Synthesis of Imidazo[1,2-f]phenanthridines through Palladium-Catalyzed Intramolecular C–C Bond Formation

dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-17T13:56:28Z
dc.date.available2021-10-17T13:56:28Z
dc.date.issued2015
dc.description.abstractA simple and convenient approach is developed for the synthesis of the imidazo[1,2-f]phenanthridine framework via post-functionalization of imidazoles obtained through four-component reactions of 1,2-dicarbonyl compounds, anilines, aldehydes and ammonium acetate. The methodology involves palladium-catalyzed direct arylation through sp2 C–H activation. The reported procedure delivers good to high yields of imidazo[1,2-f]phenanthridine derivatives (58–94%) starting from readily available precursors.en_US
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560177
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2859
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjectChemistryen_US
dc.subjectC–H activationen_US
dc.subjectC–C bond formationen_US
dc.subjectDirect arylationen_US
dc.subjectPalladium catalysisen_US
dc.titleSynthesis of Imidazo[1,2-f]phenanthridines through Palladium-Catalyzed Intramolecular C–C Bond Formationen_US
dc.typeArticleen_US

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