Please use this identifier to cite or link to this item: https://hdl.handle.net/10321/2293
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dc.contributor.authorSandeep, C.en_US
dc.contributor.authorPadmashali, Basavarajen_US
dc.contributor.authorKulkarni, Rashmi S.en_US
dc.contributor.authorVenugopala, Katharigatta Narayanaswamyen_US
dc.contributor.authorVenugopala, Rashmien_US
dc.contributor.authorOdhav, Bhartien_US
dc.date.accessioned2017-02-22T09:53:41Z-
dc.date.available2017-02-22T09:53:41Z-
dc.date.issued2016-
dc.identifier.citationSandeep, C.. et al. 2016. Synthesis and characterization of Ethyl 7-Acetyl-2-substituted 3-(substituted benzoyl)indolizine-1-carboxylates for in vitro anticancer activity. Asian Journal of Chemistry. 28(5): 1043-1048.en_US
dc.identifier.issn0970-7077-
dc.identifier.urihttp://hdl.handle.net/10321/2293-
dc.description.abstractEfficient synthesis of a series of novel indolizines (2a-r) has been achieved by reaction between 4-acetyl-1-[2-(substituted phenyl)-2-oxoethyl]pyridin-1-ium bromide and substituted alkynes in presence of anhydrous potassium carbonate in dimethyl formamide medium. The title compounds have been characterized by spectroscopic techniques and elemental analysis. Selected compounds 2b, 2h, 2i, 2q and 2r have been screened for in vitro anticancer activity using adriamycin as positive control and it was found that compounds 2b, 2q and 2r have shown significant anticancer activity.en_US
dc.format.extent6 pen_US
dc.language.isoenen_US
dc.publisherChemic Publishing Companyen_US
dc.relation.ispartofAsian Journal of Chemistryen_US
dc.subjectAnticanceren_US
dc.subjectCharacterizationen_US
dc.subjectIndolizine analoguesen_US
dc.subjectSynthesisen_US
dc.titleSynthesis and characterization of Ethyl 7-Acetyl-2-substituted 3-(substituted benzoyl)indolizine-1-carboxylates for in vitro anticancer activityen_US
dc.typeArticleen_US
dc.publisher.urihttp://www.asianjournalofchemistry.co.in/User/ViewFreeArticle.aspx?ArticleID=28_5_24en_US
dc.dut-rims.pubnumDUT-005576en_US
dc.identifier.doihttps://doi.org/10.14233/ajchem.2016.19582-
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item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeArticle-
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