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Volumn 9, Issue 3-4, 2010, Pages 337-353

New insights into detoxification of chemical warfare simulants and pesticides using micelle mediated systems

Author keywords

Decontamination; Detoxification; Functionalized surfactants; Nerve agents; Organophosphate; Oxime reactivators; Pesticides

Indexed keywords


EID: 78650648200     PISSN: 10241221     EISSN: 17451167     Source Type: Journal    
DOI: 10.3233/MGC-2010-0026     Document Type: Conference Paper
Times cited : (4)

References (64)
  • 2
    • 52449129804 scopus 로고    scopus 로고
    • Hydroxylamine as an oxygen nucleophile: Chemical evidence from its reaction with a phosphate trimester
    • A.J. Kirby, B.S. Souza,M.Medeiros, J.P. Priebe, A.M.Manfredi and F. Nome, Hydroxylamine as an oxygen nucleophile: Chemical evidence from its reaction with a phosphate trimester, Chem Commun (2008), 4428.
    • (2008) Chem Commun , pp. 4428
    • Kirby, A.J.1    Souza, B.S.2    Medeiros, M.3    Priebe, J.P.4    Manfredi, A.M.5    Nome, F.6
  • 4
    • 35349018354 scopus 로고    scopus 로고
    • Unequal Efficacy of Pyridinium oximes in acute organophosphate poisoning
    • B. Antonijevic and M.P. Stojilkovic, Unequal Efficacy of Pyridinium oximes in acute organophosphate poisoning, Clin Med Res 5 (2007), 71.
    • (2007) Clin Med Res , vol.5 , pp. 71
    • Antonijevic, B.1    Stojilkovic, M.P.2
  • 5
    • 35348874818 scopus 로고    scopus 로고
    • Evaluation of HI6 oxime: Potential use in protection of human acetylcholinesterase inhibited by antineoplastic drug irinotecan and its cyto/genotoxicity in vitro
    • B. Radic, A.L. Vrdoljak, D. Zelezic, N. Fuchs, S. Berend and M. Kopjar, Evaluation of HI6 oxime: potential use in protection of human acetylcholinesterase inhibited by antineoplastic drug irinotecan and its cyto/genotoxicity in vitro, Acta Biochim Polon 54 (2007), 583.
    • (2007) Acta Biochim Polon , vol.54 , pp. 583
    • Radic, B.1    Vrdoljak, A.L.2    Zelezic, D.3    Fuchs, N.4    Berend, S.5    Kopjar, M.6
  • 6
    • 38549163108 scopus 로고    scopus 로고
    • Catalytic methods for the destruction of chemical warfare agents under ambient conditions
    • B.M. Smith, Catalytic methods for the destruction of chemical warfare agents under ambient conditions, Chem Soc Rev 3 (2008), 470.
    • (2008) Chem Soc Rev , vol.3 , pp. 470
    • Smith, B.M.1
  • 7
    • 0032482901 scopus 로고    scopus 로고
    • A Quantitative treatment of dephosphorylation by an amphiphilic hydroxamate Ion: The role of micellar charge
    • C.A. Bunton, N.D. Gillitt and H.J. Foroudian, A Quantitative treatment of dephosphorylation by an amphiphilic hydroxamate Ion: The role of micellar charge, Langmuir 14 (1998), 4415.
    • (1998) Langmuir , vol.14 , pp. 4415
    • Bunton, C.A.1    Gillitt, N.D.2    Foroudian, H.J.3
  • 8
    • 0037168749 scopus 로고    scopus 로고
    • Micellar effects on hypochlorite catalyzed decontamination of toxic phosphorus esters
    • D.K. Dubey, A.K. Gupta, M. Sharma, S. Prabha and R. Vaidyanathaswami, Micellar effects on hypochlorite catalyzed decontamination of toxic phosphorus esters, Langmuir 18 (2002), 10489.
