Abstract
New amphiphilic benzylated calix[4]resorcinols were synthesized by the reaction of tetra-alkylcalix[4]resorcinols with 3,5-di(tert-butyl)-4-hydroxybenzyl acetate. The reaction pathway and the type of the products formed are determined by the structure of the alkyl substituent at the lower rim of tetraalkylcalix[4]resorcinols and the nature of acid used as a catalyst of the process. Self-organization of some synthesized compounds in nonpolar media was studied.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 138–144, January, 2009.
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Kasymova, E.M., Burilov, A.R., Mukmeneva, N.A. et al. Benzylation of tetraalkylcalix[4]resorcinols. Russ Chem Bull 58, 138–144 (2009). https://doi.org/10.1007/s11172-009-0021-7
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DOI: https://doi.org/10.1007/s11172-009-0021-7