Modular Tuning of Electrophilic Reactivity of Iridium Nitrenoids for the Intermolecular Selective α-Amidation of β-Keto Esters
DC Field | Value | Language |
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dc.contributor.author | Minhan Lee | - |
dc.contributor.author | Hoimin Jung | - |
dc.contributor.author | Dongwook Kim | - |
dc.contributor.author | Jung-Woo Park | - |
dc.contributor.author | Sukbok Chang | - |
dc.date.accessioned | 2020-12-22T02:57:08Z | - |
dc.date.accessioned | 2020-12-22T02:57:08Z | - |
dc.date.available | 2020-12-22T02:57:08Z | - |
dc.date.available | 2020-12-22T02:57:08Z | - |
dc.date.created | 2020-09-09 | - |
dc.date.issued | 2020-07 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/7759 | - |
dc.description.abstract | © 2020 American Chemical Society We report herein an Ir-catalyzed intermolecular amino group transfer to β-keto esters (amides) to access α-aminocarbonyl products with excellent chemoselectivity. The key strategy was to engineer electrophilicity of the putative Ir-nitrenoids by tuning electronic property of the κ2-N,O chelating ligands, thus facilitating nucleophilic addition of enol π-bonds of 1,3-dicarbonyl substrates | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | C-H AMINATION | - |
dc.subject | CATALYZED AZIRIDINATION | - |
dc.subject | GAMMA-LACTAMS | - |
dc.subject | BONDS | - |
dc.subject | FUNCTIONALIZATION | - |
dc.subject | DERIVATIVES | - |
dc.subject | STRATEGY | - |
dc.subject | ACCESS | - |
dc.title | Modular Tuning of Electrophilic Reactivity of Iridium Nitrenoids for the Intermolecular Selective α-Amidation of β-Keto Esters | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000551495700010 | - |
dc.identifier.scopusid | 2-s2.0-85088177297 | - |
dc.identifier.rimsid | 72827 | - |
dc.contributor.affiliatedAuthor | Minhan Lee | - |
dc.contributor.affiliatedAuthor | Hoimin Jung | - |
dc.contributor.affiliatedAuthor | Dongwook Kim | - |
dc.contributor.affiliatedAuthor | Jung-Woo Park | - |
dc.contributor.affiliatedAuthor | Sukbok Chang | - |
dc.identifier.doi | 10.1021/jacs.0c04344 | - |
dc.identifier.bibliographicCitation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.142, no.28, pp.11999 - 12004 | - |
dc.citation.title | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.citation.volume | 142 | - |
dc.citation.number | 28 | - |
dc.citation.startPage | 11999 | - |
dc.citation.endPage | 12004 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | C-H AMINATION | - |
dc.subject.keywordPlus | CATALYZED AZIRIDINATION | - |
dc.subject.keywordPlus | GAMMA-LACTAMS | - |
dc.subject.keywordPlus | BONDS | - |
dc.subject.keywordPlus | FUNCTIONALIZATION | - |
dc.subject.keywordPlus | DERIVATIVES | - |
dc.subject.keywordPlus | STRATEGY | - |
dc.subject.keywordPlus | ACCESS | - |