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Ni-Catalyzed Intermolecular C(sp(3))-H Amidation Tuned by Bidentate Directing Groups

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dc.contributor.authorKim, Yeong Bum-
dc.contributor.authorWon, Joonghee-
dc.contributor.authorLee, Jeonghyo-
dc.contributor.authorKim, Junho-
dc.contributor.authorZhou, Bingwei-
dc.contributor.authorPark, Jung-Woo-
dc.contributor.authorBaik, Mu-Hyun-
dc.contributor.authorChang, Sukbok-
dc.date.accessioned2023-08-16T08:08:56Z-
dc.date.available2023-08-16T08:08:56Z-
dc.date.created2023-07-21-
dc.date.issued2021-03-
dc.identifier.issn21555435-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189283-
dc.description.abstractWe disclose herein a directing group-assisted nickel-catalyzed intermolecular C(sp(3))-H amidation using organic azides as nitrene precursors. With the installation of an electronically tailored directing group, enhanced amidation efficiency was achieved. A series of experimental and computational studies suggested that a putative nickel(III)-nitrenoid species is a key intermediate in the C-N bond-forming process.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleNi-Catalyzed Intermolecular C(sp(3))-H Amidation Tuned by Bidentate Directing Groups-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Jeonghyo-
dc.identifier.doi10.1021/acscatal.1c00070-
dc.identifier.scopusid2-s2.0-85101971244-
dc.identifier.wosid000626844200055-
dc.identifier.bibliographicCitationACS CATALYSIS, v.11, no.5, pp.3067 - 3072-
dc.relation.isPartOfACS CATALYSIS-
dc.citation.titleACS CATALYSIS-
dc.citation.volume11-
dc.citation.number5-
dc.citation.startPage3067-
dc.citation.endPage3072-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusCARBOXYLIC ANHYDRIDES-
dc.subject.keywordPlusNICKEL-
dc.subject.keywordPlusAMINATION-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusAZIDES-
dc.subject.keywordPlusBONDS-
dc.subject.keywordPlusARENES-
dc.subject.keywordPlusAMIDES-
dc.subject.keywordAuthornickel catalysis-
dc.subject.keywordAuthorC(sp(3))-H amidation-
dc.subject.keywordAuthororganic azides-
dc.subject.keywordAuthor8-aminoquinolines-
dc.subject.keywordAuthorelectronic tuning-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acscatal.1c00070-
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