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 Field	Value	Language
dc.contributor.author	Kumar, Anil	-
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2021-10-14T13:12:52Z	-
dc.date.available	2021-10-14T13:12:52Z	-
dc.date.issued	2016-11-03	-
dc.identifier.uri	https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201601329	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2840	-
dc.description.abstract	The 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.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Synthesis	en_US
dc.subject	Aryl Halides	en_US
dc.subject	Oxidative Amination	en_US
dc.title	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	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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