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1,3-Disubstituted p-tert-butylcalix[4]arenes as cholinesterase inhibitors

Enzymatic determination of α-aminophosphonates with butyryl cholinesterase and carboxylesterase in an acidic medium. With the use of carboxylesterase, whose activity hardly depended on the pH of the medium

1,3-Disubstituted p-tert-butylcalix[4]arenes as cholinesterase inhibitors

Enzymatic determination of α-aminophosphonates with butyryl cholinesterase and carboxylesterase in an acidic medium. With the use of carboxylesterase, whose activity hardly depended on the pH of the medium

Influence of the structure of nonionic surfactants and the length of alkyl substituents of calix[4]resorcinarenes on their solubility, acid-base, and complexation propertiesRegularities of solubilization of calix[4]resorcinarenes (H8L) with the variable length

Influence of the structure of nonionic surfactants and the length of alkyl substituents of calix[4]resorcinarenes on their solubility, acid-base, and complexation propertiesRegularities of solubilization of calix[4]resorcinarenes (H8L) with the variable length

Atmospheric and high pressure ene reaction of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in toluene, which is accompanied by Wagner

Ene reaction of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione with dicyclopentadiene-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in benzene, toluene, acetonitrile, 1,2-dichloroetane

pH-driven variation of the outer-sphere binding mode of cis-[Co(Ad)(en)2Cl]Cl (en-ethylendiamine, ad-adeninate) with p-sulfonatothiacalix[4]arene-sulfonatothiacalix[4]arene (STCA) to study the inclusion complex formation at wide range of pH 2-10. It was shown by 1H

Ene Reaction of β-Pinene with 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione: Effects of Temperature, High Pressure, and Solvent Nature pressure on the rate of the ene reaction of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione with β-pinene have

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