Enhanced sugar-binding ability of deprotonated calix[4]resorcarene in water: Balance of CH-π interaction and hydrophobic effect
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Complexation of hydrophobic sugars and nucleosides in water with tetrasulfonate derivatives of resorcinol cyclic tetramer having a polyhydroxy aromatic cavity: importance of guest-host CH-.pi. interaction
2. Complexation of methylammonium salts and sugar-related alcohols with resorcinol cyclic tetramer in water: An implication of the CH-π interaction on polar guest binding
3. CH-.pi. interaction as an important driving force of host-guest complexation in apolar organic media. Binding of monools and acetylated compounds to resorcinol cyclic tetramer as studied by proton NMR and circular dichroism spectroscopy
4. Host-guest chemistry. 14. Solvent and salt effects on binding constants of organic substrates in macrocyclic host compounds. A general equation measuring hydrophobic binding contributions
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