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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/123456789/2859
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-17T13:56:28Z-
dc.date.available2021-10-17T13:56:28Z-
dc.date.issued2015-
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.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.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
Appears in Collections:Department of Chemistry

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