Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9461
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dc.contributor.authorNaxakis, G.en
dc.contributor.authorSofou, P.en
dc.contributor.authorElemes, Y.en
dc.date.accessioned2015-11-24T16:49:18Z-
dc.date.available2015-11-24T16:49:18Z-
dc.identifier.issn1536-383X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9461-
dc.rightsDefault Licence-
dc.subjectfullerenesen
dc.subjectpyrrolidinesen
dc.subjectcycloadditionen
dc.subjectazomethineen
dc.subject1,3-dipolar cycloaddition reactionen
dc.subjectbuckminsterfullerene c-60en
dc.subjectaddition-reactionsen
dc.subjectamino-acidsen
dc.subjectfulleropyrrolidinesen
dc.subjectfullerenesen
dc.subjectesteren
dc.titleSynthesis of novel 3,4-dihydro-2H-pyrrolo[60]fullerene derivatives bearing an alkylsulfanyl substituenten
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1081/Fst-200032892-
heal.identifier.secondary<Go to ISI>://000225614900006-
heal.identifier.secondaryhttp://www.tandfonline.com/doi/pdf/10.1081/FST-200032892-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2004-
heal.abstractC-60 reacts thermally with azomethine ylides of glycine imines, in methyl ester and free acid form, bearing two alkylsulfanyl groups to give dihydro-pyrrolo[60]fullerene derivatives 2 and 5a, respectively, in a 1,3-dipolar cycloaddition reaction. The yields of products were found to depend strongly on acidic conditions applied and the size of the alkylsulfanyl substituent. Graphics. a: R=Me, b: R=Et, a R=Pro, d: R=i-Pro.en
heal.publisherTaylor & Francisen
heal.journalNameFullerenes Nanotubes and Carbon Nanostructuresen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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