Nickel/briphos-catalyzed transamidation of unactivated tertiary amides

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dc.contributor.authorYang, Dahyeonko
dc.contributor.authorShin, Taeilko
dc.contributor.authorKim, Hyunwooko
dc.contributor.authorLee, Sunwooko
dc.date.accessioned2021-03-26T02:32:48Z-
dc.date.available2021-03-26T02:32:48Z-
dc.date.created2020-08-31-
dc.date.issued2020-08-
dc.identifier.citationORGANIC & BIOMOLECULAR CHEMISTRY, v.18, no.31, pp.6053 - 6057-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10203/281941-
dc.description.abstractThe transamidation of tertiary amides was achievedvianickel catalysis in combination with briphos ligands.N-Methyl-N-phenylbenzamide derivatives reacted with primary amines in the presence of NiCl2/briphos L4 to provide the transamidated products in moderate to good yields. Primary aromatic amines delivered higher product yields than aliphatic amines.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleNickel/briphos-catalyzed transamidation of unactivated tertiary amides-
dc.typeArticle-
dc.identifier.wosid000558540500006-
dc.identifier.scopusid2-s2.0-85089407878-
dc.type.rimsART-
dc.citation.volume18-
dc.citation.issue31-
dc.citation.beginningpage6053-
dc.citation.endingpage6057-
dc.citation.publicationnameORGANIC & BIOMOLECULAR CHEMISTRY-
dc.identifier.doi10.1039/d0ob01271h-
dc.contributor.localauthorKim, Hyunwoo-
dc.contributor.nonIdAuthorYang, Dahyeon-
dc.contributor.nonIdAuthorLee, Sunwoo-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusN-C CLEAVAGE-
dc.subject.keywordPlusMETAL-FREE TRANSAMIDATION-
dc.subject.keywordPlusPRIMARY CARBOXAMIDES-
dc.subject.keywordPlusSECONDARY AMIDES-
dc.subject.keywordPlusCARBOXYLIC-ACIDS-
dc.subject.keywordPlusAMIDATION-
dc.subject.keywordPlusESTERIFICATION-
dc.subject.keywordPlusCARBONYLATION-
dc.subject.keywordPlusAMINES-
dc.subject.keywordPlusESTERS-
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