Synthesis of Quinazolinones, Imidazo[1,2-c]quinazolines and Imidazo[4,5-c]quinolines through Tandem Reductive Amination of Aryl Halides and Oxidative Amination of C(sp3)–H Bonds

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dc.contributor.authorKumar, Anil
dc.contributor.authorKumar, Indresh
dc.date.accessioned2021-10-14T13:12:52Z
dc.date.available2021-10-14T13:12:52Z
dc.date.issued2016-11-03
dc.description.abstractThe synthesis of quinazolinones, imidazo[1,2-c]quinazolines and imidazo[4,5-c]quinolones has been achieved through a multicomponent copper-catalyzed reaction using easily available sodium azide as a nitrogen source, and DMA (N,N-dimethylacetamide) as a one-carbon source. N-Fused heterocycles were obtained in good to excellent yields, and the reaction is suitable for gram-scale synthesis.en_US
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201601329
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2840
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectAryl Halidesen_US
dc.subjectOxidative Aminationen_US
dc.titleSynthesis of Quinazolinones, Imidazo[1,2-c]quinazolines and Imidazo[4,5-c]quinolines through Tandem Reductive Amination of Aryl Halides and Oxidative Amination of C(sp3)–H Bondsen_US
dc.typeArticleen_US

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