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

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2021-10-17T13:56:28Z
dc.date.available 2021-10-17T13:56:28Z
dc.date.issued 2015
dc.identifier.uri https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560177
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2859
dc.description.abstract A 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.iso en en_US
dc.publisher Thieme en_US
dc.subject Chemistry en_US
dc.subject C–H activation en_US
dc.subject C–C bond formation en_US
dc.subject Direct arylation en_US
dc.subject Palladium catalysis en_US
dc.title Synthesis of Imidazo[1,2-f]phenanthridines through Palladium-Catalyzed Intramolecular C–C Bond Formation en_US
dc.type Article en_US


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