메뉴 건너뛰기




Volumn 13, Issue 13, 2009, Pages 1259-1277

Application of chiral ionic liquids for asymmetric induction in catalysis

Author keywords

[No Author keywords available]

Indexed keywords


EID: 73049094432     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527209789055153     Document Type: Review
Times cited : (55)

References (85)
  • 1
    • 33646453332 scopus 로고    scopus 로고
    • Key technology of the chemical industry - Heterogenic catalysis
    • Schüth, F. Key technology of the chemical industry - Heterogenic catalysis. Chem. Unserer Zeit, 2006, 40, 92-103.
    • (2006) Chem. Unserer Zeit , vol.40 , pp. 92-103
    • Schüth, F.1
  • 6
    • 33746840539 scopus 로고    scopus 로고
    • Asymmetric heterogeneous catalysis
    • Angew. Chem., 2006, 118, 4850-4881. And the references there in
    • Heitbaum, M.; Glorius, F.; Escher, I. Asymmetric heterogeneous catalysis. Angew. Chem. Int. Ed., 2006, 45, 4732-4762, Angew. Chem., 2006, 118, 4850-4881. And the references there in.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 4732-4762
    • Heitbaum, M.1    Glorius, F.2    Escher, I.3
  • 8
    • 38349078806 scopus 로고    scopus 로고
    • Understanding ionic liquids at the molecular level: Facts, problems, and controversies
    • Weingärtner, H. Understanding ionic liquids at the molecular level: Facts, problems, and controversies. Angew. Chem. Int. Ed., 2008, 47, 654-670
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 654-670
    • Weingärtner, H.1
  • 11
    • 33845917900 scopus 로고    scopus 로고
    • Catalytic applications of metal nanoparticles in imidazolium ionic liquids
    • Dupont, J.; Migowski, P. Catalytic applications of metal nanoparticles in imidazolium ionic liquids. Chem.-Eur. J., 2007, 13, 32-39.
    • (2007) Chem. -Eur. J. , vol.13 , pp. 32-39
    • Dupont, J.1    Migowski, P.2
  • 12
    • 33745046627 scopus 로고    scopus 로고
    • Condensed phase behaviour of ionic liquid-benzene mixtures: congruent melting of a [emim][NTf2]center dot C6H6 inclusion crystal
    • Lachwa, J.; Bento, I.; Duarte, M. T.; Lopes, J. N. C.; Rebelo, L. P. N. Condensed phase behaviour of ionic liquid-benzene mixtures: congruent melting of a [emim][NTf2]center dot C6H6 inclusion crystal. Chem. Commun., 2006, 2445-2447.
    • (2006) Chem. Commun. , pp. 2445-2447
    • Lachwa, J.1    Bento, I.2    Duarte, M.T.3    Lopes, J.N.C.4    Rebelo, L.P.N.5
  • 13
    • 33744535443 scopus 로고    scopus 로고
    • Physico-chemical processes in imidazolium ionic liquids
    • Dupont, J.; Suarez, P. A. Z. Physico-chemical processes in imidazolium ionic liquids. Phys. Chem. Chem. Phys., 2006, 8, 2441-2452.
    • (2006) Phys. Chem. Chem. Phys. , vol.8 , pp. 2441-2452
    • Dupont, J.1    Suarez, P.A.Z.2
  • 14
    • 38349047179 scopus 로고    scopus 로고
    • Applications of ionic liquids in the chemical industry
    • For reviews about ILs in general
    • For reviews about ILs in general: (a) Plechkova, N. V.; Seddon, K. R. Applications of ionic liquids in the chemical industry. Chem. Soc. Rev., 2008, 37, 123-150.
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 123-150
    • Plechkova, N.V.1    Seddon, K.R.2
  • 15
    • 35649024841 scopus 로고    scopus 로고
    • Ionic liquids for and by analytical Spectroscopy
    • Tran, C. D. Ionic liquids for and by analytical Spectroscopy. Anal. Lett., 2007, 40, 2447-2464.
