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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/8622
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dc.contributor.authorDolka, C.en
dc.contributor.authorVan Hecke, K.en
dc.contributor.authorVan Meervelt, L.en
dc.contributor.authorTsoungas, P. G.en
dc.contributor.authorVan der Eycken, E. V.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:42:56Z-
dc.date.available2015-11-24T16:42:56Z-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8622-
dc.rightsDefault Licence-
dc.subjectsupported iodobenzene diacetateen
dc.subjectactivated aromatic systemsen
dc.subjectcesium fluoroxysulfateen
dc.subjectorganic-synthesisen
dc.subjectcoupling reactionen
dc.subjectperi-cyclizationen
dc.subjectbeta-naphtholen
dc.subjectfluorinationen
dc.subjectaluminaen
dc.subjectnaphthaleneen
dc.titleNovel Thermal and Microwave-Assisted Facile Route to Naphthalen-2(1H)-ones via an Oxidative Alkoxylation-Ring-Opening Protocolen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1021/Ol9008574-
heal.identifier.secondary<Go to ISI>://000268138800003-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/ol9008574-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2009-
heal.abstractSeveral novel 1,1-disubstituted-8-hydroxynaphthalen-2(1H)-ones have been efficiently synthesized via a two-step sequence from 2-hydroxy-1-naphthaldehyde oxime. The methodology involves oxidative ring closure and alkoxylation to 3a-alkoxynaphtho[1,8-de][1,2]oxazin-4(3aH)-ones, followed by thermal ring-opening. Both thermal and microwave irradiation conditions were used. A novel one-pot reaction of oxime to 8-isopropoxynaphthalene-1,7-diol using microwave irradiation is also reported.en
heal.publisherAmerican Chemical Societyen
heal.journalNameOrg Letten
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
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