Search Results - "Turovskaya, M. K."

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  1. 1

    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.

    Published in Russian journal of organic chemistry (01-02-2024)
    “…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 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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    Reactivity of micellar systems based on supernucleophilic functional surfactants in processes of acyl group transfer by Kapitanov, I. V., Belousova, I. A., Turovskaya, M. K., Karpichev, E. A., Prokop’eva, T. M., Popov, A. F.

    Published in Russian journal of organic chemistry (01-05-2012)
    “…Processes of cleavage of 4-nitrophenyl esters of diethylphosphoric, diethylphosphonic, and 4-toluenesulfonic acids were investigated occurring in micelles of…”
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  8. 8

    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.

    Published in Theoretical and experimental chemistry (01-05-2012)
    “…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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  9. 9

    New sources of “active” halogen bis(dialkylamide)hydrogen dibromobromates, efficient reagents for destruction of ecotoxicants by Prokop’eva, T. M., Mikhailov, V. A., Turovskaya, M. K., Karpichev, E. A., Burakov, N. I., Savelova, V. A., Kapitanov, I. V., Popov, A. F.

    Published in Russian journal of organic chemistry (01-05-2008)
    “…Bis(dialkylamide)hydrogen dibromobromates were synthesized and their reactivity was investigated in decomposition of diethylphosphonic, diethylphosphoric, and…”
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  10. 10

    Role of the hydrophobic properties of functional detergents on micellar effects in the dissociation of environmental toxicants by Belousova, I. A., Kapitanov, I. V., Shumeiko, A. E., Anikeev, A. V., Turovskaya, M. K., Zubareva, T. M., Panchenko, B. V., Prokop’eva, T. M., Popov, A. F.

    Published in Theoretical and experimental chemistry (01-11-2010)
    “…1-Alkyl-3-(2-oximinopropyl)imidazolium chlorides were prepared with different alkyl chain lengths (Alk = C 12 H 25 , C 14 H 29 ). Some physicochemical indices…”
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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.

    Published in Theoretical and experimental chemistry (01-07-2010)
    “…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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  12. 12

    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.

    Published in Theoretical and experimental chemistry (01-03-2011)
    “…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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  13. 13

    Structure of the head group, nucleophilicity, and micellar effects of functional detergents in acyl transfer reactions by Belousova, I. A., Kapitanov, I. V., Shumeiko, A. E., Turovskaya, M. K., Prokop’eva, T. M., Popov, A. F.

    Published in Theoretical and experimental chemistry (01-04-2008)
    “…The micellar effects of 1-cetyl-2-methyl-3-(2-hydroxyiminopropyl)imidazolium and 1-cetyl-3-hydroxyiminomethylpyridinium halides in acyl transfer reactions…”
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    Bis(dialkylamide)hydrogen Dibromobromate Precursors of Hypobromite Ion in Reactions with Nerve and Blister Agent Simulants by Simanenko, Yuri S, Savelova, Vera A, Prokop'eva, Tatyana M, Mikhailov, Vasily A, Turovskaya, Marya K, Karpichev, Eugen A, Popov, Anatolii F, Gillitt, Nicholas D, Bunton, Clifford A

    Published in Journal of organic chemistry (24-12-2004)
    “…Hypobromite ion, BrO-, is an effective α-nucleophile that reacts rapidly with activated phosphorus(V) and sulfonate esters. The parent acid rapidly oxidizes…”
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    Journal Article