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Copper-catalyzed synthesis of quinoline derivatives via tandem Knoevenagel condensation, amination and cyclization

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dc.contributor.author Kumar, Anil
dc.contributor.author Kumar, Dalip
dc.date.accessioned 2021-10-14T13:13:25Z
dc.date.available 2021-10-14T13:13:25Z
dc.date.issued 2016
dc.identifier.uri https://pubs.rsc.org/en/Content/ArticleLanding/RA/2016/C6RA03798D
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2847
dc.description.abstract A novel regioselective synthesis of 2-aminoquinolines and 2-arylquinoline-3-carbonitriles is described via copper-mediated tandem reaction. Formation of substituted quinolines involves Knoevenagel condensation of ortho-bromobenzaldehyde with active methylene nitriles followed by copper-catalyzed reductive amination and intramolecular cyclization. en_US
dc.language.iso en en_US
dc.publisher RSC en_US
dc.subject Chemistry en_US
dc.subject Copper-Catalyzed en_US
dc.subject Knoevenagel condensation en_US
dc.title Copper-catalyzed synthesis of quinoline derivatives via tandem Knoevenagel condensation, amination and cyclization en_US
dc.type Article en_US


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