메뉴 건너뛰기




Volumn 45, Issue 5, 2006, Pages 1594-1603

Improved conversion and selectivity of a Diels-Alder cycloaddition by use of emulsions of carbon dioxide and water

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIVITY; DIELS-ALDER CYCLOADDITION; LIQUID CARBON DIOXIDE; SUPERCRITICAL CARBON DIOXIDE;

EID: 33645013318     PISSN: 08885885     EISSN: None     Source Type: Journal    
DOI: 10.1021/ie0507225     Document Type: Article
Times cited : (10)

References (79)
  • 1
    • 33847085398 scopus 로고
    • Hydrophobic acceleration of DielsAlder reactions
    • Rideout, D. C.; Breslow, R. Hydrophobic Acceleration of DielsAlder Reactions. J. Am. Chem. Soc. 1980, 102, 7816.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 7816
    • Rideout, D.C.1    Breslow, R.2
  • 2
    • 0001300546 scopus 로고
    • Selective Diels-Alder reactions in aqueous solutions and suspensions
    • Breslow, R.; Maitra, U.; Rideout, D. Selective Diels-Alder Reactions in Aqueous Solutions and Suspensions. Tetrahedron Lett. 1983, 24, 1901.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 1901
    • Breslow, R.1    Maitra, U.2    Rideout, D.3
  • 3
    • 0000659379 scopus 로고
    • On the origin of product selectivity in aqueous Diels-Alder reactions
    • Breslow, R.; Maitra, U. Tetrahedron Lett. On the Origin of Product Selectivity in Aqueous Diels-Alder Reactions. 1984, 25, 1239.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 1239
    • Breslow, R.1    Maitra, U.2
  • 4
    • 33845280668 scopus 로고
    • Diels-Alder reactions in nonaqueous polar solvents. Kinetic effects of chaotropic and antichaotropic agents and of β-cyclodextrin
    • Breslow, R.; Guo, T. Diels-Alder Reactions in Nonaqueous Polar Solvents. Kinetic Effects of Chaotropic and Antichaotropic Agents and of β-Cyclodextrin. J. Am. Chem. Soc. 1988, 110, 5613.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5613
    • Breslow, R.1    Guo, T.2
  • 5
    • 12044255058 scopus 로고
    • Hydrophobic effects on simple organic reactions in water
    • Breslow, R. Hydrophobic Effects on Simple Organic Reactions in Water. Acc. Chem. Res. 1991, 24, 159.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 159
    • Breslow, R.1
  • 6
    • 84918189424 scopus 로고
    • Chaotropic salt effects in a hydrophobically accelerated Diels-Alder reaction
    • Breslow, R.; Rizzo, C. J. Chaotropic Salt Effects in a Hydrophobically Accelerated Diels-Alder Reaction. J. Am. Chem. Soc. 1991, 113, 4340.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4340
    • Breslow, R.1    Rizzo, C.J.2
  • 7
    • 0000586983 scopus 로고
    • Quantitative antihydrophobic effects as probes for transition state structures. 2. Diels-Alder reactions
    • Breslow, R.; Zhu, Z. Quantitative Antihydrophobic Effects as Probes for Transition State Structures. 2. Diels-Alder Reactions. J. Am. Chem. Soc. 1995, 117, 9923.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 9923
    • Breslow, R.1    Zhu, Z.2
  • 8
    • 3242699566 scopus 로고    scopus 로고
    • Determining the geometries of transition state by use of antihydrophobic additives to water
    • Breslow, R. Determining the Geometries of Transition State by Use of Antihydrophobic Additives to Water. Acc. Chem. Res. 2004, 37, 471.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 471
    • Breslow, R.1
  • 9
    • 0000619653 scopus 로고
    • "Micellar" catalysis in the aqueous intermolecular Diels-Alder reaction: Rate acceleration and enhanced selectivity
    • Grieco, P. A.; Garner, P.; He, Z. "Micellar" Catalysis in the Aqueous Intermolecular Diels-Alder Reaction: Rate Acceleration and Enhanced Selectivity. Tetrahedron Lett. 1983, 24, 1897.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 1897
    • Grieco, P.A.1    Garner, P.2    He, Z.3
  • 10
    • 33845551929 scopus 로고
    • Aqueous intermolecular Diels-Alder chemistry: Reactions of diene carboxlates with dienophiles in water at ambient temperature
    • Grieco, P. A.; Yoshida, K.; Garner, P. Aqueous Intermolecular Diels-Alder Chemistry: Reactions of Diene Carboxlates with Dienophiles in Water at Ambient Temperature. J. Org. Chem. 1983, 48, 3137.
