[3+2] cycloaddition of phenyliodonium bis(arylsulfonyl)methylides with alpha,beta-enones

dc.contributor.authorAdam, W.en
dc.contributor.authorGogonas, E. P.en
dc.contributor.authorNyxas, L. A.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:45:00Z
dc.date.available2015-11-24T16:45:00Z
dc.identifier.issn0039-7881-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8865
dc.rightsDefault Licence-
dc.subjectiodonium ylideen
dc.subjectchalconesen
dc.subjectdiastereoselectivityen
dc.subjectregioselectivityen
dc.subject1,2,3-trisubstituted indanesen
dc.subjectalpha,beta-unsaturated ketonesen
dc.subjectrearrangementen
dc.subjectsulfonesen
dc.subjectfacileen
dc.subjectepoxidationen
dc.subjectalkenesen
dc.subjectestersen
dc.subjectylidesen
dc.title[3+2] cycloaddition of phenyliodonium bis(arylsulfonyl)methylides with alpha,beta-enonesen
heal.abstractThe [3+2] cycloaddition of phenyliodonium bis(arylsulfonyl)methylides to alpha,beta-enones affords exclusively trans,trans-configured 1-(arylsulfonyl)-2-aroyl-3-arylindanes. The initial electrophilic attack of the iodonium ylide on the alkenyl double bond of the chalcone, followed by cyclization of the dipolar species, and subsequent ejection of iodobenzene and sulfur dioxide, stereoselectively affords the indane cycloadduct.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1055/s-2007-990801-
heal.identifier.secondary<Go to ISI>://000250719600019-
heal.identifier.secondaryhttps://www.thieme-connect.de/ejournals/pdf/synthesis/doi/10.1055/s-2007-990801.pdf-
heal.journalNameSynthesis-Stuttgarten
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2007-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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