    • (2002) Langmuir , vol.18 , pp. 10489
    • Dubey, D.K.1    Gupta, A.K.2    Sharma, M.3    Prabha, S.4    Vaidyanathaswami, R.5
  • 9
    • 50649098272 scopus 로고    scopus 로고
    • Potency of several oximes to reactivate human acetylcholinesterase and butyrylcholinesterase inhibited by paraoxon and methylparaoxon in vitro
    • D. Jun, L.Musilova, K. Kuca, J. Kassa and J. Bajgar, Potency of several oximes to reactivate human acetylcholinesterase and butyrylcholinesterase inhibited by paraoxon and methylparaoxon in vitro, Chem Biol Interact 175 (2008), 421.
    • (2008) Chem Biol Interact , vol.175 , pp. 421
    • Jun, D.1    Musilova, L.2    Kuca, K.3    Kassa, J.4    Bajgar, J.5
  • 10
    • 0037205895 scopus 로고    scopus 로고
    • Reactions of Oximate anucleophiles with esters: Evidence from solvation effects for substantial decoupling of desolvation and bond formation
    • E. Buncel, C. Cannes, A.P. Chatrousse and F. Terrier, Reactions of Oximate anucleophiles with esters: Evidence from solvation effects for substantial decoupling of desolvation and bond formation, J Am Chem Soc 124 (2002), 8766.
    • (2002) J Am Chem Soc , vol.124 , pp. 8766
    • Buncel, E.1    Cannes, C.2    Chatrousse, A.P.3    Terrier, F.4
  • 12
    • 0041837370 scopus 로고    scopus 로고
    • Reactions of bis( 2,4dinitrophenyl) phosphate with hydroxylamine
    • F. Nome, J.B. Domingos, E. Longhinotti and C.A. Bunton, Reactions of bis(2,4dinitrophenyl) phosphate with hydroxylamine, J Org Chem 68 (2003), 7051.
    • (2003) J Org Chem , vol.68 , pp. 7051
    • Nome, F.1    Domingos, J.B.2    Longhinotti, E.3    Bunton, C.A.4
  • 13
    • 0037423974 scopus 로고    scopus 로고
    • The levelling effect of solvational imbalances in the reactions of oximate-nucleophiles with electrophilic phosphorus centers. Relevance to detoxification of organophosphorus esters
    • F. Terrier, E.L. Guevel, A.P. Chatrousse, G. Moutiers and E. Buncel, The levelling effect of solvational imbalances in the reactions of oximate-nucleophiles with electrophilic phosphorus centers. Relevance to detoxification of organophosphorus esters, Chem Commun (2003), 600.
    • (2003) Chem Commun , pp. 600
    • Terrier, F.1    Guevel, E.L.2    Chatrousse, A.P.3    Moutiers, G.4    Buncel, E.5
  • 14
    • 7444221716 scopus 로고    scopus 로고
    • Kinetic analysis of interactions between human acetylcholinesterase structurally different organophosphorus compounds and oximes
    • F. Worek, H. Thiermann, L. Szinicz and P. Eyer, Kinetic analysis of interactions between human acetylcholinesterase, structurally different organophosphorus compounds and oximes, Biochem Pharmacol 68 (2004), 2237.
    • (2004) Biochem Pharmacol , vol.68 , pp. 2237
    • Worek, F.1    Thiermann, H.2    Szinicz, L.3    Eyer, P.4
  • 15
    • 33746303390 scopus 로고
    • Size vs. reactivity in organized assemblies: Deacylation and dephosphorylation in functionalized assemblies
    • G. Biresaw and C.A. Bunton, Size vs. reactivity in organized assemblies: deacylation and dephosphorylation in functionalized assemblies, J Phys Chem 90 (1986), 5849.
    • (1986) J Phys Chem , vol.90 , pp. 5849
    • Biresaw, G.1    Bunton, C.A.2
  • 16
    • 33947611114 scopus 로고    scopus 로고
    • In vitro oxime reactivation of red blood cell acetylcholinesterase inhibitied by methylparaoxon
    • G.A. Petroianu, K. Arafat, S.M. Nurulain, K. Kuca and J. Kassa, In vitro oxime reactivation of red blood cell acetylcholinesterase inhibitied by methylparaoxon, J App Toxicol 27 (2007), 168.
