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dc.contributor.authorAdam, W.en
dc.contributor.authorHadjiarapoglou, L.en
dc.date.accessioned2015-11-24T16:56:20Z-
dc.date.available2015-11-24T16:56:20Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10420-
dc.rightsDefault Licence-
dc.subjectEpoxidationen
dc.subjectDioxirane, dimethyl-en
dc.subjectEnol ethers, Ξ²-oxoen
dc.titleDimethyldioxirane epoxidation of Ξ²-oxo enol ethersen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/cber.19901231022-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/doi/10.1002/cber.19901231022/abstract-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1990-
heal.abstractThe synthesis of the epoxides 2a-f by epoxidation of the Ξ²-oxo enol ethers 2,2-dimethyl-3(2H)-furanone (1a), (Z)-2(ethoxymethylene)cyclohexanone (1b), and 3-alkoxy-5,5-dimethyl-2-cyclohexenones 1c-f with dimethyldioxirane is reported. These labile epoxides (stable below 0Β°C) were isolated and characterized spectroscopically (IR, 1H, and 13C NMR). Warming up to room temperature led to decomposition to afford complex product mixtures. When the epoxidation of 3-ethoxy-5,5-dimethyl-2-cyclohexenone (1c) was conducted above 0Β°C, the epoxide 2c afforded the rearrangement product 3-ethoxy-2-hydroxy-5,5-dimethyl-2-cyclohexenone (3).en
heal.publisherWILEY-VCH Verlagen
heal.journalNameChemische Berichteen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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