Abstract
Thiacalix[4]arenes mono-, 1,3-di-, tri-, and tetrasubstituted at the lower rim, including those containing different substituents, were synthesized by the method based on the ability of the phenacyl moiety to serve as the protecting group, as well as to be involved in transalkylation.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 476–488, March, 2011.
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Solovieva, S.E., Popova, E.V., Omran, A.O. et al. Unusual functionalization of the lower rim of thiacalix[4]arene: competition of alkylation and transalkylation. Russ Chem Bull 60, 486 (2011). https://doi.org/10.1007/s11172-011-0076-0
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DOI: https://doi.org/10.1007/s11172-011-0076-0