    • (1983) J. Org. Chem. , vol.48 , pp. 3137
    • Grieco, P.A.1    Yoshida, K.2    Garner, P.3
  • 11
    • 0001734272 scopus 로고
    • Sodium 6-methoy-(E,E)-3,5-hexadienoate: A useful diene in the intermolecular Diels-Alder reaction
    • Grieco, P. A.; Yoshida, K.; He, Z. Tetrahedron Lett. Sodium 6-Methoy-(E,E)-3,5-Hexadienoate: A Useful Diene in the Intermolecular Diels-Alder Reaction. 1984, 25, 5715.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5715
    • Grieco, P.A.1    Yoshida, K.2    He, Z.3
  • 12
    • 33845378798 scopus 로고
    • Aza Diels-Alder reactions in aqueous solution: Cyclocondensation of dienes with simple iminium salts generated under mannich conditions
    • Larsen, S. D.; Grieco, P. A. Aza Diels-Alder Reactions in Aqueous Solution: Cyclocondensation of Dienes with Simple Iminium Salts Generated under Mannich Conditions. J. Am. Chem. Soc. 1985, 107, 1768.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 1768
    • Larsen, S.D.1    Grieco, P.A.2
  • 13
    • 0000274359 scopus 로고
    • Aqueous intermolecular Diels-Alder chemistry. Reaction of (E)-2,4-pentadienyl ammonium chloride and related ammonium salts with dienophiles in water
    • Grieco, P. A.: Galatsis, P.; Spohn, R. F. Aqueous Intermolecular Diels-Alder Chemistry. Reaction of (E)-2,4-pentadienyl ammonium chloride and related ammonium salts with dienophiles in water. Tetrahedron 1986, 42, 2847.
    • (1986) Tetrahedron , vol.42 , pp. 2847
    • Grieco, P.A.1    Galatsis, P.2    Spohn, R.F.3
  • 14
    • 0004252595 scopus 로고    scopus 로고
    • Grieco, P. A., Ed.; Blackie Academic and Professional: New York
    • Organic Synthesis in Water, Grieco, P. A., Ed.; Blackie Academic and Professional: New York, 1998.
    • (1998) Organic Synthesis in Water
  • 15
    • 0000945578 scopus 로고
    • Diels-Alder reaction in aqueous solutions. Enforced hydrophobic interactions between diene and dienophile
    • Blokzilj, W.; Blandamer, M. J.; Engberts, J. B. F. N. Diels-Alder Reaction in Aqueous Solutions. Enforced Hydrophobic Interactions between Diene and Dienophile. J. Am. Chem. Soc. 1991, 113, 4241.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4241
    • Blokzilj, W.1    Blandamer, M.J.2    Engberts, J.B.F.N.3
  • 16
    • 0000888091 scopus 로고
    • Initial-state and transition-state effects on Diels-Alder reactions in water and mixed aqueous solvents
    • Blokzilj, W.; Engberts, J. B. F. N. Initial-State and Transition-State Effects on Diels-Alder Reactions in Water and Mixed Aqueous Solvents. J. Am. Chem. Soc. 1992, 114, 5440.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5440
    • Blokzilj, W.1    Engberts, J.B.F.N.2
  • 17
    • 33646934177 scopus 로고
    • Diels-Alder reactions in water. Effects of hydrophobicity and hydrogen bonding
    • Otto, S.; Blokzilj, W.; Engberts, J. B. F. N. Diels-Alder Reactions in Water. Effects of Hydrophobicity and Hydrogen Bonding. J. Org. Chem. 1994, 59, 5372.