    • (2007) Anal. Lett. , vol.40 , pp. 2447-2464
    • Tran, C.D.1
  • 16
    • 34447251884 scopus 로고    scopus 로고
    • Application of ionic liquids of some bioactive molecules in RP-HPLC
    • Polyakova, Y.; Koo, Y. M.; Row, K. H. Application of ionic liquids of some bioactive molecules in RP-HPLC. Rev. Anal. Chem., 2007, 26, 77-98.
    • (2007) Rev. Anal. Chem. , vol.26 , pp. 77-98
    • Polyakova, Y.1    Koo, Y.M.2    Row, K.H.3
  • 17
    • 35649004391 scopus 로고    scopus 로고
    • Asymmetric synthesis in ionic liquids
    • Paczal, A.; Kotschy, A. Asymmetric synthesis in ionic liquids. Monatsh. Chem., 2007, 138, 1115-1123.
    • (2007) Monatsh. Chem. , vol.138 , pp. 1115-1123
    • Paczal, A.1    Kotschy, A.2
  • 18
    • 35148893477 scopus 로고    scopus 로고
    • Ionic liquids in catalytic processes of transformation of olefins and dienes (Review)
    • Nasirov, F. A.; Novruzova, F. M.; Aslanbeili, A. M.; Azizov, A. G. Ionic liquids in catalytic processes of transformation of olefins and dienes (Review). Petroleum Chem., 2007, 47, 309-317.
    • (2007) Petroleum Chem. , vol.47 , pp. 309-317
    • Nasirov, F.A.1    Novruzova, F.M.2    Aslanbeili, A.M.3    Azizov, A.G.4
  • 19
    • 34247203767 scopus 로고    scopus 로고
    • Toward green catalytic synthesis - Transition metalcatalyzed reactions in non-conventional media
    • Liu, S. F.; Xiao, J. L. Toward green catalytic synthesis - Transition metalcatalyzed reactions in non-conventional media. J. Mol. Catal. A: Chem., 2007, 270, 1-43.
    • (2007) J. Mol. Catal. A: Chem. , vol.270 , pp. 1-43
    • Liu, S.F.1    Xiao, J.L.2
  • 20
    • 34447257679 scopus 로고    scopus 로고
    • Advance of room temperature ionic liquid as solvent for extraction and separation
    • Li, Z. J.; Chang, J.; Shan, H. X.; Pan, J. M. Advance of room temperature ionic liquid as solvent for extraction and separation. Rev. Anal. Chem., 2007, 26, 109-153.
    • (2007) Rev. Anal. Chem. , vol.26 , pp. 109-153
    • Li, Z.J.1    Chang, J.2    Shan, H.X.3    Pan, J.M.4
  • 21
    • 34548531154 scopus 로고    scopus 로고
    • A review of ionic liquids towards supercritical fluid applications
    • Keskin, S.; Kayrak-Talay, D.; Akman, U.; Hortacsu, O. A review of ionic liquids towards supercritical fluid applications. J. Supercrit. Fluids, 2007, 43, 150-180.
    • (2007) J. Supercrit. Fluids , vol.43 , pp. 150-180
    • Keskin, S.1    Kayrak-Talay, D.2    Akman, U.3    Hortacsu, O.4
  • 23
    • 34247358600 scopus 로고    scopus 로고
    • Homogeneous catalysis in ionic liquids
    • Giernoth, R. Homogeneous catalysis in ionic liquids. In Situ NMR Methods Catal., 2007, 1-23.
    • (2007) In Situ NMR Methods Catal. , pp. 1-23
    • Giernoth, R.1
  • 24
    • 36248972970 scopus 로고    scopus 로고
    • On the background of enhanced stability and reusability of enzymes in ionic liquids
    • Feher, E.; B. Major, B.; Belafi-Bako, K.; Gubicza, L. On the background of enhanced stability and reusability of enzymes in ionic liquids. Biochem. Soc. Trans., 2007, 35, 1624-1627.
