Enantioselective Recognition of Amino Acids by Enantiomerically Pure Calix[4]arene Carboxylic Acid or Their Diastereomerically Pure N-(1-Phenyl)ethyl Amides

Elena A. Andreyko,^a Ivan I. Stoikov,^a@ Igor S. Antipin,^a Andrii O. Karpus,^b Anton M. Sikorsky,^b Oleksandr A. Yesypenko,^b Alexander B. Rozhenko,^b Vyacheslav I. Boyko,^b and Vitaly I. Kalchenko^b

^aKazan (Volga Region) Federal University, A. M. Butlerov Chemical Institute, 420008 Kazan, Russian Federation

^bInstitute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev-94, 02660 Ukraine

^@Corresponding author E-mail: ivan.stoikov@mail.ru

DOI: 10.6060/mhc130747s

Macroheterocycles 2013 6(3) 227-233

The interaction of inherently chiral calix[4]arene carboxylic acids and their amides with amino acids in the organic phase has been studied using electron spectroscopy. It was found that the chiral calix[4]arenes are able to enantioselective recognition of L- and D-forms of amino acids.

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