    • (1994) J. Org. Chem. , vol.59 , pp. 5372
    • Otto, S.1    Blokzilj, W.2    Engberts, J.B.F.N.3
  • 18
    • 0001864639 scopus 로고
    • Enforced hydrophobic interactions and hydrogen-bonding in the acceleration of Diels-Alder reactions in water
    • Cremer, C. J., Truhlar, D. G., Eds.; ACS Symposium Series No. 568; American Chemical Society: Washington. DC. Chapter 21
    • Blokzilj, W.; Engberts, J. B. F. N. Enforced Hydrophobic Interactions and Hydrogen-Bonding in the Acceleration of Diels-Alder Reactions in Water. In Structure and Reactivity in Aqueous Solution; Cremer, C. J., Truhlar, D. G., Eds.; ACS Symposium Series No. 568; American Chemical Society: Washington. DC. 1994; Chapter 21, pp 303-317.
    • (1994) Structure and Reactivity in Aqueous Solution , pp. 303-317
    • Blokzilj, W.1    Engberts, J.B.F.N.2
  • 19
    • 0000641247 scopus 로고    scopus 로고
    • Solvent effects on a Diels-Alder reaction involving a cationic diene: Consequences of the absence of hydrogen-bond interactions for accelerations in aqueous media
    • van der Wel, G. K.; Wijnen, J. W.; Engberts, J. B. F. N. Solvent Effects on a Diels-Alder Reaction Involving a Cationic Diene: Consequences of the Absence of Hydrogen-Bond Interactions for Accelerations in Aqueous Media. J. Org. Chem. 1996, 61, 9001.
    • (1996) J. Org. Chem. , vol.61 , pp. 9001
    • Van Der Wel, G.K.1    Wijnen, J.W.2    Engberts, J.B.F.N.3
  • 20
    • 0000726870 scopus 로고    scopus 로고
    • Retro-Diels-Alder reaction in aqueous solution: Toward a better understanding of organic reactivity in water
    • Wijnen. J. W.; Engberts, J. B. F. N. Retro-Diels-Alder Reaction in Aqueous Solution: Toward a Better Understanding of Organic Reactivity in Water. J. Org. Chem. 1997, 62, 2039.
    • (1997) J. Org. Chem. , vol.62 , pp. 2039
    • Wijnen, J.W.1    Engberts, J.B.F.N.2
  • 21
    • 0031763196 scopus 로고    scopus 로고
    • Effects of the hydrophobicity of the reactants on Diels-Alder Reactions in water
    • Meijer, A.; Otto, S.; Engberts, J. B. F. N. Effects of the Hydrophobicity of the Reactants on Diels-Alder Reactions in Water. J. Org. Chem. 1998, 63, 8989.
    • (1998) J. Org. Chem. , vol.63 , pp. 8989
    • Meijer, A.1    Otto, S.2    Engberts, J.B.F.N.3
  • 23
    • 0035929133 scopus 로고    scopus 로고
    • Understanding organic reactions in water: From hydrophobic encounters to surfactant aggregates
    • Engberts, J. B. F. N.; Blandamer, M. J. Understanding Organic Reactions in Water: From Hydrophobic Encounters to Surfactant Aggregates. Chem. Commun. 2001, 1701.
    • (2001) Chem. Commun. , pp. 1701
    • Engberts, J.B.F.N.1    Blandamer, M.J.2
  • 24
    • 0001230190 scopus 로고
    • Glyco-organic substrates in organic synthesis. Preparation of a water soluble butadienyl-ether and its use in aqueous cycloaddition
    • Lubineau, A.; Queneau, Y. Glyco-Organic Substrates in Organic Synthesis. Preparation of a Water Soluble Butadienyl-Ether and Its Use in Aqueous Cycloaddition. Tetrahedron Lett. 1985, 26, 2653.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 2653
    • Lubineau, A.1    Queneau, Y.2
  • 26
    • 0000764456 scopus 로고
    • Aqueous cyloadditions using glyco-organic substrates - Thermodynamics of the reaction
    • Lubineau, A.; Bienaymé, H.; Queneau, Y.; Scherrmann, M. C. Aqueous Cyloadditions Using Glyco-Organic Substrates - Thermodynamics of the Reaction. New J. Chem. 1994, 18, 279.
    • (1994) New J. Chem. , vol.18 , pp. 279
    • Lubineau, A.1    Bienaymé, H.2    Queneau, Y.3    Scherrmann, M.C.4
  • 27
    • 0002287474 scopus 로고    scopus 로고
    • Water as a solvent in organic synthesis
    • Lubineau, A.; Auge, J. Water as a Solvent in Organic Synthesis. Top. Curr. Chem. 1999, 206, 1.
