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

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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