Brønsted acid-catalyzed hydroarylation of activated olefins

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dc.bibliographicCitation.date2015
dc.bibliographicCitation.firstPage493eng
dc.bibliographicCitation.issue1eng
dc.bibliographicCitation.lastPage496eng
dc.bibliographicCitation.volume5eng
dc.contributor.authorFleischer, Ivana
dc.contributor.authorPospech, Jola
dc.date.accessioned2022-06-24T06:40:48Z
dc.date.available2022-06-24T06:40:48Z
dc.date.issued2014
dc.description.abstractA mild, regiospecific Brønsted acid-catalyzed hydroarylation of activated olefins, capable of the formation of quinone methide-like intermediates, has been investigated. Variously substituted 2- and 4-vinylphenols, 4-vinylaniline or 6-vinyl-naphthalen-2-ol were successfully implemented in a sequential protonation and Friedel–Crafts-type alkylation reaction of electron-rich arenes.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/9264
dc.identifier.urihttps://doi.org/10.34657/8302
dc.language.isoengeng
dc.publisherLondon : RSC Publishingeng
dc.relation.doihttps://doi.org/10.1039/c4ra13647k
dc.relation.essn2046-2069
dc.relation.ispartofseriesRSC Advances : an international journal to further the chemical sciences 5 (2015), Nr. 1eng
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subjectOlefinseng
dc.subjectActivated olefinseng
dc.subjectAlkylation reactionseng
dc.subjectElectron-rich areneseng
dc.subjectFriedel-Craftseng
dc.subjectHydroarylationeng
dc.subjectQuinone methideeng
dc.subjectRegiospecificeng
dc.subjectCatalysiseng
dc.subject.ddc540eng
dc.titleBrønsted acid-catalyzed hydroarylation of activated olefinseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleRSC Advances : an international journal to further the chemical scienceseng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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