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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/123456789/2897
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-17T13:59:13Z-
dc.date.available2021-10-17T13:59:13Z-
dc.date.issued2013-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/ol4016354-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2897-
dc.description.abstractA new strategy is reported for the synthesis of 6-aminoquinoline derivatives via a tandem Povarov reaction, dihydroquinoline oxidation, and imine reduction. These products allow access to symmetrical as well as unsymmetrical tetraarylpyrido[2,3-g]quinolines, potentially useful organic electronicsen_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectTransfer reactionsen_US
dc.subjectCatalystsen_US
dc.subjectReaction productsen_US
dc.titlePovarov-Reductive Amination Cascade to Access 6-Aminoquinolines and Anthrazolinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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