    • (1999) Top. Curr. Chem. , vol.206 , pp. 1
    • Lubineau, A.1    Auge, J.2
  • 28
    • 84942724676 scopus 로고
    • Diels-Alder reactions in hydrophobie cavities: A quantitative correlation with solvophobicity and rate enhancements by macrocycles
    • Schneider, H.-J.; Sangwan, N. K. Diels-Alder Reactions in Hydrophobie Cavities: A Quantitative Correlation with Solvophobicity and Rate Enhancements by Macrocycles. J. Chem. Soc., Chem Commun. 1986, 1787.
    • (1986) J. Chem. Soc., Chem Commun. , pp. 1787
    • Schneider, H.-J.1    Sangwan, N.K.2
  • 29
    • 0023617690 scopus 로고
    • Changes of stereoselectivity in Diels-Alder reactions by hydophobic solvents effects and by β-cyclodextrin
    • Schneider, H.-J.; Sangwan, N. K. Changes of Stereoselectivity in Diels-Alder Reactions by Hydophobic Solvents Effects and by β-Cyclodextrin. Angew. Chem., Int. Ed. Engl. 1987, 26, 896.
    • (1987) Angew. Chem., Int. Ed. Engl. , vol.26 , pp. 896
    • Schneider, H.-J.1    Sangwan, N.K.2
  • 30
    • 37049067073 scopus 로고
    • The kinetic effects of water and cylodextrins on Diels-Alder reactions. host-guest chemistry. Part 18
    • Sangwan, N. K.; Schneider, H.-J. The Kinetic Effects of Water and Cylodextrins on Diels-Alder Reactions. Host-Guest Chemistry. Part 18. J Chem. Soc., Perkins Trans. 2 1989, 1223.
    • (1989) J Chem. Soc., Perkins Trans. 2 , pp. 1223
    • Sangwan, N.K.1    Schneider, H.-J.2
  • 31
    • 0001653096 scopus 로고
    • Solvent effects on a Diels-Alder reaction from computer simulation
    • Blake, J. F.; Jorgensen, W. L. Solvent Effects on a Diels-Alder Reaction from Computer Simulation. J. Am. Chem. Soc. 1991, 113, 7430.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7430
    • Blake, J.F.1    Jorgensen, W.L.2
  • 32
    • 0000193645 scopus 로고
    • Ab initio study of dielsalder reactions of cyclopentadiene with ethylene. Isoprene, cyclopentadiene, acrylonitrile, and methyl vinyl ketone
    • Jorgensen, W. L.; Lim, D.; Blake, J. F. Ab Initio Study of DielsAlder Reactions of Cyclopentadiene with Ethylene. Isoprene, Cyclopentadiene, Acrylonitrile, and Methyl Vinyl Ketone. J. Am. Chem. Soc. 1993, 115, 2936.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2936
    • Jorgensen, W.L.1    Lim, D.2    Blake, J.F.3
  • 33
    • 0000886146 scopus 로고
    • Enhanced hydrogen bonding of water to Diels-Alder transition states. Ab initio evidence
    • Blake, J. F.; Lim, D.; Jorgensen, W. L. Enhanced Hydrogen Bonding of Water to Diels-Alder Transition States. Ab Initio Evidence. J. Org. Chem. 1994, 59, 803.
    • (1994) J. Org. Chem. , vol.59 , pp. 803
    • Blake, J.F.1    Lim, D.2    Jorgensen, W.L.3
  • 34
    • 0037158732 scopus 로고    scopus 로고
    • QM/MM simulations for Diels-Alder reactions in water: Contribution of enhanced hydrogen bonding at the transition state to the solvent effect
    • Chandrasekhar, J.; Shariffskul, S.; Jorgensen, W. L. QM/MM Simulations for Diels-Alder Reactions in Water: Contribution of Enhanced Hydrogen Bonding at the Transition State to the Solvent Effect. J. Phys. Chem. B 2002, 106, 8078.
    • (2002) J. Phys. Chem. B , vol.106 , pp. 8078
    • Chandrasekhar, J.1    Shariffskul, S.2    Jorgensen, W.L.3
  • 35
    • 0001571717 scopus 로고    scopus 로고
    • Hydrophobic and hydrogen-bonding effects on the rate of Diels-Alder reactions in aqueous solution
    • Furlani, T. R.; Gao, J. Hydrophobic and Hydrogen-Bonding Effects on the Rate of Diels-Alder Reactions in Aqueous Solution. J. Org. Chem. 1996, 61, 5492.
