Ni-Catalyzed Intermolecular C(sp3)-H Amidation Tuned by Bidentate Directing Groups

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dc.contributor.authorKim, Yeong Bumko
dc.contributor.authorWon, Joongheeko
dc.contributor.authorLee, Jeonghyoko
dc.contributor.authorKim, Junhoko
dc.contributor.authorZhou, Bingweiko
dc.contributor.authorPark, Jung-Wooko
dc.contributor.authorBaik, Mu-Hyunko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2021-12-24T06:44:47Z-
dc.date.available2021-12-24T06:44:47Z-
dc.date.created2021-12-23-
dc.date.created2021-12-23-
dc.date.created2021-12-23-
dc.date.created2021-12-23-
dc.date.issued2021-03-
dc.identifier.citationACS CATALYSIS, v.11, no.5, pp.3067 - 3072-
dc.identifier.issn2155-5435-
dc.identifier.urihttp://hdl.handle.net/10203/291131-
dc.description.abstractWe disclose herein a directing group-assisted nickel-catalyzed intermolecular C(sp3)-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.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleNi-Catalyzed Intermolecular C(sp3)-H Amidation Tuned by Bidentate Directing Groups-
dc.typeArticle-
dc.identifier.wosid000626844200055-
dc.identifier.scopusid2-s2.0-85101971244-
dc.type.rimsART-
dc.citation.volume11-
dc.citation.issue5-
dc.citation.beginningpage3067-
dc.citation.endingpage3072-
dc.citation.publicationnameACS CATALYSIS-
dc.identifier.doi10.1021/acscatal.1c00070-
dc.contributor.localauthorBaik, Mu-Hyun-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.nonIdAuthorKim, Yeong Bum-
dc.contributor.nonIdAuthorLee, Jeonghyo-
dc.contributor.nonIdAuthorKim, Junho-
dc.contributor.nonIdAuthorZhou, Bingwei-
dc.contributor.nonIdAuthorPark, Jung-Woo-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthornickel catalysis-
dc.subject.keywordAuthorC(sp(3))-H amidation-
dc.subject.keywordAuthororganic azides-
dc.subject.keywordAuthor8-aminoquinolines-
dc.subject.keywordAuthorelectronic tuning-
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