    • (2007) J App Toxicol , vol.27 , pp. 168
    • Petroianu, G.A.1    Arafat, K.2    Nurulain, S.M.3    Kuca, K.4    Kassa, J.5
  • 18
    • 78650643981 scopus 로고    scopus 로고
    • Amphiphilic quaternary pyridinium ketoximes as functional hydrolytic micellar catalysisdoes the nucleophilic function position influence their reactivity?
    • H. Kotoucova, R. Cibulka, F. Hampl and F. Liska, Amphiphilic quaternary pyridinium ketoximes as functional hydrolytic micellar catalysisdoes the nucleophilic function position influence their reactivity? J Mol Catal 3192 (2001), 1.
    • (2001) J Mol Catal , vol.3192 , pp. 1
    • Kotoucova, H.1    Cibulka, R.2    Hampl, F.3    Liska, F.4
  • 19
    • 0035854316 scopus 로고    scopus 로고
    • Solvent effect on the-Effect for the reactions of aryl acetates with butane2,3dione monoximate and pchlorophenoxide in MeCNH2O mixtures
    • I.H. Um, E.J. Lee and E. Buncel, Solvent effect on the-Effect for the reactions of aryl acetates with butane2,3dione monoximate and pchlorophenoxide in MeCNH2O mixtures, J Org Chem 66 (2001), 4859.
    • (2001) J Org Chem , vol.66 , pp. 4859
    • Um, I.H.1    Lee, E.J.2    Buncel, E.3
  • 20
    • 2442645211 scopus 로고    scopus 로고
    • Effects of amine nature and nonleaving group substituents on rate and mechanism in aminolyses of 2,4dinitrophenyl Xsubstituted benzoates
    • I.H. Um, K.H. Kim, H.R. Park, M. Fujio and J. Tsuno, Effects of amine nature and nonleaving group substituents on rate and mechanism in aminolyses of 2,4dinitrophenyl Xsubstituted benzoates, J Org Chem 69 (2004), 3937.
    • (2004) J Org Chem , vol.69 , pp. 3937
    • Um, I.H.1    Kim, K.H.2    Park, H.R.3    Fujio, M.4    Tsuno, J.5
  • 21
    • 0000299571 scopus 로고
    • Micellar acceleration of organophosphate hydrolysis by hydroximinomethylpyridinium type surfactants
    • J. Epstein, J.J. Kaminiski, N. Bodar, R. Eneves, J. Sowa and T. Higuchi, Micellar acceleration of organophosphate hydrolysis by hydroximinomethylpyridinium type surfactants, J Org Chem 43 (1978), 2816.
    • (1978) J Org Chem , vol.43 , pp. 2816
    • Epstein, J.1    Kaminiski, J.J.2    Bodar, N.3    Eneves, R.4    Sowa, J.5    Higuchi, T.6
  • 22
    • 0036447187 scopus 로고    scopus 로고
    • Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents
    • J. Kassa, Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents, J Toxicol Clin Toxicol 40 (2002), 803.
    • (2002) J Toxicol Clin Toxicol , vol.40 , pp. 803
    • Kassa, J.1
  • 23
    • 8644254244 scopus 로고    scopus 로고
    • Reaction of bis 2,4dinitrophenyl) phosphate with hydrazine and hydrogen peroxide: Comparison of oand nphosphorylation
    • J.B. Domingos, E. Longhinotti, T.A.S. Brandao, L.S. Santos, M.N. Eberlin, C.A. Bunton and F. Nome, Reaction of bis (2,4dinitrophenyl) phosphate with hydrazine and hydrogen peroxide: comparison of oand nphosphorylation, J Org Chem 69 (2004), 7898.
    • (2004) J Org Chem , vol.69 , pp. 7898
    • Domingos, J.B.1    Longhinotti, E.2    Brandao, T.A.S.3    Santos, L.S.4    Eberlin, M.N.5    Bunton, C.A.6    Nome, F.7
  • 24
    • 33748654623 scopus 로고    scopus 로고
    • The reactivating and therapeutic efficacy of oximes to counteract russian VX poisonings
    • J. Kassa, D. Jun and K. Kuca, The reactivating and therapeutic efficacy of oximes to counteract russian VX poisonings, Int J Toxicol 25 (2006), 397.