    • (1996) J. Org. Chem. , vol.61 , pp. 5492
    • Furlani, T.R.1    Gao, J.2
  • 36
    • 0001279445 scopus 로고    scopus 로고
    • Reactive flux calculations of methyl vinyl ketone reacting with cylcopentadiene in water
    • Pak, Y.; Voth, G. A. Reactive Flux Calculations of Methyl Vinyl Ketone Reacting with Cylcopentadiene in Water. J. Phys. Chem. A 1999, 103, 925.
    • (1999) J. Phys. Chem. A , vol.103 , pp. 925
    • Pak, Y.1    Voth, G.A.2
  • 37
    • 0034715486 scopus 로고    scopus 로고
    • Density functional theory study of aqueous-phase rate acceleration and endo/exo selectivity of the butadiene and acrolein Diels-Alder reaction
    • Kong, S.; Evanseck, J. D. Density Functional Theory Study of Aqueous-Phase Rate Acceleration and Endo/Exo Selectivity of the Butadiene and Acrolein Diels-Alder Reaction. J. Am. Chem. Soc. 2000, 122, 10418.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10418
    • Kong, S.1    Evanseck, J.D.2
  • 38
    • 4644277320 scopus 로고    scopus 로고
    • The influence of water on the rates of 1,3-dipolar cycloaddition reactions: Trigger points for exponential rate increases in water - organic solvent mixtures. Water-super versus water-normal dipolarophiles
    • Butler, R. N.; Cunningham, W. J.; Coyne, A. G.; Burke, L. A. The Influence of Water on the Rates of 1,3-Dipolar Cycloaddition Reactions: Trigger Points for Exponential Rate Increases in Water - Organic Solvent Mixtures. Water-Super versus Water-Normal Dipolarophiles. J. Am. Chem. Soc. 2004, 126, 11923.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 11923
    • Butler, R.N.1    Cunningham, W.J.2    Coyne, A.G.3    Burke, L.A.4
  • 39
    • 0000252506 scopus 로고    scopus 로고
    • Catalysis of Diels-Alder reactions in water and hydrogen-bonding environments
    • Rappaport, Z., Ed.; John Wiley and Sons, Ltd.: New York, Chapter 13
    • Witkopp, A.; Schreiner, P. R. Catalysis of Diels-Alder Reactions in Water and Hydrogen-Bonding Environments. In The Chemistry of Dienes and Polyenes; Rappaport, Z., Ed.; John Wiley and Sons, Ltd.: New York, 2000; Vol. 2, Chapter 13, pp 1029-1088.
    • (2000) The Chemistry of Dienes and Polyenes , vol.2 , pp. 1029-1088
    • Witkopp, A.1    Schreiner, P.R.2
  • 40
    • 0000677232 scopus 로고
    • Organic reaction in aqueous media - With a focus on carbon-carbon bond formation
    • Li, C.-J. Organic Reaction in Aqueous Media - With a Focus on Carbon-Carbon Bond Formation. Chem. Rev. 1993, 93, 2023.
