A New Atropisomeric Molecular Structure for Efficient Enantiodifferentiation

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.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.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1002/anie.199306061-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/doi/10.1002/anie.199306061/abstract-
heal.journalNameAngew. Chem. Int. Ed. Engl.en
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1993-
heal.publisherVCH Verlagsgesellschaften
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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