    • (2006) Int J Toxicol , vol.25 , pp. 397
    • Kassa, J.1    Jun, D.2    Kuca, K.3
  • 25
    • 33748444160 scopus 로고    scopus 로고
    • A comparison of the efficacy of new asymmetric bispyridinium oximes (K027, K048) with currently available oximes against tabun by in vivo methods
    • J. Kassa, K. Kuca, J. Cabal and M. Paar, A comparison of the efficacy of new asymmetric bispyridinium oximes (K027, K048) with currently available oximes against tabun by in vivo methods, J Toxicol Environ Health 69 (2006), 1875.
    • (2006) J Toxicol Environ Health , vol.69 , pp. 1875
    • Kassa, J.1    Kuca, K.2    Cabal, J.3    Paar, M.4
  • 26
    • 33947398730 scopus 로고    scopus 로고
    • Oximeinduced reactivation of sarin - Inhibited AChE: A theoretical mechanisms study
    • J. Wang, J. Gu, J. Leszynski, M. Feliks and W. Andrzej, Oximeinduced reactivation of sarin - inhibited AChE: A theoretical mechanisms study, J Phys Chem 111 (2007), 2404.
    • (2007) J Phys Chem , vol.111 , pp. 2404
    • Wang, J.1    Gu, J.2    Leszynski, J.3    Feliks, M.4    Andrzej, W.5
  • 27
    • 38549145987 scopus 로고    scopus 로고
    • In vitro reactivation of sarin inhibited electric eel acetylcholinesterase by bispyridinium oximes bearing methoxy ether linkages
    • J. Acharya, A.K. Gupta, A. Mazumder and D.K. Dubey, In vitro reactivation of sarin inhibited electric eel acetylcholinesterase by bispyridinium oximes bearing methoxy ether linkages, Toxicol In Vitro 22 (2008), 525.
    • (2008) Toxicol in Vitro , vol.22 , pp. 525
    • Acharya, J.1    Gupta, A.K.2    Mazumder, A.3    Dubey, D.K.4
  • 28
    • 0032886037 scopus 로고    scopus 로고
    • The alphaeffect in benzyl transfers from benzylphenylmethyl sulfonium salts to nmethylbenzohydroxamate anions
    • K.R. Fountain, D.B. Tady, T.W. Paul and M.V. Golynskiy, The alphaeffect in benzyl transfers from benzylphenylmethyl sulfonium salts to nmethylbenzohydroxamate anions, J Org Chem 64 (1999), 6547.
    • (1999) J Org Chem , vol.64 , pp. 6547
    • Fountain, K.R.1    Tady, D.B.2    Paul, T.W.3    Golynskiy, M.V.4
  • 29
    • 0037424403 scopus 로고    scopus 로고
    • The alphaeffect in methyl transfers from smethyldibenzothiophenium fluoroborate to substituted nmethylbenzohydroxamates
    • K.R. Fountain, C.J. Felkerson, J.D. Driskell and B.D. Lamp, The alphaeffect in methyl transfers from smethyldibenzothiophenium fluoroborate to substituted nmethylbenzohydroxamates, J Org Chem 68 (2003), 1810.
    • (2003) J Org Chem , vol.68 , pp. 1810
    • Fountain, K.R.1    Felkerson, C.J.2    Driskell, J.D.3    Lamp, B.D.4
  • 30
    • 17744420458 scopus 로고    scopus 로고
    • A comparison of the efficacy of a bispyridinium oxime - 1,4bis( 2hydroxyiminomethylpyridinium) 4( 4carbamoylpyridinium) butane dibromide and currently used oximes to reactivate nerve agentinhibited rat brain acetylcholinesterase by in vitro methods
    • K. Kuca and J. Kassa, A comparison of the efficacy of a bispyridinium oxime - 1,4bis( 2hydroxyiminomethylpyridinium) 4( 4carbamoylpyridinium) butane dibromide and currently used oximes to reactivate nerve agentinhibited rat brain acetylcholinesterase by in vitro methods, J Enzyme Inhib Med Chem 18 (2003), 529.