    • (2007) Biochem. Soc. Trans. , vol.35 , pp. 1624-1627
    • Feher, E.B.1    Major, B.2    Belafi-Bako, K.3    Gubicza, L.4
  • 25
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids. Solvents for synthesis and catalysis
    • For reviews also discussing CILs
    • For reviews also discussing CILs: a) Welton, T. Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chem. Rev., 1999, 99, 2071-2083.
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2083
    • Welton, T.1
  • 26
    • 0036809725 scopus 로고    scopus 로고
    • Ionic liquid (molten salt) phase organometallic catalysis
    • Dupont, J.; de Souza, R. F.; Suarez, P. A. Z. Ionic liquid (molten salt) phase organometallic catalysis. Chem. Rev., 2002, 102, 3667-3691.
    • (2002) Chem. Rev. , vol.102 , pp. 3667-3691
    • Dupont, J.1    de Souza, R.F.2    Suarez, P.A.Z.3
  • 28
    • 18144373455 scopus 로고    scopus 로고
    • Chiral ionic liquids: Synthesis and applications
    • Ding, J.; Armstrong, D. W. Chiral ionic liquids: Synthesis and applications. Chirality, 2005, 7, 281-292.
    • (2005) Chirality , vol.7 , pp. 281-292
    • Ding, J.1    Armstrong, D.W.2
  • 29
    • 28844495851 scopus 로고    scopus 로고
    • Chiral ionic liquids, a renewal for the chemistry of chiral solvents? Design, synthesis and applications for chiral recognition and asymmetric synthesis
    • Baudequin, C.; Brégeon, D.; Levillain, J.; Guillen, F.; Plaquevent, J.-C.; Gaumont, A.-C. Chiral ionic liquids, a renewal for the chemistry of chiral solvents? Design, synthesis and applications for chiral recognition and asymmetric synthesis. Tetrahedron Asymmetry, 2005, 16, 3921-3945.
    • (2005) Tetrahedron Asymmetry , vol.16 , pp. 3921-3945
    • Baudequin, C.1    Brégeon, D.2    Levillain, J.3    Guillen, F.4    Plaquevent, J.-C.5    Gaumont, A.-C.6
  • 30
    • 0036998098 scopus 로고    scopus 로고
    • Applications of ionic liquids in organic synthesis
    • Zhao, H.; Malhotra, S. V. Applications of ionic liquids in organic synthesis. Aldrichim. Acta, 2002, 35, 75-83.
    • (2002) Aldrichim. Acta , vol.35 , pp. 75-83
    • Zhao, H.1    Malhotra, S.V.2
  • 31
    • 38349052944 scopus 로고    scopus 로고
    • Advances in chiral ionic liquids derived from natural amino acids
    • Chen, X. W.; Li, X. H.; Hu, A. X.; Wang, F. R. Advances in chiral ionic liquids derived from natural amino acids. Tetrahedron Asymmetry, 2008, 19, 1-14.
    • (2008) Tetrahedron Asymmetry , vol.19 , pp. 1-14
    • Chen, X.W.1    Li, X.H.2    Hu, A.X.3    Wang, F.R.4
  • 32
    • 53749100279 scopus 로고    scopus 로고
    • Applications of chiral ionic liquids
    • Bica, K.; Gaertner, P. Applications of chiral ionic liquids. Eur. J. Org. Chem., 2008, 3235-3250.
    • (2008) Eur. J. Org. Chem. , pp. 3235-3250
    • Bica, K.1    Gaertner, P.2
  • 33
    • 52449087417 scopus 로고    scopus 로고
    • Recent developments on chiral ionic liquids: Design, synthesis, and applications
    • Patil, M.L.; Sasai H. Recent developments on chiral ionic liquids: Design, synthesis, and applications. Chem. Rec., 2008, 8, 98-108.
