Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/10434
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dc.contributor.authorWeber, E.en
dc.contributor.authorSkobridis, K.en
dc.contributor.authorWierig, A.en
dc.contributor.authorStathi, S.en
dc.contributor.authorNassimbeni, L. R.en
dc.contributor.authorNiven, M. L.en
dc.date.accessioned2015-11-24T16:56:24Z-
dc.date.available2015-11-24T16:56:24Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10434-
dc.rightsDefault Licence-
dc.titleA New Atropisomeric Molecular Structure for Efficient Enantiodifferentiationen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/anie.199306061-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/doi/10.1002/anie.199306061/abstract-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1993-
heal.abstractEnantioselective clathrate formation and sorption is possible with the enantiomers of the novel atropisomer 1. Racemic 1 is easily accessible from 2,2'-dibromophenyl and fluorenone; the (S)-(+) enantiomer can be obtained pure with (β�’)-fenchone on formation of the sparingly soluble inclusion complex. Other potential applications are envisaged for these atropisomers in analysis and in asymmetric synthesis.en
heal.publisherVCH Verlagsgesellschaften
heal.journalNameAngew. Chem. Int. Ed. Engl.en
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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