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dc.contributor.authorHan, Seo-Jung-
dc.contributor.authorCavitt, Marchello A.-
dc.contributor.authorStoltz, Brian M.-
dc.date.accessioned2024-01-19T15:00:54Z-
dc.date.available2024-01-19T15:00:54Z-
dc.date.created2021-09-04-
dc.date.issued2021-05-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/117101-
dc.description.abstractEight-membered nitrogen-containing heterocycles were straightforwardly produced by a nickel-catalyzed cycloetherification and subsequent Claisen rearrangement of secondary and tertiary alcohols. In particular, a one-pot transformation was achieved with tertiary alcohols in moderate to good yields. This operationally simple reaction is tolerant of many functional groups and applicable to the synthesis of various medium-sized ring nitrogen-containing heterocycles.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleA Synthetic Strategy toward Eight-Membered Cyclic Amines by Cycloetherification and Claisen Rearrangement-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.1c00763-
dc.description.journalClass1-
dc.identifier.bibliographicCitationOrganic Letters, v.23, no.9, pp.3300 - 3303-
dc.citation.titleOrganic Letters-
dc.citation.volume23-
dc.citation.number9-
dc.citation.startPage3300-
dc.citation.endPage3303-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000649477300014-
dc.identifier.scopusid2-s2.0-85105117171-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
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KIST Article > 2021
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