dc.creatorMoglie, Yanina
dc.creatorMascaro, Evangelina
dc.creatorZacconi, Flavia C. M.
dc.creatorRadivoy, Gabriel
dc.date.accessioned2023-08-23T20:25:08Z
dc.date.available2023-08-23T20:25:08Z
dc.date.created2023-08-23T20:25:08Z
dc.date.issued2021
dc.identifier10.1002/slct.202101011
dc.identifier2365-6549
dc.identifierhttps://doi.org/10.1002/slct.202101011
dc.identifierhttps://repositorio.uc.cl/handle/11534/74479
dc.identifierWOS:000656953000001
dc.description.abstractCopper nanoparticles (CuNPs) supported on ZnO are highly active and selective heterogeneous catalyst for the N-arylation of cyclic and acyclic amides (Golberg coupling). The reaction conditions are mild, featuring K3PO4 as a base and N,N'-dimethylethylendiamine (DMEDA) as ligand in refluxing acetonitrile. The CuNPs/ZnO catalyst can be recovered and reused in six cycles with only little loss of activity. The methodology can be successfully scaled up to gram scale without decreasing the catalytic activity.
dc.languageen
dc.publisherWILEY-V C H VERLAG GMBH
dc.rightsacceso restringido
dc.subjectLactams
dc.subjectAmides
dc.subjectN-arylation
dc.subjectCopper nanoparticles
dc.subjectHeterogeneous catalyst
dc.subjectCoupling reactions scope
dc.subjectAryl halides
dc.subjectC-N
dc.subjectGoldberg reaction
dc.subjectAmidation
dc.subjectComplexes
dc.subjectAmination
dc.subjectMild
dc.subjectHeterocycles
dc.subjectBromides
dc.titleCopper nanoparticles supported on zinc oxide as efficient catalyst for the N-Arylation of (Hetero)cyclic and acyclic amides
dc.typeartículo


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