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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3037
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dc.contributor.authorKumar, Dalip-
dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-27T04:20:09Z-
dc.date.available2021-10-27T04:20:09Z-
dc.date.issued2014-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/jo501119f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3037-
dc.description.abstractA straightforward method has been developed for the synthesis of aroyl-substituted imidazo-/benzimidazo-fused isoquinolines. The cascade reaction proceeds via a cross-aldol condensation of 2-(1H-imidazol-1-yl/benzimidazolyl-1-yl)-1-arylethanones and 2-bromobenzaldehyde followed by palladium-catalyzed intramolecular C–H functionalization. This approach offers a simple and efficient alternative one-pot protocol for the assembly of imidazo/benzimidazo[2,1-a]isoquinolines in moderate to good yields.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectFunctionalizationen_US
dc.subjectHydrocarbonsen_US
dc.subjectAdductsen_US
dc.titleSynthesis of aza-fused isoquinolines through domino cross-aldol condensation and palladium-catalyzed intramolecular direct arylationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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