DSpace Repository

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

Show simple item record

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


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account