Synthesis of new chiral crown ethers containing a (p-methoxyphenoxy)methyl moiety and their chiral recognition ability towards amino acid esters

dc.contributor.authorKarakaplan, M
dc.contributor.authorAral, T
dc.date.accessioned2024-04-24T16:18:26Z
dc.date.available2024-04-24T16:18:26Z
dc.date.issued2005
dc.departmentDicle Üniversitesien_US
dc.description.abstractNovel crown ethers 9-13 containing a chiral subunit derived from 3-(p-methoxyphenoxy)propane-1,2-diol 7 were prepared in enantiomerically pure forms. Chiral recognition properties of these receptors towards L- and D-amino acid derivatives were examined by the UV-vis titration method. These receptors exhibit good chiral recognition towards the isomers (up to K-1/J(p) = 5.81, Delta Delta G(0) = 4.30 kJ mol(-1)) in CHCl3 at 25 degrees C. (c) 2005 Published by Elsevier Ltd.en_US
dc.identifier.doi10.1016/j.tetasy.2005.05.019
dc.identifier.endpage2124en_US
dc.identifier.issn0957-4166
dc.identifier.issue12en_US
dc.identifier.scopus2-s2.0-20444382752
dc.identifier.scopusqualityN/A
dc.identifier.startpage2119en_US
dc.identifier.urihttps://doi.org/10.1016/j.tetasy.2005.05.019
dc.identifier.urihttps://hdl.handle.net/11468/16096
dc.identifier.volume16en_US
dc.identifier.wosWOS:000230186600011
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedron-Asymmetry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleSynthesis of new chiral crown ethers containing a (p-methoxyphenoxy)methyl moiety and their chiral recognition ability towards amino acid estersen_US
dc.titleSynthesis of new chiral crown ethers containing a (p-methoxyphenoxy)methyl moiety and their chiral recognition ability towards amino acid esters
dc.typeArticleen_US

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