    • (2008) Chem. Rec. , vol.8 , pp. 98-108
    • Patil, M.L.1    Sasai, H.2
  • 34
    • 38349044351 scopus 로고    scopus 로고
    • Chiral imidazolium ionic liquids: Their synthesis and influence on the outcome of organic reactions. Aldrichim
    • Headley, A.D.; Ni B. Chiral imidazolium ionic liquids: Their synthesis and influence on the outcome of organic reactions. Aldrichim. Acta, 2007, 40, 107-117.
    • (2007) Acta , vol.40 , pp. 107-117
    • Headley, A.D.1    Ni, B.2
  • 35
    • 38349023020 scopus 로고    scopus 로고
    • A novel (S)-proline-modified task-specific chiral ionic liquid -an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water
    • Siyutkin, D. E.; Kucherenko, A. S.; Struchkova, M. I.; Zlotin, S. G. A novel (S)-proline-modified task-specific chiral ionic liquid -an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water. Tetrahedron Lett., 2008, 49, 1212-1216.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1212-1216
    • Siyutkin, D.E.1    Kucherenko, A.S.2    Struchkova, M.I.3    Zlotin, S.G.4
  • 36
    • 33846376783 scopus 로고    scopus 로고
    • Functionalized ionic liquids catalyzed direct aldol reactions
    • Luo, S. Z.; Mi, X. L.; Zhang, L.; Liu, S.; Xu H.; Cheng, J. P. Functionalized ionic liquids catalyzed direct aldol reactions. Tetrahedron, 2007, 63, 1923-1930.
    • (2007) Tetrahedron , vol.63 , pp. 1923-1930
    • Luo, S.Z.1    Mi, X.L.2    Zhang, L.3    Liu, S.4    Xu, H.5    Cheng, J.P.6
  • 37
    • 36648999792 scopus 로고    scopus 로고
    • Functionalized chiral ionic liquid catalyzed enantioselective desymmetrizations of prochiral ketones via asymmetric Michael addition reaction
    • Luo, S. Z.; Zhang, L.; Mi, X. L.; Qiao, Y. P.; Cheng, J. P. Functionalized chiral ionic liquid catalyzed enantioselective desymmetrizations of prochiral ketones via asymmetric Michael addition reaction. J. Org. Chem., 2007, 72, 9350-9352.
    • (2007) J. Org. Chem. , vol.72 , pp. 9350-9352
    • Luo, S.Z.1    Zhang, L.2    Mi, X.L.3    Qiao, Y.P.4    Cheng, J.P.5
  • 38
    • 34250889278 scopus 로고    scopus 로고
    • Effective chirality transfer in ionic liquids through ion-pairing effects
    • Schulz, P. S.; Muller, N.; Bosmann, A.; Wasserscheid, P. Effective chirality transfer in ionic liquids through ion-pairing effects. Angew. Chem. Int. Ed., 2007, 46, 1293-1295.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1293-1295
    • Schulz, P.S.1    Muller, N.2    Bosmann, A.3    Wasserscheid, P.4
  • 39
    • 84982359146 scopus 로고
    • Mechanism of electrochemical pinacolization - 1st asymmetric synthesis in a chiral medium
    • Angew. Chem., 1975, 87, 629-630
    • Seebach, D.; Oei, H. A. Mechanism of electrochemical pinacolization - 1st asymmetric synthesis in a chiral medium. Angew. Chem. Int. Ed., 1975, 14, 634-635; Angew. Chem., 1975, 87, 629-630.
    • (1975) Angew. Chem. Int. Ed. , vol.14 , pp. 634-635
    • Seebach, D.1    Oei, H.A.2
  • 40
    • 4143095848 scopus 로고    scopus 로고
    • First application of chiral ionic liquids in asymmetric Baylis-Hillman reaction
    • Pégot, B.; Vo-Thanh, G.; Gori, D.; Loupy, A. First application of chiral ionic liquids in asymmetric Baylis-Hillman reaction. Tetrahedron Lett. 2004, 6425-6428.
