Karaküçük, AyşegülDurmaz, MustafaSirit, AbdülkadirYılmaz, MustafaDemir, Ayhan S.2020-03-262020-03-2620060957-4166https://dx.doi.org/10.1016/j.tetasy.2006.07.011https://hdl.handle.net/20.500.12395/20699Two 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.en10.1016/j.tetasy.2006.07.011info:eu-repo/semantics/closedAccessSynthesis and chiral recognition properties of two novel chiral calix[4]arene tartaric ester derivativesArticle171319631968N/AWOS:000240242300007Q2