Synthesis of novel chiral C2-symmetric diaza-18-crown-6 ether derivatives and their enantioselective recognition of amino acid derivatives

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dc.contributor.authorTurgut, Y
dc.contributor.authorDemirel, N
dc.contributor.authorHosgören, H
dc.date.accessioned2024-04-24T16:02:13Z
dc.date.available2024-04-24T16:02:13Z
dc.date.issued2006
dc.departmentDicle Üniversitesien_US
dc.description.abstractNew chiral diaza-18-crown-6 ether derivatives, 5 and 6 were synthesized from (R)-(-)-2-amino-1-butanol. These chiral artificial receptors exhibit pronounced chiral recognition toward the enantiomers of L- and D- amino acid derivatives. The highest enantioselectivity was observed in the case of Trp-OMe center dot HCl (K-D/ K-L= 12.5).en_US
dc.identifier.doi10.1007/s10847-005-3125-1
dc.identifier.endpage33en_US
dc.identifier.issn1388-3127
dc.identifier.issn1573-1111
dc.identifier.issue1-2en_US
dc.identifier.scopus2-s2.0-29144437208
dc.identifier.scopusqualityQ2
dc.identifier.startpage29en_US
dc.identifier.urihttps://doi.org/10.1007/s10847-005-3125-1
dc.identifier.urihttps://hdl.handle.net/11468/14694
dc.identifier.volume54en_US
dc.identifier.wosWOS:000233876700005
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofJournal of Inclusion Phenomena and Macrocyclic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmino Aciden_US
dc.subjectChiral Aza Crown Etheren_US
dc.subjectComplexationen_US
dc.subjectMolecular Recognitionen_US
dc.titleSynthesis of novel chiral C2-symmetric diaza-18-crown-6 ether derivatives and their enantioselective recognition of amino acid derivativesen_US
dc.titleSynthesis of novel chiral C2-symmetric diaza-18-crown-6 ether derivatives and their enantioselective recognition of amino acid derivatives
dc.typeArticleen_US

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