Alkenyl C-H insertion of a beta-disulfone iodonium ylide into flavones

dc.contributor.authorAdam, W.en
dc.contributor.authorGogonas, E. P.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:45:04Z
dc.date.available2015-11-24T16:45:04Z
dc.identifier.issn0040-4020-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8877
dc.rightsDefault Licence-
dc.subjectiodonium ylidesen
dc.subjectc-h insertionen
dc.subjectflavoneen
dc.subjectbeta-disulfoneen
dc.subjectcatalyzed intramolecular cyclopropanationsen
dc.subjectphenyliodonium ylidesen
dc.subjectorganic-synthesisen
dc.subjectpotassium-permanganateen
dc.subjectcarbenoid reactionsen
dc.subjectaurone epoxidesen
dc.subjectdimethyldioxiraneen
dc.subjectcycloadditionen
dc.subjectdecompositionen
dc.subjectrearrangementen
dc.titleAlkenyl C-H insertion of a beta-disulfone iodonium ylide into flavonesen
heal.abstractThe reaction of phenyliodonium bis(phenylsulfonyl)methylide with flavones affords insertion products into the alkenyl carbon-hydrogen bond of the flavone, presumably by an electrophilic attack of the iodonium ylide on the double bond of the flavone. (C) 2003 Elsevier Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.tet.2003.07.011-
heal.identifier.secondary<Go to ISI>://000185585800011-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040402003012985/1-s2.0-S0040402003012985-main.pdf?_tid=8450c6062f59d3092d50c18eeeafba49&acdnat=1333029999_03d4ae59c226382b825288c24b253b17-
heal.journalNameTetrahedronen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2003-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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