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dc.contributor.authorAdam, W.en
dc.contributor.authorBialas, J.en
dc.contributor.authorHadjiarapoglou, L.en
dc.contributor.authorPatonay, T.en
dc.date.accessioned2015-11-24T16:56:23Z-
dc.date.available2015-11-24T16:56:23Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10431-
dc.rightsDefault Licence-
dc.titleDirect Epoxidation of E-2"™-Hydroxychalcones by Dimethyldioxiraneen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1055/s-1992-34184-
heal.identifier.secondaryhttps://docs.google.com/file/d/0BxfLht5wJUEINzUyMmM5Y2ItYzQ3My00ZmE4LTgwZDEtYWJlZDk2YTc4N2Fj/edit?hl=en-
heal.identifier.secondaryhttps://www.thieme-connect.com/ejournals/abstract/10.1055/s-1992-34184-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1992-
heal.abstractThe synthesis of Ξ±,Ξ²-epoxy-2'-hydroxychalcones (3-aryl-2,3-epoxy-1-(2-hydroxyaryl)propanones) 2 by direct epoxidation of (E)-2'-hydroxychalcones [(E)-3-aryl-1-(2-hydroxyaryl)propenone] 1 with dimethyldioxirane at subambient temperatures is reported. These acid- and base-sensitive epoxides, which have been hitherto difficult to prepare, were isolated in excellent yields and were completely characterized by spectral and microanalytical data. The now readily available 2'-hydroxy substituted chalcone oxides may serve as convenient precursors to flavonoid-type natural products.en
heal.journalNameSynthesisen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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