    • (2003) J Enzyme Inhib Med Chem , vol.18 , pp. 529
    • Kuca, K.1    Kassa, J.2
  • 31
    • 0037424754 scopus 로고    scopus 로고
    • Synthesis of a potential reactivator of acetylcholinesterase 1( 4hydroxyiminomethylpyridinium) 3( carbamoylpyridinium)propane dibromide
    • K. Kuca, J. Bielavsky, J. Cabal and M. Bielavska, Synthesis of a potential reactivator of acetylcholinesterase 1( 4hydroxyiminomethylpyridinium) 3( carbamoylpyridinium)propane dibromide, Tetrahedron Lett 44 (2003), 3123.
    • (2003) Tetrahedron Lett , vol.44 , pp. 3123
    • Kuca, K.1    Bielavsky, J.2    Cabal, J.3    Bielavska, M.4
  • 32
    • 15844422691 scopus 로고    scopus 로고
    • Reactivation of organophosphateinhibited acetylcholinesterase by quaternary pyridinium aldoximes
    • K. Kuca, J. Patocka, J. Cabal and J. Jun, Reactivation of organophosphateinhibited acetylcholinesterase by quaternary pyridinium aldoximes, Neurotoxic Rea 6 (2004), 565.
    • (2004) Neurotoxic Rea , vol.6 , pp. 565
    • Kuca, K.1    Patocka, J.2    Cabal, J.3    Jun, J.4
  • 34
    • 25844496231 scopus 로고    scopus 로고
    • Nucleophilic dephosphorylation of pnitrophenyl diphenyl phosphate in cationic micellar media
    • K.K. Ghosh, D. Sinha, M.L. Satnami, D. Dubey, P.R. Dafonte and G.L. Mundhara, Nucleophilic dephosphorylation of pnitrophenyl diphenyl phosphate in cationic micellar media, Langmuir 21 (2005), 8664.
    • (2005) Langmuir , vol.21 , pp. 8664
    • Ghosh, K.K.1    Sinha, D.2    Satnami, M.L.3    Dubey, D.4    Dafonte, P.R.5    Mundhara, G.L.6
  • 35
    • 33645165150 scopus 로고    scopus 로고
    • The effect in micelles: Nucleophilic substitution reaction of pnitrophenyl acetate with nphenylbenzohydroxamate ion
    • K.K. Ghosh, J. Vaidya and M.L. Satnami, The-effect in micelles: Nucleophilic substitution reaction of pnitrophenyl acetate with nphenylbenzohydroxamate ion, Int J Chem Kinet 38 (2006), 26.
    • (2006) Int J Chem Kinet , vol.38 , pp. 26
    • Ghosh, K.K.1    Vaidya, J.2    Satnami, M.L.3
  • 37
    • 34249731938 scopus 로고    scopus 로고
    • In vitro reactivation potency of acetylcholinesterase reactivators - K074 and K075 - To reactivate tabun inhibited human brain cholinesterases
    • K. Kuca, J. Cabal, D. Jun and K. Musilek, In vitro reactivation potency of acetylcholinesterase reactivators - K074 and K075 - to reactivate tabun inhibited human brain cholinesterases, Neurooxict Res 11 (2007), 101.
    • (2007) Neurooxict Res , vol.11 , pp. 101
    • Kuca, K.1    Cabal, J.2    Jun, D.3    Musilek, K.4
  • 39
    • 34548524594 scopus 로고    scopus 로고
    • Monooxime reactivators of acetylcholinesterase with (E)but2ene linker - Preparation and reactivation of tabunand paraoxoninhibited acetylcholinesterase
    • K. Musilek, O. Holas, D. Jun, V. Dohnal, F. GunnMoore, V. Opletalova, M. Dolezal and K. Kuca, Monooxime reactivators of acetylcholinesterase with (E)but2ene linker - Preparation and reactivation of tabunand paraoxoninhibited acetylcholinesterase, Biorg & Med Chem 15 (2007), 6733.
