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BielawskiChristopher W

Bielawski, Christopher W.
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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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