    • (2004) Tetrahedron Lett , pp. 6425-6428
    • Pégot, B.1    Vo-Thanh, G.2    Gori, D.3    Loupy, A.4
  • 42
    • 33744903698 scopus 로고    scopus 로고
    • Simple transformation of crystalline chiral natural anions to liquid medium and their use to induce chirality
    • Bruno, L. C.; Gois, P. M. P.; Lourenço, N. H. T.; Kurteva, V. B.; Afonso, C. A. M. Simple transformation of crystalline chiral natural anions to liquid medium and their use to induce chirality. Chem. Commun., 2006, 2371-2373.
    • (2006) Chem. Commun. , pp. 2371-2373
    • Bruno, L.C.1    Gois, P.M.P.2    Lourenço, N.H.T.3    Kurteva, V.B.4    Afonso, C.A.M.5
  • 43
    • 33646495751 scopus 로고    scopus 로고
    • Application of chiral ionic liquids in the copper catalyzed enantioselective 1,4-addition of diethylzinc to enones
    • Malhotra, S. V.; Wang, Y. Application of chiral ionic liquids in the copper catalyzed enantioselective 1,4-addition of diethylzinc to enones. Tetrahedron Asymmetry, 2006, 17, 1032-1035.
    • (2006) Tetrahedron Asymmetry , vol.17 , pp. 1032-1035
    • Malhotra, S.V.1    Wang, Y.2
  • 44
    • 33746216402 scopus 로고    scopus 로고
    • Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins
    • Angew. Chem., 2006, 118, 3165-3169
    • Luo, S.; Mi, X.; Zhang, L.; Liu, S.; Cheng, J.-P. Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins. Angew. Chem. Int. Ed., 2006, 45, 3093-3097; Angew. Chem., 2006, 118, 3165-3169.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3093-3097
    • Luo, S.1    Mi, X.2    Zhang, L.3    Liu, S.4    Cheng, J.-P.5
  • 45
    • 50049136200 scopus 로고    scopus 로고
    • Chiral ionic liquids for enantioseparation of pharmaceutical products by capillary electrophoresis
    • Tran, C. D.; Mejac, I. Chiral ionic liquids for enantioseparation of pharmaceutical products by capillary electrophoresis. J. Chromatogr. A, 2008, 1204, 204-209.
    • (2008) J. Chromatogr. A , vol.1204 , pp. 204-209
    • Tran, C.D.1    Mejac, I.2
  • 46
    • 57649237758 scopus 로고    scopus 로고
    • The effect of chiral solvent and various kinds of chiral organic salts on the asymmetric hydrogenation of methyl acetoacetate over improved taratraic acid modified raney nickel catalyst
    • Wang, C. F.; Zheng, Y. F.; Cai, S. L.; Ma, J. T.; Li, R. The effect of chiral solvent and various kinds of chiral organic salts on the asymmetric hydrogenation of methyl acetoacetate over improved taratraic acid modified raney nickel catalyst. React. Kinetics Catal. Lett., 2008, 95, 129-134.
    • (2008) React. Kinetics Catal. Lett. , vol.95 , pp. 129-134
    • Wang, C.F.1    Zheng, Y.F.2    Cai, S.L.3    Ma, J.T.4    Li, R.5
  • 47
    • 50049119475 scopus 로고    scopus 로고
    • Preparation and application of a new ion-pairing chiral stationary phase for the liquid chromatographic resolution of N-(3,5-dinitrobenzoyl)-alphaamino acids
    • Hyun, M. H.; Kim, S. N.; Choi, H. J.; Sakthivel, P. Preparation and application of a new ion-pairing chiral stationary phase for the liquid chromatographic resolution of N-(3,5-dinitrobenzoyl)-alphaamino acids. J. Liqu. Chromat. Rel. Technol., 2008, 31, 2363-2374.
