Synthesis and chiral recognition properties of two novel chiral calix[4]arene tartaric ester derivatives

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dc.contributor.authorKaraküçük, Ayşegül
dc.contributor.authorDurmaz, Mustafa
dc.contributor.authorSirit, Abdülkadir
dc.contributor.authorYılmaz, Mustafa
dc.contributor.authorDemir, Ayhan S.
dc.date.accessioned2020-03-26T17:04:25Z
dc.date.available2020-03-26T17:04:25Z
dc.date.issued2006
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractTwo new chiral calix[4]arene derivatives containing tartaric acid ester moieties were synthesized. The chiral calix[4]arenes are in a 'cone' conformation according to NMR spectroscopy. The chiral recognition capabilities of 1-4 toward the guests, 1,2-propanediol and serine methyl ester hydrochloride (SerOMe), were investigated (H-1 NMR spectroscopy). The extraction properties of compounds 1 and 2 toward selected alpha-amino acid methyl esters were also studied. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tetasy.2006.07.011en_US
dc.identifier.endpage1968en_US
dc.identifier.issn0957-4166en_US
dc.identifier.issue13en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage1963en_US
dc.identifier.urihttps://dx.doi.org/10.1016/j.tetasy.2006.07.011
dc.identifier.urihttps://hdl.handle.net/20.500.12395/20699
dc.identifier.volume17en_US
dc.identifier.wosWOS:000240242300007en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDen_US
dc.relation.ispartofTETRAHEDRON-ASYMMETRYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.titleSynthesis and chiral recognition properties of two novel chiral calix[4]arene tartaric ester derivativesen_US
dc.typeArticleen_US

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