    • (2007) Biorg & Med Chem , vol.15 , pp. 6733
    • Musilek, K.1    Holas, O.2    Jun, D.3    Dohnal, V.4    Gunn Moore, F.5    Opletalova, V.6    Dolezal, M.7    Kuca, K.8
  • 40
    • 33847301487 scopus 로고    scopus 로고
    • Technological advancements for the detection of and protection against biological and chemical warfare agents
    • L.M. Eubanks, T.J. Dickerson and K.D. Janda, Technological advancements for the detection of and protection against biological and chemical warfare agents, Chem Soc Rev 36 (2007), 458.
    • (2007) Chem Soc Rev , vol.36 , pp. 458
    • Eubanks, L.M.1    Dickerson, T.J.2    Janda, K.D.3
  • 41
    • 42449130611 scopus 로고    scopus 로고
    • Detection of degradation products of chemical warfare agents by highly porous molecularly imprinted microspheres
    • L. Malosse, P. Buvat, D. Ades and A. Siove, Detection of degradation products of chemical warfare agents by highly porous molecularly imprinted microspheres, Analyst 133 (2008), 588.
    • (2008) Analyst , vol.133 , pp. 588
    • Malosse, L.1    Buvat, P.2    Ades, D.3    Siove, A.4
  • 42
    • 63449083967 scopus 로고    scopus 로고
    • Suitability of human butyrylcholinesterase as therapeutic marker and pseudo catalytic scavenger in organophosphate poisoning: A kinetic analysis
    • N. Aurbek, H. Theirmann, F. Eyer, P. Eyer and F.Worek, Suitability of human butyrylcholinesterase as therapeutic marker and pseudo catalytic scavenger in organophosphate poisoning: A kinetic analysis, Toxicology 259 (2009), 133.
    • (2009) Toxicology , vol.259 , pp. 133
    • Aurbek, N.1    Theirmann, H.2    Eyer, F.3    Eyer, P.4    Worek, F.5
  • 43
    • 0000605095 scopus 로고    scopus 로고
    • Anticholinergic agents
    • J.G. Hardman and L.E. Limbird, eds McGraw Hill: New York
    • P. Taylor, Anticholinergic agents, in: The Pharmacological Basis of Therapeutics, J.G. Hardman and L.E. Limbird, eds, McGraw Hill: New York, 1996, pp. 161-176.
    • (1996) The Pharmacological Basis of Therapeutics , pp. 161-176
    • Taylor, P.1
  • 44
    • 84961980140 scopus 로고    scopus 로고
    • Computational study on hydroxybenzotriazoles as reagents for ester hydrolysis
    • P.V. Kumar, B. Ganguly and S. Bhattacharya, Computational study on hydroxybenzotriazoles as reagents for ester hydrolysis, J Org Chem 69 (2004), 8634.
    • (2004) J Org Chem , vol.69 , pp. 8634
    • Kumar, P.V.1    Ganguly, B.2    Bhattacharya, S.3
  • 45
    • 0015350930 scopus 로고
    • Acetylcholinesterase reactivators. Pyridyl and anilyl trifluoromethyl ketoximes
    • R.L. Salvador, M. Saucier, D. Simon and R. Goyer, Acetylcholinesterase reactivators. Pyridyl and anilyl trifluoromethyl ketoximes, J Med Chem 15 (1972), 646.
    • (1972) J Med Chem , vol.15 , pp. 646
    • Salvador, R.L.1    Saucier, M.2    Simon, D.3    Goyer, R.4
  • 46
    • 0021214351 scopus 로고
    • Nonquaternary cholinesterase reactivators: Heteroaromatic aldoximes as reactivators of ethyl methylphosphonylacetylcholinesterase
    • R.A. Kenely, C.D. Bedford, O.D. Dailey, J.R.A. Howd and A. Miller, Nonquaternary cholinesterase reactivators: Heteroaromatic aldoximes as reactivators of ethyl methylphosphonylacetylcholinesterase, J Med Chem 27 (1984), 1201.