    • (2008) J. Liqu. Chromat. Rel. Technol. , vol.31 , pp. 2363-2374
    • Hyun, M.H.1    Kim, S.N.2    Choi, H.J.3    Sakthivel, P.4
  • 48
    • 38549179976 scopus 로고    scopus 로고
    • Synthesis and characterization of novel chiral ionic liquids and investigation of their enantiomeric recognition properties
    • Bwambok, D. K.; Marwani, H. M.; Fernand, V. E.; Fakayode, S. O.; Lowry, M.; Negulescu, I.; Strongin, R. M.; Warner, I. M. Synthesis and characterization of novel chiral ionic liquids and investigation of their enantiomeric recognition properties. Chirality, 2008, 20, 151-158.
    • (2008) Chirality , vol.20 , pp. 151-158
    • Bwambok, D.K.1    Marwani, H.M.2    Fernand, V.E.3    Fakayode, S.O.4    Lowry, M.5    Negulescu, I.6    Strongin, R.M.7    Warner, I.M.8
  • 50
    • 44849094535 scopus 로고    scopus 로고
    • Thiazolinium and imidazolium chiral ionic liquids derived from natural amino acid derivatives
    • Bregeon, D.; Levillain, J.; Guillen, F.; Plaquevent, J. C.; Gaumont, A. C. Thiazolinium and imidazolium chiral ionic liquids derived from natural amino acid derivatives. Amino Acids, 2008, 35, 175-184.
    • (2008) Amino Acids , vol.35 , pp. 175-184
    • Bregeon, D.1    Levillain, J.2    Guillen, F.3    Plaquevent, J.C.4    Gaumont, A.C.5
  • 51
    • 39049155856 scopus 로고    scopus 로고
    • Synthesis of new chiral ionic liquids based on (-)-menthol and (-)-borneol
    • Matos, R. A. F.; Andrade, C. K. Z. Synthesis of new chiral ionic liquids based on (-)-menthol and (-)-borneol Tetrahedron Lett., 2008, 49, 1652-1655.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1652-1655
    • Matos, R.A.F.1    Andrade, C.K.Z.2
  • 52
    • 47749088989 scopus 로고    scopus 로고
    • Synthesis and properties of novel chiral ionic liquids from L-proline
    • Gao, H. S.; Hu, Z. G.; Wang, J. J.; Qiu, Z. F.; Fan, F. Q. Synthesis and properties of novel chiral ionic liquids from L-proline. Austr. J. Chem., 2008, 61, 521-525.
    • (2008) Austr. J. Chem. , vol.61 , pp. 521-525
    • Gao, H.S.1    Hu, Z.G.2    Wang, J.J.3    Qiu, Z.F.4    Fan, F.Q.5
  • 53
    • 0041880138 scopus 로고    scopus 로고
    • Ionic liquids are not always green: hydrolysis of 1-butyl-3-methylimidazolium hexafluorophosphate
    • Swatloski, R. P.; Holbrey, J. D.; Rogers, R. D. Ionic liquids are not always green: hydrolysis of 1-butyl-3-methylimidazolium hexafluorophosphate. Green Chem., 2003, 5, 361-363.
    • (2003) Green Chem. , vol.5 , pp. 361-363
    • Swatloski, R.P.1    Holbrey, J.D.2    Rogers, R.D.3
  • 54
    • 15744383666 scopus 로고    scopus 로고
    • Chiral phosphine lewis bases catalyzed asymmetric aza-Baylis-Hiliman reaction of N-sulfonated imines with activated olefins J
    • Shi, M.; Chen, L.-H.; Li, C.-Q. Chiral phosphine lewis bases catalyzed asymmetric aza-Baylis-Hiliman reaction of N-sulfonated imines with activated olefins J. Am. Chem. Soc., 2005, 127, 3790-3800.