    • (1993) Chem. Rev. , vol.93 , pp. 2023
    • Li, C.-J.1
  • 42
    • 0001427514 scopus 로고
    • The correlation of solvent effects on the stereoselectivities of Diels-Alder reactions by means of linear free energy relationships. A new empirical measure of solvent polarity
    • Berson, J. A.; Hamlet, Z.; Mueller, W. A. The Correlation of Solvent Effects on the Stereoselectivities of Diels-Alder Reactions by Means of Linear Free Energy Relationships. A New Empirical Measure of Solvent Polarity. J. Am. Chem. Soc. 1962, 84, 297.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 297
    • Berson, J.A.1    Hamlet, Z.2    Mueller, W.A.3
  • 43
    • 0141852842 scopus 로고    scopus 로고
    • A study of solvent effects on the stereoselectivity of Diels-Alder reactions through molecular surface electrostatic potentials
    • Gholami, M. R.; Talebi, B. A.: Khalili, M. A Study of Solvent Effects on the Stereoselectivity of Diels-Alder Reactions through Molecular Surface Electrostatic Potentials. Tetrahedron Lett. 2003, 44, 7681.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 7681
    • Gholami, M.R.1    Talebi, B.A.2    Khalili, M.3
  • 44
    • 0029813957 scopus 로고    scopus 로고
    • Lewis acid catalysis of a Diels-Alder reaction in water
    • Otto, S.; Bertoncin, F.; Engberts, J. B. F. N. Lewis Acid Catalysis of a Diels-Alder Reaction in Water. J. Am. Chem. Soc. 1996, 118, 7702.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7702
    • Otto, S.1    Bertoncin, F.2    Engberts, J.B.F.N.3
  • 45
    • 0001648506 scopus 로고    scopus 로고
    • A chiral lewis-acid-catalyzed Diels-Alder reaction. Water enhanced enantioselectivity
    • Otto, S.; Boccaletti, G.; Engberts, J. B. F. N. A Chiral Lewis-Acid-Catalyzed Diels-Alder Reaction. Water Enhanced Enantioselectivity. J. Am. Chem. Soc. 1998, 120, 4238.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4238
    • Otto, S.1    Boccaletti, G.2    Engberts, J.B.F.N.3
  • 46
    • 0032560981 scopus 로고    scopus 로고
    • Million-fold acceleration of a Diels-Alder reaction due to combined lewis acid and micellar catalysis in water
    • Otto, S.; Engberts, J. B. F. N.; Kwak, J. C. T. Million-Fold Acceleration of a Diels-Alder Reaction due to Combined Lewis Acid and Micellar Catalysis in Water. J. Am. Chem. Soc. 1998, 120, 9517.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 9517
    • Otto, S.1    Engberts, J.B.F.N.2    Kwak, J.C.T.3
  • 47
    • 0033612740 scopus 로고    scopus 로고
    • A systematic sutdy of the ligand effects on a lewis-acid-catalyzed Diels-Alder reaction in water. Water-enhanced enantioselectivity
    • Otto, S.; Engberts, J. B. F. N. A Systematic Sutdy of the Ligand Effects on a Lewis-Acid-Catalyzed Diels-Alder Reaction in Water. Water-Enhanced Enantioselectivity. J. Am. Chem. Soc. 1999, 121, 6798.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6798
    • Otto, S.1    Engberts, J.B.F.N.2
  • 48
    • 0000662767 scopus 로고    scopus 로고
    • Efficient catalysis of a Diels-Alder reaction by métallo-vesicles in aqueous solution
    • Rispens, T.; Engberts, J. B. F. N. Efficient Catalysis of a Diels-Alder Reaction by Métallo-Vesicles in Aqueous Solution. Org. Lett. 2001, 3, 941.
    • (2001) Org. Lett. , vol.3 , pp. 941
    • Rispens, T.1    Engberts, J.B.F.N.2
  • 49
    • 0032499046 scopus 로고    scopus 로고
    • Studies on the use of surfactants in aqueous Diels-Alder reactions
    • Diego-Castro, M. J.; Hailes, H. C. Studies on the Use of Surfactants in Aqueous Diels-Alder Reactions. Tetrahedron Lett. 1998, 39, 2211.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2211
    • Diego-Castro, M.J.1    Hailes, H.C.2
  • 50
    • 0033543484 scopus 로고    scopus 로고
    • Effects of lewis-acid-surfactant-combined catalysts on aldol and Diels-Alder reactions in water
    • Manabe, K.; Mori, Y.; Kobayashi, S. Effects of Lewis-Acid-Surfactant- Combined Catalysts on Aldol and Diels-Alder Reactions in Water. Tetrahedron 1999, 55, 11203.
    • (1999) Tetrahedron , vol.55 , pp. 11203
    • Manabe, K.1    Mori, Y.2    Kobayashi, S.3
  • 51
    • 0034596298 scopus 로고    scopus 로고
    • Organic synthesis inside particles in water: Lewis acid-surfactant- combined catalysts for organic reactions in water using colloidal dispersions as reaction media
    • Manabe, K.; Mori, Y.; Wakabayashi, T.; Nagayama, S.; Kobayashi, S. Organic Synthesis Inside Particles in Water: Lewis Acid-Surfactant-Combined Catalysts for Organic Reactions in Water Using Colloidal Dispersions as Reaction Media. J. Am. Chem. Soc. 2000, 122, 7202.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7202
    • Manabe, K.1    Mori, Y.2    Wakabayashi, T.3    Nagayama, S.4    Kobayashi, S.5
  • 52
    • 0036105107 scopus 로고    scopus 로고
    • Development of novel lewis acid catalysts for selective organic reaction in aqueous media
    • Kobayashi, S.; Manabe, K. Development of Novel Lewis Acid Catalysts for Selective Organic Reaction in Aqueous Media. Acc. Chem. Res. 2002, 35, 209.
