RUS  ENG
Full version
JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2011 Volume 21, Issue 1, Pages 41–43 (Mi mendc2860)

This article is cited in 13 papers

Chemo- and stereocontrolled alkylation of 1,2-disubstituted at the lower rim 1,2-alternate p-tert-butylthiacalix[4]arene

I. I. Stoikov, A. A. Yantemirova, R. V. Nosov, A. R. Julmetov, V. V. Klochkov, I. S. Antipin, A. I. Konovalov

Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation

Abstract: 1,2-Alternate p-tert-butylthiacalix[4]arene bearing at the lower rim 1,2-positioned acetamide fragments reacts with ethyl bromoacetate to give mono-O-alkylation product when Na2CO3 is used as a base and O,O′,N,N′-tetraalkylation one in the case of K2CO3.

Keywords: thiacalix[4]arene; synthesis; conformation; extraction.

Language: English

DOI: 10.1016/j.mencom.2011.01.017



Bibliographic databases:


© Steklov Math. Inst. of RAS, 2026