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• W2112562509 startingPage "4458" @default.
• W2112562509 abstract "Abstract A straightforward synthesis of C 3 ‐symmetric, imidazole‐containing, macrocyclic peptides with different binding arms is presented. The chirality of the backbone and the selection of adequate receptor arms make these systems highly selective receptors for α‐chiral primary organoammonium ions. Furthermore, the receptors have the ability to discriminate between enantiomeric guests with selectivity ratios of up to 87:13. The binding constants and the selectivity ratios were estimated by standard 1 H NMR titration techniques in CDCl 3 . (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)" @default.
• W2112562509 created "2016-06-24" @default.
• W2112562509 creator A5002324040 @default.
• W2112562509 creator A5045060395 @default.
• W2112562509 date "2009-08-24" @default.
• W2112562509 modified "2023-10-08" @default.
• W2112562509 title "Highly Selective Recognition of α-Chiral Primary Organoammonium Ions by<i>C</i>₃-Symmetric Peptide Receptors" @default.
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• W2112562509 doi "https://doi.org/10.1002/ejoc.200900510" @default.
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