Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation

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DC Field	Value	Language
dc.contributor.author	Kumar, Anil	-
dc.contributor.author	Khungar, Bharti	-
dc.date.accessioned	2021-10-17T13:59:10Z	-
dc.date.available	2021-10-17T13:59:10Z	-
dc.date.issued	2013	-
dc.identifier.uri	https://pubs.acs.org/doi/abs/10.1021/ol401655r	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2896	-
dc.description.abstract	A ligand-free copper-catalyzed tandem azide–alkyne cycloaddition (CuAAC), Ullmann-type C–N coupling, and intramolecular direct arylation has been described. The designed strategy resulted in the synthesis of a novel trazole-fused azaheterocycle framework. The reaction gave good yields (59–77%) of 1,2,3-triazole-fused imidazo[1,2-a]pyridines in a single step.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	Catalysts	en_US
dc.subject	Hydrocarbons	en_US
dc.subject	Copper	en_US
dc.title	Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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