    • (2002) Acc. Chem. Res. , vol.35 , pp. 209
    • Kobayashi, S.1    Manabe, K.2
  • 54
    • 0041672516 scopus 로고    scopus 로고
    • Ultrasonic emulsification of liquid, near-critical carbon dioxide-water biphasic mixtures for acceleration of a hydrolysis reaction
    • Timko, M. T.; Diffendal, J. M.; Tester, J. W.: Smith, K. A.; Peters, W. A.; Danheiser, R. L.; Steinfeld, J. I. Ultrasonic Emulsification of Liquid, Near-Critical Carbon Dioxide-Water Biphasic Mixtures for Acceleration of a Hydrolysis Reaction. J. Phys. Chem. A 2003, 107, 5503.
    • (2003) J. Phys. Chem. A , vol.107 , pp. 5503
    • Timko, M.T.1    Diffendal, J.M.2    Tester, J.W.3    Smith, K.A.4    Peters, W.A.5    Danheiser, R.L.6    Steinfeld, J.I.7
  • 55
    • 33645010553 scopus 로고    scopus 로고
    • Emulsions of dense carbon dioxide and water formed using power ultrasound: Mass transport and reactor design
    • accepted for publication in November
    • Timko, M. T.; Danheiser, R. L.; Steinfeld, J. I.; Tester, J. W.; Smith, K. A. Emulsions of Dense Carbon Dioxide and Water Formed Using Power Ultrasound: Mass Transport and Reactor Design. AIChE J., accepted for publication in November, 2005.
    • (2005) AIChE J.
    • Timko, M.T.1    Danheiser, R.L.2    Steinfeld, J.I.3    Tester, J.W.4    Smith, K.A.5
  • 57
    • 0034843113 scopus 로고    scopus 로고
    • Surfactants and self-assembly in carbon dioxide
    • and references therein
    • DeSimone, J. M.; Keiper, J. S. Surfactants and Self-Assembly in Carbon Dioxide. Curr. Opin. Solid State Mater. Sci. 2001, 5, 333 and references therein.
    • (2001) Curr. Opin. Solid State Mater. Sci. , vol.5 , pp. 333
    • DeSimone, J.M.1    Keiper, J.S.2
  • 62
    • 0001272467 scopus 로고    scopus 로고
    • Mechanistic and spatial study of ultrasonically induced luminol chemiluminescence
    • McMurray, H. N.; Wilson, B. P. Mechanistic and Spatial Study of Ultrasonically Induced Luminol Chemiluminescence. J. Phys. Chem. A 1999, 103, 3955.
    • (1999) J. Phys. Chem. A , vol.103 , pp. 3955
    • McMurray, H.N.1    Wilson, B.P.2
  • 63
    • 0030817473 scopus 로고    scopus 로고
    • Ultrasonically enhanced corrosion of 304L stainless steel. 2. The effect of frequency, acoustic power and horn to specimen distance
    • Whillock, G. O. H.; Harvey, B. F. Ultrasonically Enhanced Corrosion of 304L Stainless Steel. 2. The Effect of Frequency, Acoustic Power and Horn to Specimen Distance. Ultrason. Sonochem. 1997, 4, 33.
    • (1997) Ultrason. Sonochem. , vol.4 , pp. 33
    • Whillock, G.O.H.1    Harvey, B.F.2
  • 64
    • 0032021574 scopus 로고    scopus 로고
    • Modeling of three-dimensional linear pressure fields in sonochemical reactors with homogeneous and inhoraogeneous density distributions of cavitation bubbles
    • Dähnke, S.; Keil, F. J. Modeling of Three-Dimensional Linear Pressure Fields in Sonochemical Reactors with Homogeneous and Inhoraogeneous Density Distributions of Cavitation Bubbles. Ind. Eng. Chem. Res. 1998, 37, 848.
