845822-75-5Relevant academic research and scientific papers
Synthetic receptors based on calix[4]arene functionalized at the lower rim in molecular recognition of dicarboxylic, α-hydroxycarboxylic, and α-amino acids
Stoikov,Gafiullina,Ibragimova,Antipin,Konovalov
, p. 1172 - 1180 (2004)
New calix[4]arenes, di- and tetrasubstituted at the lower rim, with different functional groups were synthesized. They were studied as carriers of a series of dicarboxylic and α-hydroxycarboxylic acids through a liquid impregnated membrane. The calix[4]arenes under study are capable of molecular recognition of oxalic acid in the series of structurally similar dicarboxylic and α-hydroxycarboxylic acids. The regularities found make it possible to change purposefully the receptor ability of 1,3-disubstituted calix[4]arenes by variation of the nature of substituents.
Choline esterase inhibitors and synthetic oxalic acid receptors based on calix[4]arene derivatives
Stoikov,Khrustalev,Ibragimova,Stoikova,Evtyugin,Antipin,Konovalov
, p. 278 - 284 (2007/10/03)
New reversible butyrylcholine esterase inhibitors based on calix[4]arene derivatives were suggested. A series of new distally disubstituted calix[4]arenes were prepared in 60-80% yields. Some of these compounds showed properties of reversible choline este
