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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