A New Atropisomeric Molecular Structure for Efficient Enantiodifferentiation
dc.contributor.author | Weber, E. | en |
dc.contributor.author | Skobridis, K. | en |
dc.contributor.author | Wierig, A. | en |
dc.contributor.author | Stathi, S. | en |
dc.contributor.author | Nassimbeni, L. R. | en |
dc.contributor.author | Niven, M. L. | en |
dc.date.accessioned | 2015-11-24T16:56:24Z | |
dc.date.available | 2015-11-24T16:56:24Z | |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/10434 | |
dc.rights | Default Licence | - |
dc.title | A New Atropisomeric Molecular Structure for Efficient Enantiodifferentiation | en |
heal.abstract | Enantioselective 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.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.primary | 10.1002/anie.199306061 | - |
heal.identifier.secondary | http://onlinelibrary.wiley.com/doi/10.1002/anie.199306061/abstract | - |
heal.journalName | Angew. Chem. Int. Ed. Engl. | en |
heal.journalType | peer reviewed | - |
heal.language | en | - |
heal.publicationDate | 1993 | - |
heal.publisher | VCH Verlagsgesellschaft | en |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.type | journalArticle | - |
heal.type.el | Άρθρο Περιοδικού | el |
heal.type.en | Journal article | en |
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