Synthesis of the 2,3-epoxide of the 2,3-dimethylbenzo[b]furan, the proposed ultimate mutagen of the benzofuran dioxetanes

dc.contributor.authorAdam, W.en
dc.contributor.authorHadjiarapoglou, L.en
dc.contributor.authorMosandl, T.en
dc.contributor.authorSaha-MΞΏller, C.en
dc.contributor.authorWild, B.en
dc.date.accessioned2015-11-24T16:49:20Z
dc.date.available2015-11-24T16:49:20Z
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9469
dc.rightsDefault Licence-
dc.titleSynthesis of the 2,3-epoxide of the 2,3-dimethylbenzo[b]furan, the proposed ultimate mutagen of the benzofuran dioxetanesen
heal.abstractDioxetanes can be precursors for mutagenic epoxides"”this provocative hypothesis is the result of this study. Epoxidation of the benzofurans 1 with dimethyldioxirane and deoxygenation of the benzofuran dioxetanes 3 with dimethyl sulfides allows for the first time the synthesis of labile furanepoxides 2. Compounds 2 and 3 are strongly mutagenic in the histidine-auxotrophic Salmonella typhimurium strain TA 100. X = H, Ac.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1002/anie.199102001-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/doi/10.1002/anie.199102001/abstract-
heal.journalNameAngewandte Chemie International Edition in Englishen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1991-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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