Facile preparation of bicyclo[2.2.2]octenone derivatives via Diels-Alder cycloadditions of in situ-generated masked o-benzoquinones

dc.contributor.authorKalogiros, C.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:58:25Z
dc.date.available2015-11-24T16:58:25Z
dc.identifier.issn0040-4020-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10685
dc.rightsDefault Licence-
dc.subject2,2-dimethoxycyclohexa-3,5-dienoneen
dc.subjectretro-diels-alder/diels-alderen
dc.subjectcycloadditionen
dc.subjectmasked o-benzoquinoneen
dc.subjectphenol oxidationen
dc.subjectstereoselective-synthesisen
dc.subjectorthoquinone monoketalsen
dc.subjectcis-decalinsen
dc.subjectefficienten
dc.subjectoxidationen
dc.subjectcyclohexa-2,4-dienonesen
dc.subject2-methoxyphenolsen
dc.subjectaciden
dc.subjectheterocyclesen
dc.subjecttriquinanesen
dc.titleFacile preparation of bicyclo[2.2.2]octenone derivatives via Diels-Alder cycloadditions of in situ-generated masked o-benzoquinonesen
heal.abstractDiels-Alder cycloadditions of in situ-generated, substituted 2,2-dimethoxycyclohexa-3,5-dienones with olefinic dienophiles resulted in the development of an efficient method for the preparation of highly functionalized bicyclo[2.2.2]oct-5-en-2-ones with good to excellent yields. (C) 2011 Elsevier Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.tet.2011.03.018-
heal.identifier.secondary<Go to ISI>://000290075200009-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040402011003437/1-s2.0-S0040402011003437-main.pdf?_tid=620f1de1857e0d95886be0c7c2fb01c5&acdnat=1333030043_beedca865d8f240f29232dc272664d4f-
heal.journalNameTetrahedronen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2011-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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