Mono-, 1,3-Di- and Tetrasubstituted p-tert-Butylthiacalix[4]arenes Containing Phthalimide Groups: Synthesis and Functionalization with Ester, Amide, Hydrazide and Amino Groups

Andrey V. Galukhin,^a Evgeny N. Zaikov,^a Igor S. Antipin,^a Alexander I. Konovalov,^a and Ivan I. Stoikov^a,b@

^aKazan (Volga Region) Federal University, A.M.Butlerov Chemical Institute, 420008 Kazan, Russian Federation
^bKazan Institute of Biochemistry and Biophysics, Russian Academy of Sciences, 420111 Kazan, Russian Federation.

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

Macroheterocycles 2012 5(3) 266-274

DOI: 10.6060/mhc2012.120781s

The introduction of the phthalimide group in the p-tert-butylthiacalix[4]arenes tetrasubstituted at the lower rim with ester and amide groups significantly influences the selectivity of the extraction of the alkali metal cations.

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