Ni-Catalyzed Intermolecular C(sp3)-H Amidation Tuned by Bidentate Directing Groups
DC Field | Value | Language |
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dc.contributor.author | Yeong Bum Kim | - |
dc.contributor.author | Joonghee Won | - |
dc.contributor.author | Jeonghyo Lee | - |
dc.contributor.author | Junho Kim | - |
dc.contributor.author | Bingwei Zhou | - |
dc.contributor.author | Jung-Woo Park | - |
dc.contributor.author | Mu-Hyun Baik | - |
dc.contributor.author | Sukbok Chang | - |
dc.date.accessioned | 2021-04-01T01:30:08Z | - |
dc.date.accessioned | 2021-04-01T01:30:08Z | - |
dc.date.available | 2021-04-01T01:30:08Z | - |
dc.date.available | 2021-04-01T01:30:08Z | - |
dc.date.created | 2021-03-24 | - |
dc.date.issued | 2021-03-05 | - |
dc.identifier.issn | 2155-5435 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/9294 | - |
dc.description.abstract | We 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.language | 영어 | - |
dc.publisher | American Chemical Society | - |
dc.title | Ni-Catalyzed Intermolecular C(sp3)-H Amidation Tuned by Bidentate Directing Groups | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000626844200055 | - |
dc.identifier.scopusid | 2-s2.0-85101971244 | - |
dc.identifier.rimsid | 75118 | - |
dc.contributor.affiliatedAuthor | Yeong Bum Kim | - |
dc.contributor.affiliatedAuthor | Joonghee Won | - |
dc.contributor.affiliatedAuthor | Jeonghyo Lee | - |
dc.contributor.affiliatedAuthor | Junho Kim | - |
dc.contributor.affiliatedAuthor | Bingwei Zhou | - |
dc.contributor.affiliatedAuthor | Jung-Woo Park | - |
dc.contributor.affiliatedAuthor | Mu-Hyun Baik | - |
dc.contributor.affiliatedAuthor | Sukbok Chang | - |
dc.identifier.doi | 10.1021/acscatal.1c00070 | - |
dc.identifier.bibliographicCitation | ACS Catalysis, v.11, no.5, pp.3067 - 3072 | - |
dc.relation.isPartOf | ACS Catalysis | - |
dc.citation.title | ACS Catalysis | - |
dc.citation.volume | 11 | - |
dc.citation.number | 5 | - |
dc.citation.startPage | 3067 | - |
dc.citation.endPage | 3072 | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.subject.keywordAuthor | 8-aminoquinolines | - |
dc.subject.keywordAuthor | C(sp3)-H amidation | - |
dc.subject.keywordAuthor | electronic tuning | - |
dc.subject.keywordAuthor | nickel catalysis | - |
dc.subject.keywordAuthor | organic azides | - |