    • (2005) Am. Chem. Soc. , vol.127 , pp. 3790-3800
    • Shi, M.1    Chen, L.-H.2    Li, C.-Q.3
  • 55
    • 15744396095 scopus 로고    scopus 로고
    • Bifunctional organocatalysts for enantioselective aza-Morita-Baylis-Hillman reaction
    • Matsui, K.; Takizawa, S.; Sanai, H. Bifunctional organocatalysts for enantioselective aza-Morita-Baylis-Hillman reaction. J. Am. Chem. Soc., 2005, 127, 3680-3681.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3680-3681
    • Matsui, K.1    Takizawa, S.2    Sanai, H.3
  • 56
    • 49549109600 scopus 로고    scopus 로고
    • Design and synthesis of bistereogenic chiral ionic liquids and their use as solvents for asymmetric Baylis-Hillman reactions
    • Garre, S.; Parker, E.; Ni, B. K.; Headley, A. D. Design and synthesis of bistereogenic chiral ionic liquids and their use as solvents for asymmetric Baylis-Hillman reactions. Org. Biomol. Chem., 2008, 6, 3041-3043.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 3041-3043
    • Garre, S.1    Parker, E.2    Ni, B.K.3    Headley, A.D.4
  • 57
    • 34547357512 scopus 로고    scopus 로고
    • Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes
    • Ni, B.; Zhang, Q.; Headley, A. D. Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes. Green Chem., 2007, 9, 737-739.
    • (2007) Green Chem. , vol.9 , pp. 737-739
    • Ni, B.1    Zhang, Q.2    Headley, A.D.3
  • 58
    • 48949114906 scopus 로고    scopus 로고
    • A mild and efficient procedure for asymmetric Michael additions of cyclohexanone to chalcones catalyzed by an amino acid ionic liquid
    • Qian, Y. B.; Xiao, S. Y.; Liu, L.; Wang, Y. M. A mild and efficient procedure for asymmetric Michael additions of cyclohexanone to chalcones catalyzed by an amino acid ionic liquid. Tetrahedron-Asymmetry, 2008, 19, 1515-1518.
    • (2008) Tetrahedron-Asymmetry , vol.19 , pp. 1515-1518
    • Qian, Y.B.1    Xiao, S.Y.2    Liu, L.3    Wang, Y.M.4
  • 59
    • 38349049059 scopus 로고    scopus 로고
    • Pyrrolidine-based chiral pyridinium ionic liquids (ILs) as recyclable and highly efficient organocatalysts for the asymmetric Michael addition reactions
    • Ni, B. K.; Zhang, Q. Y.; Headley, A. D. Pyrrolidine-based chiral pyridinium ionic liquids (ILs) as recyclable and highly efficient organocatalysts for the asymmetric Michael addition reactions. Tetrahedron Lett., 2008, 49, 1249-1252.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1249-1252
    • Ni, B.K.1    Zhang, Q.Y.2    Headley, A.D.3
  • 60
    • 64349100404 scopus 로고    scopus 로고
    • Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins
    • Ni, B. K.; Zhang, Q. Y.; Dhungana, K.; Headley, A. D. Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins. Org. Lett., 2009, 11, 1037-1040.
    • (2009) Org. Lett. , vol.11 , pp. 1037-1040
    • Ni, B.K.1    Zhang, Q.Y.2    Dhungana, K.3    Headley, A.D.4
  • 61
    • 42749087995 scopus 로고    scopus 로고
    • Asymmetric Michael addition reactions of aldehydes with nitrostyrenes catalyzed by functionalized chiral ionic liquids
    • Zhang, Q. Y.; Ni, B. K.; Headley, A. D. Asymmetric Michael addition reactions of aldehydes with nitrostyrenes catalyzed by functionalized chiral ionic liquids. Tetrahedron, 2008, 64, 5091-5097.
