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5821
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dc.contributor.authorBasawaraj R
dc.contributor.authorYadav B
dc.contributor.authorSangapure S.S.
dc.date.accessioned2020-06-12T15:08:58Z-
dc.date.available2020-06-12T15:08:58Z-
dc.date.issued2001
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 11 , 1 , p. 31 - 34en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5821-
dc.description.abstractThe condensation of 5-chloro-3-methyl-2-acetyl benzofuran (1) with aromatic aldehydes in presence of alkali gave 2-cinnamoyl-5-chloro-3-methyl benzofurans (2-6) which reacted with hydrazine hydrate to furnish 5-aryl-3-(5-chloro-3-methyl benzofuran-2-yl)-1H-pyrazolines (7-11). Acetylation and benzoylation of 7-11 offered 1-acetyl and 1-benzoyl pyrazolines (12-21). The invitro antimicrobial activity of the compounds is described.en_US
dc.titleSynthesis of some 1H-pyrazolines bearing benzofuran as biologically active agentsen_US
dc.typeArticle
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