    • (1984) J Med Chem , vol.27 , pp. 1201
    • Kenely, R.A.1    Bedford, C.D.2    Dailey, O.D.3    Howd, J.R.A.4    Miller, A.5
  • 48
    • 0027400808 scopus 로고
    • Jespersen Iodosonaphthoate catalysts for the cleavage of a reactive phosphate
    • R.A. Moss, H. Zhang, S. Chatterjee and K. KroghJespersen, Iodosonaphthoate catalysts for the cleavage of a reactive phosphate, Tetrahedron Lett 34 (1993), 1729.
    • (1993) Tetrahedron Lett , vol.34 , pp. 1729
    • Moss, R.A.1    Zhang, H.2    Chatterjee, S.3    Krogh, K.4
  • 49
    • 0000478330 scopus 로고    scopus 로고
    • Comparative reactivities of phosphotriesters toward iodosocarboxylates in cationic micelles
    • R.A. Moss, A.T. Kotchevar, B.D. Park and P. Scrimin, Comparative reactivities of phosphotriesters toward iodosocarboxylates in cationic micelles, Langmuir 12 (1996), 2200.
    • (1996) Langmuir , vol.12 , pp. 2200
    • Moss, R.A.1    Kotchevar, A.T.2    Park, B.D.3    Scrimin, P.4
  • 51
    • 0035954478 scopus 로고    scopus 로고
    • Catalysis of Phosphate Triester Hydrolysis by micelles of hexadecyltrimethylammonium antipyruvaldehyde 1oximate
    • S. Couderc and J. Toullec, Catalysis of Phosphate Triester Hydrolysis by micelles of hexadecyltrimethylammonium antipyruvaldehyde 1oximate, Langmuir 17 (2001), 3819.
    • (2001) Langmuir , vol.17 , pp. 3819
    • Couderc, S.1    Toullec, J.2
  • 52
    • 23844504377 scopus 로고    scopus 로고
    • A simple approach to azirines containing an aldehyde functionality and their stabilization as palladium II) complexes
    • S. Brahma and J.K. Ray, A simple approach to azirines containing an aldehyde functionality and their stabilization as palladium (II) complexes, Tetrahedron Lett 46 (2005), 6575.
    • (2005) Tetrahedron Lett , vol.46 , pp. 6575
    • Brahma, S.1    Ray, J.K.2
  • 53
    • 11844273847 scopus 로고    scopus 로고
    • Ester cleavage properties of synthetic hydroxybenzotriazoles in cationic monovalent and gemini Surfactant Micelles
    • S. Bhattacharya and P.V. Kumar, Ester cleavage properties of synthetic hydroxybenzotriazoles in cationic monovalent and gemini Surfactant Micelles, Langmuir 21 (2005), 71.
    • (2005) Langmuir , vol.21 , pp. 71
    • Bhattacharya, S.1    Kumar, P.V.2
  • 54
    • 84961986818 scopus 로고    scopus 로고
    • Effect of heteroatom insertion at the side chain of 5alkyl1Htetrazoles on their properties as catalysts for ester hydrolysis at neutral pH
    • S. Bhattacharya and P.K. Vemula, Effect of heteroatom insertion at the side chain of 5alkyl1Htetrazoles on their properties as catalysts for ester hydrolysis at neutral pH, J Org Chem 70 (2005), 9677.
    • (2005) J Org Chem , vol.70 , pp. 9677
    • Bhattacharya, S.1    Vemula, P.K.2
  • 55
    • 37549010735 scopus 로고    scopus 로고
    • Chromogenic and fluorogenic reagents for chemical warfare nerve agents' detection
    • S. Royo, R. MartinezManez, F. Sancenon, A.M. Costero, M. Parra and S. Gil, Chromogenic and fluorogenic reagents for chemical warfare nerve agents' detection, Chem Commun 144 (2007), 4839.
    • (2007) Chem Commun , vol.144 , pp. 4839
    • Royo, S.1    Martinez Manez, R.2    Sancenon, F.3    Costero, A.M.4    Parra, M.5    Gil, S.6
  • 56
    • 77952920115 scopus 로고    scopus 로고
    • Functionalized surfactant mediated reactions of carboxylate, phosphate and sulphonate esters
    • DOI 10.1002/poc.1635
    • S. Tiwari, K.K. Ghosh, J. Marek and K. Kuca, Functionalized surfactant mediated reactions of carboxylate, phosphate and sulphonate esters, J Phys Org Chem 23 (2010), 519. DOI 10.1002/poc.1635.
