Search Results - "Kostrikin, M. L."

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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Synthesis of some electron-rich aryl(hetaryl)oxiranes under phase-transfer and homogeneous conditions by Afon’kin, A. A., Kostrikin, M. L., Shumeiko, A. E., Popov, A. F.

“…Reactions of mono-, di-, and trimethoxybenzaldehydes with trimethylsulfonium methyl sulfate readily occur under mild homogeneous and heterogeneous…”
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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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Supernucleophilic systems based on functionalized surfactants in the decomposition of 4-nitrophenyl esters derived from phosphorus and sulfur acids: II. Influence of the length of hydrophobic alkyl substituents on micellar effects of functionalized monomeric and dimeric imidazolium surfactants by Kapitanov, I. V., Belousova, I. A., Shumeiko, A. E., Kostrikin, M. L., Prokop’eva, T. M., Popov, A. F.

“…New dimeric functionalized surfactants, 3,3′-[2-(hydroxyimino)propan-1,3-diyl]bis(1-alkyl-1 H -imidazol-3-ium) dichlorides (Alk = C 12 H 25 , C 14 H 29 , C 16…”
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6,7-Dimethoxy-3,4-dihydroisoquinolin-1(2H)-ylidenoacetonitrile in some fusion reactions by Afon’kin, A. A., Kostrikin, M. L., Shumeiko, A. E., Popov, A. F.

“…6,7-Dimethoxy-3,4-dihydroisoquinolin-1-ylacetonitrile in the enamine form readily reacts with acyl iso(thio)cyanates affording in high yields 1,2-fused oxo-…”
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Supernucleophilic systems based on functionalized surfactants in the decomposition of 4-nitrophenyl esters derived from phosphorus and sulfur acids: I. Reactivity of a hydroxyimino derivative of gemini imidazolium surfactant by Kapitanov, I. V., Belousova, I. A., Shumeiko, A. E., Kostrikin, M. L., Prokop’eva, T. M., Popov, A. F.

“…A new functionalized gemini surfactant, 3,3′-[2-(hydroxyimino)propane-1,3-diyl]bis(1-dodecyl-1 H -imidazol-3-ium) dichloride, and its non-micelle-forming…”
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Regio- and stereoselective methods for the conversion of (2S,3R)-β-phenylglycidic acid esters to taxoids and other enantiopure (2R,3S)-phenylisoserine esters by Afon’kin, A. A., Kostrikin, L. M., Shumeiko, A. E., Popov, A. F., Matveev, A. A., Matvienko, V. N., Zabudkin, A. F.

“…A novel efficient method was proposed for the synthesis of enantiopure precursors of taxane-containing cytostatics, i.e. , methyl esters of (2 R ,3 S )- and (2…”
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Peroxyhydrolysis of 4-nitrophenyl diethyl phosphate in micellar systems based on imidazolium gemini surfactants by Sadovskii, Yu. S., Solomoichenko, T. N., Turovskaya, M. K., Kapitanov, I. V., Piskunova, Zh. P., Kostrikin, M. L., Prokop’eva, T. M., Popov, A. F.

“…The nucleophilic reactivity of HO – and HOO – ions in the presence of imidazole gemini surfactants toward 4-nitrophenyl diethyl phosphate (NPDEP) was studied…”
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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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Nucleophilicity of functional surface active substances in the transfer of phosphoryl groups by Turovskaya, M. K., Prokop’eva, T. M., Karpichev, E. A., Shumeiko, A. E., Kostrikin, M. L., Savelova, V. A., Kapitanov, I. V., Popov, A. F.

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Regioselectivity in azoles alkylation. Benzylation of indazole under conditions of the phase-transfer catalysis by Shumeiko, A. E., Afon’kin, A. A., Pazumova, N. G., Kostrikin, M. L.

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