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Nickel-Catalyzed Double Deoxygenative C-N Coupling of Acyloxyamines

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dc.contributor.authorAli, Kashif-
dc.contributor.authorCho, Eun Jin-
dc.date.accessioned2024-07-12T06:00:43Z-
dc.date.available2024-07-12T06:00:43Z-
dc.date.issued2024-06-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74727-
dc.description.abstractA double deoxygenative C-N coupling protocol has been developed by employing acyloxyamines through N-O bond activation. The C-N bond formation under mild reaction conditions, employing NiCl2 as the catalyst and cataCXiumA as a ligand, results in the production of a diverse array of alkylated secondary or tertiary amines, including heterocyclic amines. This method introduces a novel catalytic strategy that emphasizes the versatility of nickel-catalyzed reactions, extending beyond traditional synthetic boundaries.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleNickel-Catalyzed Double Deoxygenative C-N Coupling of Acyloxyamines-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.4c01758-
dc.identifier.bibliographicCitationOrganic letters, v.26, no.24, pp 5192 - 5195-
dc.description.isOpenAccessN-
dc.identifier.wosid001243965900001-
dc.identifier.scopusid2-s2.0-85196114547-
dc.citation.endPage5195-
dc.citation.number24-
dc.citation.startPage5192-
dc.citation.titleOrganic letters-
dc.citation.volume26-
dc.type.docTypeArticle; Early Access-
dc.publisher.location미국-
dc.subject.keywordPlusAMIDES-
dc.subject.keywordPlusHYDROGENATION-
dc.subject.keywordPlusREDUCTION-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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