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

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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


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