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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3167
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
Authors: Kumar, Indresh
Keywords: Chemistry
Synthesis
Quinazolinones
Aryl Halides
Oxidative Amination
Issue Date: 3-Nov-2016
Publisher: Wiley
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.
URI: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201601329
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3167
Appears in Collections:Department of Chemistry

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