Abstract
For the first time a series of new cationic amphiphilic p-tert-butylthiacalix[4]arene derivatives adopting 1,3-alternate stereoisomeric form was synthesized by quaternization of several tertiary amines and N-heterocycles. The structure of all products was well-defined using modern physical technics. The influence of calixarene and amine sterical hindrances on reactivity is discussed.
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Burilov, V. A., Ibragimova, R. R., Gafiatullin, B. H., Nugmanov, R. I., Solovieva, S. E., & Antipin, I. S. (2017). Unusual reactivity of aliphatic and aromatic amines with bromoalkyl derivatives of thiacalix[4]arene in 1,3-alternate stereoisomeric form. Macroheterocycles, 10(2), 215–220. https://doi.org/10.6060/mhc170514b
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