    • (2010) J Phys Org Chem , vol.23 , pp. 519
    • Tiwari, S.1    Ghosh, K.K.2    Marek, J.3    Kuca, K.4
  • 57
    • 0027281533 scopus 로고
    • Organophosphate poisoning
    • T.C. Marrs, Organophosphate poisoning, Pharmacol Therp 58 (1993), 51.
    • (1993) Pharmacol Therp , vol.58 , pp. 51
    • Marrs, T.C.1
  • 58
    • 18444412899 scopus 로고    scopus 로고
    • Mechanistic studies of La3+and Zn2+catalyzed methanolysis of aryl phosphate and phosphorothioate triesters. Development of artificial phosphotriesterase systems
    • T. Liu, A.A. Neverov, J.S.W. Tsang and R.S. Brown, Mechanistic studies of La3+and Zn2+catalyzed methanolysis of aryl phosphate and phosphorothioate triesters. Development of artificial phosphotriesterase systems, Org Biomol Chem 3 (2005), 1525.
    • (2005) Org Biomol Chem , vol.3 , pp. 1525
    • Liu, T.1    Neverov, A.A.2    Tsang, J.S.W.3    Brown, R.S.4
  • 60
    • 36348939387 scopus 로고    scopus 로고
    • Organophosphate insecticides and acaricides antagonise bifenazate toxicity through esterase inhibition in Tetranychus urticae
    • V.L. Thomas, V.P. Steven, N. Ralf and T. Luc, Organophosphate insecticides and acaricides antagonise bifenazate toxicity through esterase inhibition in Tetranychus urticae, Pest Manag Sci 63 (2007), 1172.
    • (2007) Pest Manag Sci , vol.63 , pp. 1172
    • Thomas, V.L.1    Steven, V.P.2    Ralf, N.3    Luc, T.4
  • 61
    • 33750349896 scopus 로고    scopus 로고
    • Degradation of the pesticide fenitrothion as mediated by cationic surfactants and-nucleophilic reagents
    • X. Han, V.K. Balakrishnan, G.W. VanLoon and E. Buncel, Degradation of the pesticide fenitrothion as mediated by cationic surfactants and-nucleophilic reagents, Langmuir 22 (2006), 9009.
    • (2006) Langmuir , vol.22 , pp. 9009
    • Han, X.1    Balakrishnan, V.K.2    Van Loon, G.W.3    Buncel, E.4
  • 62
    • 0034826043 scopus 로고    scopus 로고
    • Micelles of an oximefunctionalized imidazolium surfactant. Reactivities at phosphoryl and sulfonyl groups
    • Y.S. Simanenko, E.A.Karpichev, T.M. Prokop'eva and B.V. Panchenko,Micelles of an oximefunctionalized imidazolium surfactant. Reactivities at phosphoryl and sulfonyl groups, Langmuir 17 (2001), 581.
    • (2001) Langmuir , vol.17 , pp. 581
    • Simanenko, Y.S.1    Karpichev, E.A.2    Prokop'Eva, T.M.3    Panchenko, B.V.4
  • 64
    • 3543032802 scopus 로고    scopus 로고
    • Functional detergents containing an imidazole ring and typical fragments of-nucleophiles underlying micellar systems for cleavage of esters of prosphorus acids
    • Y.S. Simanenko, E.A. Karpichev, T.M. Prokop'eva, A. Lattes, A.F. Popov, V.A. Savelova and I.A. Belousova, Functional detergents containing an imidazole ring and typical fragments of-nucleophiles underlying micellar systems for cleavage of esters of prosphorus acids, Russ J Org Chem 40 (2004), 206.
    • (2004) Russ J Org Chem , vol.40 , pp. 206
    • Simanenko, Y.S.1    Karpichev, E.A.2    Prokop'Eva, T.M.3    Lattes, A.4    Popov, A.F.5    Savelova, V.A.6    Belousova, I.A.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.