Search Results - "Razumova, N. G."

Reactivity of Inorganic α-Nucleophiles in Acyl Transfer in Aqueous and Micellar Media: IV. Peroxyhydrolysis of Acyl Derivatives in Organized Microheterogeneous Systems1 by Turovskaya, M. K., Belousova, I. A., Razumova, N. G., Gaidash, T. S., Prokop’eva, T. M., Kotenko, A. A., Mikhailov, V. A.

“…The micellar effects in the perhydrolysis and base-catalyzed hydrolysis of 4-nitrophenyl esters of phosphoric, phosphonic, and toluenesulfonic acids in…”
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Reactivity of Inorganic α-Nucleophiles in Acyl Transfer Processes in Water and Surfactant Micelles: III. Systems Based on Dimeric Cationic Imidazolium Surfactants in Alkaline Hydrolysis of Ethyl 4-Nitrophenyl Ethylphosphonate by Belousova, I. A., Zubareva, T. M., Gaidash, T. S., Razumova, N. G., Turovskaya, M. K., Panchenko, B. V., Prokop’eva, T. M., Mikhailov, V. A.

“…The kinetics of alkaline hydrolysis of ethyl 4-nitrophenyl ethylphosphonate in micelles formed by cationic dimeric imidazolium surfactants [AlkIm + (CH 2 ) m…”
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Supernucleophilic Systems Underlain by Functionalized Surfactants in Cleavage of 4-Nitrophenyl Esters of Phosphorus and Sulfur Acids: IV. Micellar Effects of Functionalized Surfactants with a Variable Nature of the Head Group and Hydrophobicity in Transfer Reactions of the Phosphonyl Group by Prokop’eva, T. M., Belousova, I. A., Turovskaya, M. K., Razumova, N. G., Panchenko, B. V., Mikhailov, V. A.

“…[2-(Hydroxyimino)]dimethylalkylammonium bromides (Alk = C 16 H 33 , C 14 H 29 , C 12 H 25 ) were synthesized and their reactivity was investigated in the…”
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Reactivity of Inorganic α-Nucleophiles in Acyl Group Transfer Processes in Water and Surfactant Micelles: II.1 Alkaline Hydrolysis of Ethyl 4-Nitrophenyl Ethylphosphonate in Systems Based on Dimeric Cationic Surfactants by Zubareva, T. M., Belousova, I. A., Prokop’eva, T. M., Gaidash, T. S., Razumova, N. G., Panchenko, B. V., Mikhailov, V. A.

“…Alkaline hydrolysis of ethyl 4-nitrophenyl ethylphosphonate in organized nanosized systems based on dimeric surfactants and co-micelles [with…”
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Reactivity of co-micellar systems based on dimeric functionalized tetraalkylammonium surfactant in phosphoryl and sulfonyl group transfer processes by Prokop’eva, T. M., Kapitanov, I. V., Belousova, I. A., Shumeiko, A. E., Kostrikin, M. L., Serdyuk, A. A., Turovskaya, M. K., Razumova, N. G.

“…The reactivity of co-micellar systems based on dimeric functionalized tetraalkylammonium surfactant in phosphoryl and sulfonyl group transfer processes is…”
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Kinetic regularities of micellar catalysis in the dephosphorylation with peroxide anion by Vakhitova, L. N, Matvienko, K. V, Skrypka, A. V, Taran, N. A, Razumova, N. G, Popov, A. F, Savelova, V. A

“…The acid-base equilibrium of hydrogen peroxide in water solutions of cetyltrimethylammonium bromideand the reactivity of hydroxide and peroxide anions with…”
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Supernucleophilic systems based on functionalized surfactants in the decomposition of 4-nitrophenyl esters derived from phosphorus and sulfur acids. III. Reactivity of mixed micellar systems based on tetraalkylammonium and imidazolium surfactants by Prokop’eva, T. M., Kapitanov, I. V., Belousova, I. A., Shumeiko, A. E., Kostrikin, M. L., Turovskaya, M. K., Razumova, N. G., Popov, A. F.

“…Reactivity of mixed micellar systems based on the functionalized imidazolium and tetraalkylammonium surfactanats in the reaction of cleavage of 4-nitrophenyl…”
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Reactivity of the H2O2/B(OH)3/HO- system in the decomposition of 4-nitrophenyl esters of diethylphosphonic and diethylphosphoric acids by Sadovskii, Yu. S., Solomoichenko, T. N., Prokop’eva, T. M., Piskunova, Zh. P., Razumova, N. G., Panchenko, B. V., Popov, A. F.

“…The kinetics of the decomposition of 4-nitrophenyl diethylphosphonate and 4-nitrophenyl diethyl phosphate by the H 2 O 2 /B(OH) 3 /HO – system with wide…”
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Reactivity of functional detergents with a pyridine ring and an α-nucleophile fragment in the head group by Belousova, I. A., Kapitanov, I. V., Shumeiko, A. E., Mikhailov, V. A., Razumova, N. G., Prokop’eva, T. M., Popov, A. F.

“…Functional detergents (FD) based on pyridine and containing aldoximate, ketoximate, and hydroxamate groups were synthesized. Their reactivity in FD/CTAB…”
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Characteristic features of the change in reactivity of supernucleophilic functional surfactants in acyl group transfer processes by Prokop’eva, T. M., Karpichev, E. A., Belousova, I. A., Turovskaya, M. K., Shumeiko, A. E., Kostrikin, M. L., Razumova, N. G., Kapitanov, I. V., Popov, A. F.

“…We consider the factors responsible for the nucleophilicity and micellar effects of surfactants based on imidazole and pyridine, functionalized by an oximate…”
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Reactivity of micelle-forming 1-alkyl-3(1-oximinoethyl)pyridinium bromides in acyl group transfer reactions by Turovskaya, M. K., Kapitanov, I. V., Belousova, I. A., Tuchinskaya, K. K., Shumeiko, A. E., Kostrikin, M. L., Razumova, N. G., Prokop’eva, T. M., Popov, A. F.

“…The reactivity of a series of micelle-forming 1-alkyl-3-(1-oximinoethyl)pyridinium bromides in the cleavage of typical acyl substrates was studied and…”
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Effect of cetyltrimethylammonium bromide micelles on the ionic equilibrium and the reactivity of hydrogen peroxide toward electrophilic substrates by Vakhitova, L. N., Bogutskaya, K. V., Taran, N. A., Razumova, N. G., Savelova, V. A., Popov, A. F.

“…The acid-base equilibrium of hydrogen peroxide in aqueous solutions of CTAB and the reactivity of the peroxide anion toward 4-nitrophenyl diethylphosphate and…”
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Micellar catalytic effects in the oxidation of methyl phenyl sulfide with hydrogen peroxide and the hydrogen peroxocarbonate anion by Vakhitova, L. N., Zhil’tsova, S. V., Skrypka, A. V., Razumova, N. G., Taran, N. A., Savelova, V. A., Popov, A. F.

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Reactivity of N-alkyl derivatives of hydroxylamine in decomposition of 4-nitrophenyl diethylphosphonate in water and in cetyltrimethylammonium bromide micelles by Zubareva, T. M., Prokop’eva, T. M., Kapitanov, I. V., Belousova, I. A., Razumova, N. G., Popov, A. F.

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