Qualitative evaluation of regioselectivity in the formation of di- and tri-6-O-tritylates of α-cyclodextrin.

The quantitative analysis of reaction products showed that the reaction of 6(A),6(D)-di-O-trityl-α-cyclodextrin (CD), AD-isomer, with trityl chloride in pyridine at 55 °C gave 6(A),6(B),6(E)-tri-O-trityl-α-CD, the amount of which was only 25% of that of simultaneously formed 6(A),6(B),6(D)-tri-O-trityl-α-CD. This indicates that the bulky trityl groups of glucopyranose-A and -D (Glu-A and -D, respectively) in the AD-isomer mainly retard the additional tritylation of the C(6)-OH of the adjacent glucopyranoses in a counter-clockwise direction (Glu-F and -C, respectively). (1)H NMR spectra of the AD-isomer showed that the O(6)-H and C(6)-H signals of Glu-C and -F are shifted upfield due to the ring current of the trityl groups.

Regioselectivity in the formation of di- and tri-6-O-mesitylenesulfonates of α-cyclodextrin.

The quantitative analysis of the reaction products for α-cyclodextrin (α-CD) with mesitylenesulfonyl chloride (MessCl) showed that di- and tri-mesitylenesulfonylation of the primary hydroxy groups of α-CD is regioselective. The reaction of mono-6-O-mesitylenesulfonyl-α-CD with MessCl in pyridine gave less 6(A),6(C)-di-O-mesitylenesulfonyl-α-CD than 6(A),6(B)-di-O-mesitylenesulfonyl-α-CD. The reaction of 6(A),6(D)-di-O-mesitylenesulfonyl-α-CD with MessCl gave less 6(A),6(B),6(E)-tri-O-mesitylenesulfonyl-α-CD than 6(A),6(B),6(D)-tri-O-mesitylenesulfonyl-α-CD.

Synthesis and structure-activity relationships of 1-phenyl-1H-1,2,3-triazoles as selective insect GABA receptor antagonists.

To study the interaction of phenylheterocycles with gamma-aminobutyric acid (GABA) receptors, 4- or 5-alkyl(or phenyl)-1-phenyl-1H-1,2,3-triazoles were synthesized and examined for their ability to inhibit the specific binding of [3H]-4'-ethynyl-4-n-propylbicycloorthobenzoate (EBOB), a noncompetitive antagonist, to the housefly and rat GABA receptors, as well as to the beta3 subunit homo-oligomer of the human GABA receptor investigated as a model receptor. 4-Substituted 1-phenyl-1H-1,2,3-triazoles were found to be more potent competitive inhibitors than the 5-substituted regioisomers in the case of all receptors. The 4-tert-butyl or 4-n-propyl analogue of 1-(2,6-dichloro-4-trifluoromethylphenyl)-1H-1,2,3-triazole exhibited the highest level of inhibition of [3H]EBOB binding to all receptors.

Retarding effects of cyclodextrins on the decomposition of organic isothiocyanates in an aqueous solution.

One- and two-dimensional (1)H nuclear magnetic resonance ((1)H NMR) spectra were measured in order to estimate the dissociation constants (K(diss)) and molecular geometries of cyclodextrin (CD) with three organic isothiocyanates (ITC), allyl-ITC, 3-butenyl-ITC, and 4-pentenyl-ITC, in an aqueous solution (pH 5.0, I(c)=0.75 M).

Carboxylations of alkali metal phenoxides with carbon dioxide.

The reaction mechanism of the Kolbe-Schmitt reaction of phenol and 2-naphthol has been investigated. An alkali metal phenoxide-CO2 complex is not an intermediate that can be easily transformed into a carboxylic acid, such as salicylic acid (SA) and p-hydroxybenzoic acid (pHBA). A direct carboxylation of phenoxide with CO2 takes place even at room temperature, and is competitive with the formation of the CO2 complex.