    • (1998) Ind. Eng. Chem. Res. , vol.37 , pp. 848
    • Dähnke, S.1    Keil, F.J.2
  • 65
    • 0033104479 scopus 로고    scopus 로고
    • Modeling of three-dimensional pressure fields in sonochemical reactors with an inhomogeneous density distribution of cavitation bubbles. Comparison of theoretical and experimental results
    • Dähnke, S.; Swaray, K. M.; Keil, F. J. Modeling of Three-Dimensional Pressure Fields in Sonochemical Reactors with an Inhomogeneous Density Distribution of Cavitation Bubbles. Comparison of Theoretical and Experimental Results. Ultrason. Sonochem. 1999, 6, 31.
    • (1999) Ultrason. Sonochem. , vol.6 , pp. 31
    • Dähnke, S.1    Swaray, K.M.2    Keil, F.J.3
  • 68
    • 0037902592 scopus 로고
    • Sonochemistry
    • Suslick, K. S. Sonochemistry. Science 1990, 247, 1439.
    • (1990) Science , vol.247 , pp. 1439
    • Suslick, K.S.1
  • 70
  • 72
    • 0000954719 scopus 로고
    • Multiphase high-pressure equilibria of carbon dioxide-water-acetone
    • Wendland, M.; Hasse, H.; Maurer, G. Multiphase High-Pressure Equilibria of Carbon Dioxide-Water-Acetone. J. Supercrit. Fluids 1994, 7, 245.
    • (1994) J. Supercrit. Fluids , vol.7 , pp. 245
    • Wendland, M.1    Hasse, H.2    Maurer, G.3
  • 73
    • 0033592174 scopus 로고    scopus 로고
    • Use of scandium tri(trifluoromethanesulfonate) as a lewis acid catalyst in supercritical carbon dioxide: Efficient Diels-Alder reactions and pressure dependent enhancement of endo:exo stereoselectivity
    • Oakes, R. S.; Heppenstall, T. J.; Shezad, N.; Clifford, A. A.; Rayner, C. M. Use of Scandium Tri(trifluoromethanesulfonate) as a Lewis Acid Catalyst in Supercritical Carbon Dioxide: Efficient Diels-Alder Reactions and Pressure Dependent Enhancement of Endo:exo Stereoselectivity. Chem. Commun. 1999, 1459.
    • (1999) Chem. Commun. , pp. 1459
    • Oakes, R.S.1    Heppenstall, T.J.2    Shezad, N.3    Clifford, A.A.4    Rayner, C.M.5
  • 74
    • 3342945299 scopus 로고    scopus 로고
    • Partition coefficients of organic solutes between supercritical carbon dioxide and water: Experimental measurements and empirical correlations
    • Timko, M. T.; Nicholson, B. F.; Steinfeld, J. I.; Smith, K. A.; Tester, J. W. Partition Coefficients of Organic Solutes between Supercritical Carbon Dioxide and Water: Experimental Measurements and Empirical Correlations. J. Chem. Eng. Data 2004, 49, 768.
    • (2004) J. Chem. Eng. Data , vol.49 , pp. 768
    • Timko, M.T.1    Nicholson, B.F.2    Steinfeld, J.I.3    Smith, K.A.4    Tester, J.W.5
  • 78
    • 0002841874 scopus 로고    scopus 로고
    • Emulsion formation
    • Binks, B. P., Ed.; The Royal Society of Chemistry: Cambridge, U.K.
    • Walstra, P.; Smulders, P. E. A. Emulsion Formation. In Modern Aspects of Emulsion Science; Binks, B. P., Ed.; The Royal Society of Chemistry: Cambridge, U.K., 1998.
    • (1998) Modern Aspects of Emulsion Science
    • Walstra, P.1    Smulders, P.E.A.2
  • 79
    • 0031249640 scopus 로고    scopus 로고
    • Sonochemical reactions at 640 kHz using an efficient reactor. Oxidation of potassium iodide
    • Seymour, J. D.; Wallace, H. C.; Gupta, R. B. Sonochemical Reactions at 640 kHz Using an Efficient Reactor. Oxidation of Potassium Iodide. Ultrason. Sonochem. 1997, 4, 289.
    • (1997) Ultrason. Sonochem. , vol.4 , pp. 289
    • Seymour, J.D.1    Wallace, H.C.2    Gupta, R.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.