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dc.contributor.authorFilippova, Liudmila
dc.contributor.authorStenstrøm, Yngve H.
dc.contributor.authorHansen, Trond Vidar
dc.date.accessioned2015-07-28T09:03:02Z
dc.date.accessioned2015-08-17T07:37:27Z
dc.date.available2015-07-28T09:03:02Z
dc.date.available2015-08-17T07:37:27Z
dc.date.issued2015
dc.identifier.citationMolecules 2015, 20:6224-6236nb_NO
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/11250/297114
dc.description-nb_NO
dc.description.abstractA novel C1-symmetric dinitrogen ligand was synthesized in high yield from commercially available (1R,2R,3R,5S)-(−)-isopinocampheylamine and 1-methyl-2- imidazolecarboxaldehyde. In combination with Cu(OAc)2∙H2O, this new ligand promote the reaction between nitromethane and aliphatic aldehydes with high yields (up to 97%) and moderate enantioselectivities (up to 67% ee). The reactions with benzaldehyde required prolonged reaction time that resulted in diminished yields, but accompanied with ee-values in the 55%–76% range.nb_NO
dc.language.isoengnb_NO
dc.relation.urihttp://www.mdpi.com/1420-3049/20/4/6224
dc.rightsNavngivelse 3.0 Norge*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/no/*
dc.titleCu (II)-Catalyzed Asymmetric Henry Reaction with a Novel C1-Symmetric Aminopinane-Derived Ligandnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.date.updated2015-07-28T09:03:02Z
dc.identifier.doi10.3390/molecules20046224
dc.identifier.cristin1237188


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