Abstract
Abstract Chiral recognition of chiral amines 4–10 by lipophilic peptide derivatives 1–3 was studied spectrophotometrically in chloroform. Peptide 3 as compared with 2 indicated greater binding affinity and enantiomer selectivity towards the (R)-isomer of 4 and 6. Also 3 showed strikingly high binding and diastereoselectivity towards 9 and 10.
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