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dc.contributor.authorNitha, P R-
dc.contributor.authorManu, M-
dc.contributor.authorJoseph-
dc.contributor.authorGreeshma, Gopalan-
dc.contributor.authorMaiti, K K-
dc.contributor.authorRadhakrishnan, K V-
dc.contributor.authorDas, Parthasarathi-
dc.date.accessioned2018-10-15T11:19:00Z-
dc.date.available2018-10-15T11:19:00Z-
dc.date.issued2018-08-
dc.identifier.citationOrganic & Biomolecular Chemistry, 16(35):6430–6437en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3273-
dc.description.abstractA palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically potent 2-amidoimidazopyridine scaffolds. The aminocarbonylation reaction was found to be general with a range of amines and substituted imidazopyridines. Preliminary biological evaluation of cytotoxicity on selected examples provides scope for future investigations.en_US
dc.language.isoenen_US
dc.publisherThe Royal Society of Chemistryen_US
dc.titleChloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo [1,2-a]pyridinesen_US
dc.typeArticleen_US
Appears in Collections:2018

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