p-tert-Butyl Thiacalix[4]arene Derivatives Functionalized in the Lower Rim with Bis(3-aminopropyl)amine: Synthesis and Interaction with DNA

Joshua B. Puplampu,^a Luidmila S. Yakimova,^a Alena A. Vavilova,^a Ildar Kh. Rizvanov,^b and Ivan I. Stoikov^a^@

^aKazan Federal University, A.M. Butlerov Chemical Institute, 420008, Kremlevskaya Street, 18, Kazan, Russian Federation.

^bA.E. Arbuzov’ Institute of Organic and Physical Chemistry of KSC RAS, 420088, Acad. Arbuzov 8, Kazan, Russian Federation

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

DOI: 10.6060/mhc140722s

Macroheterocycles 2015 8(1) 75-80

New tetrasubstituted derivatives of thiacalix[4]arene functionalized with bis(3-aminopropyl)amide fragments at the lower rim in the cone and 1,3-alternate conformations have been synthesized. It was demonstrated that the synthesized thiacalix[4]arenes derivatives interact with DNA resulting in a shift in absorption maxima to 257 nm with clear isosbestic point at 300 nm.

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p-tert-Butyl Thiacalix[4]arene Derivatives Functionalized in the Lower Rim with Bis(3-aminopropyl)amine: Synthesis and Interaction with DNA

References: