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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/123456789/15541
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dc.contributor.authorKumar, Indresh-
dc.date.accessioned2024-09-12T04:10:42Z-
dc.date.available2024-09-12T04:10:42Z-
dc.date.issued2023-07-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.3c01092-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15541-
dc.description.abstractA straightforward method has been developed to synthesize 2-aryl-3-(2-aminoaryl) quinoxalines from 2-arylindoles and 1,2-diaminoarenes under mild electrochemical conditions. The reaction proceeds through in situ generations of 2-arylindole-3-ones under electrochemical oxidative dearomatization of 2-arylindoles, followed by a ring opening-cyclization sequence with 1,2-diaminoarenes. A series of 2-aryl-3-(2-aminoaryl) quinoxalines have been prepared with moderate to good yields (up to 75%).en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectAtmospheric chemistryen_US
dc.subjectElectrochemical synthesisen_US
dc.subjectElectrodesen_US
dc.subjectFossil fuelsen_US
dc.subjectPurificationen_US
dc.titleElectrochemical Synthesis of 2-Aryl-3-(2-aminoaryl)quinoxalines via Oxidative Dearomatization/Ring-Opening/Cyclization Cascade Sequence of 2-Arylindoles with 1,2-Diaminoarenesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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