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DC Field | Value | Language |
---|---|---|
dc.citation.endPage | 2766 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 2763 | - |
dc.citation.title | JOURNAL OF ORGANIC CHEMISTRY | - |
dc.citation.volume | 75 | - |
dc.contributor.author | Hudnall, Todd W. | - |
dc.contributor.author | Moorhead, Eric J. | - |
dc.contributor.author | Gusev, Dmitry G. | - |
dc.contributor.author | Bielawski, Christopher W. | - |
dc.date.accessioned | 2023-12-22T07:09:52Z | - |
dc.date.available | 2023-12-22T07:09:52Z | - |
dc.date.created | 2020-07-13 | - |
dc.date.issued | 2010-04 | - |
dc.description.abstract | Treatment of an N-heterocyclic carbene that features two amide groups N-bound to the carbene nucleus with various organic isocyanides afforded a new class of ketenimines in yields of up to 96% (isolated). DFT analyses revealed that the carbene exhibits a unique, low-lying LUMO, which may explain the atypical reactivity observed. | - |
dc.identifier.bibliographicCitation | JOURNAL OF ORGANIC CHEMISTRY, v.75, no.8, pp.2763 - 2766 | - |
dc.identifier.doi | 10.1021/jo100427g | - |
dc.identifier.issn | 0022-3263 | - |
dc.identifier.scopusid | 2-s2.0-77951011202 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/33245 | - |
dc.identifier.url | https://pubs.acs.org/doi/10.1021/jo100427g | - |
dc.identifier.wosid | 000276556600046 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | N,N '-Diamidoketenimines via Coupling of Isocyanides to an N-Heterocyclic Carbene | - |
dc.type | Article | - |
dc.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | STABLE CARBENES | - |
dc.subject.keywordPlus | DIMERIZATION | - |
dc.subject.keywordPlus | STABILITY | - |
dc.subject.keywordPlus | CHEMISTRY | - |
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