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dc.contributor.authorAdam, W.en
dc.contributor.authorHadjiarapoglou, L.en
dc.contributor.authorPeters, K.en
dc.contributor.authorSauter, M.en
dc.date.accessioned2015-11-24T16:56:19Z-
dc.date.available2015-11-24T16:56:19Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10416-
dc.rightsDefault Licence-
dc.titleQuinone Methides, and Benzoxetenesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1021/ja00072a012-
heal.identifier.secondaryhttp://pubs.acs.org/doi/abs/10.1021/ja00072a012-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1993-
heal.abstractLow-temperature oxidation of the four possible regioisomeric methoxy-substituted benzofurans 1 by dimethyldioxirane afforded the rather labile epoxides 2, which are in equilibrium with their equally labile quinone methides 3 through reversible valence isomerization. Photochemical cyclization of the latter afforded the hitherto unknown benzoxetenes 4, which are sufficiently persistent at subambient temperatures to permit spectral characterization. The labile oxetenes 4 slowly revert to the same equilibrium mixtures of the epoxides 2 and quinone methides 3 as are obtained in the dioxirane epoxidation of the benzofurans 1. The mutual transformations of the benzofuran epoxides 2, quinone methides 3, and benzoxetenes 4 include thermal isomerization to the allylic alcohols S and their ring-opened tautomers S"™, nucleophilic trapping in the form of the methanol adducts 6 and their ring-opened tautomers 6"™, inverse Diels-Alder reaction to the [4 + 21 cycloadducts 7, and the 1,3-dipolar cycloaddition products 8 with tetracyanoethylene (TCNE).en
heal.publisherAmerican Chemical Societyen
heal.journalNameJ. Am. Chem. Soc.en
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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