    • (2008) Tetrahedron , vol.64 , pp. 5091-5097
    • Zhang, Q.Y.1    Ni, B.K.2    Headley, A.D.3
  • 62
    • 48949121232 scopus 로고    scopus 로고
    • Polymer-immobilized pyrrolidine-based chiral ionic liquids as recyclable organocatalysts for asymmetric Michael additions to nitrostyrenes under solventfree reaction conditions
    • Li, P. H.; Wang, L.; Wang, M.; Zhang, Y. C. Polymer-immobilized pyrrolidine-based chiral ionic liquids as recyclable organocatalysts for asymmetric Michael additions to nitrostyrenes under solventfree reaction conditions. Eur. J. Org. Chem., 2008, 1157-1160.
    • (2008) Eur. J. Org. Chem. , pp. 1157-1160
    • Li, P.H.1    Wang, L.2    Wang, M.3    Zhang, Y.C.4
  • 63
    • 45649083198 scopus 로고    scopus 로고
    • Silica gel supported pyrrolidine-based chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes
    • Li, P. H.; Wang, L.; Zhang, Y. C.; Wang, G. W. Silica gel supported pyrrolidine-based chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes. Tetrahedron, 2008, 64, 7633-7638.
    • (2008) Tetrahedron , vol.64 , pp. 7633-7638
    • Li, P.H.1    Wang, L.2    Zhang, Y.C.3    Wang, G.W.4
  • 64
    • 33746728262 scopus 로고    scopus 로고
    • An efficient and practical synthesis of chiral imidazolium ionic liquids and their application in an enantioselective Michael reaction
    • Ou, W.-H.; Huang, Z. Z. An efficient and practical synthesis of chiral imidazolium ionic liquids and their application in an enantioselective Michael reaction. Green Chem., 2006, 8, 731-734.
    • (2006) Green Chem. , vol.8 , pp. 731-734
    • Ou, W.-H.1    Huang, Z.Z.2
  • 65
    • 20344398647 scopus 로고    scopus 로고
    • Synthesis of new chiral ionic liquids from natural acids and their applications in enantioselective Michael addition
    • Wang, Z. M.; Wang, Q.; Zhang, Y.; Bao, W. L. Synthesis of new chiral ionic liquids from natural acids and their applications in enantioselective Michael addition. Tetrahedron Lett., 2005, 46, 4657-4660.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 4657-4660
    • Wang, Z.M.1    Wang, Q.2    Zhang, Y.3    Bao, W.L.4
  • 66
    • 57549115024 scopus 로고    scopus 로고
    • A highly efficient and recyclable ionic liquid anchored pyrrolidine catalyst for enantioselective Michael additions
    • Miao, T.; Wang, L.; Li P. H.; Yan J. C. A highly efficient and recyclable ionic liquid anchored pyrrolidine catalyst for enantioselective Michael additions. Synthesis, 2008, 23, 3828-3834.
    • (2008) Synthesis , vol.23 , pp. 3828-3834
    • Miao, T.1    Wang L2    Li, P.H.3    Yan, J.C.4
  • 67
    • 33748281160 scopus 로고    scopus 로고
    • Ionic-liquid-supported organocatalyst: Efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction
    • Miao, W.; Chan, T. H. Ionic-liquid-supported organocatalyst: Efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction. Adv. Synth. Catal., 2006, 348, 1711-1718.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 1711-1718
    • Miao, W.1    Chan, T.H.2
  • 68
    • 58149352252 scopus 로고    scopus 로고
    • Hydroxy-alphaamino acids modified by ionic liquid moieties: recoverable organocatalysts for asymmetric aldol reactions in the presence of water
    • Siyutkin, D. E.; Kucherenko, A. S.; Zlotin, S. G. Hydroxy-alphaamino acids modified by ionic liquid moieties: recoverable organocatalysts for asymmetric aldol reactions in the presence of water. Tetrahedron, 2009, 65, 1366-1372.
    • (2009) Tetrahedron , vol.65 , pp. 1366-1372
    • Siyutkin, D.E.1    Kucherenko, A.S.2    Zlotin, S.G.3
  • 69
    • 38349023020 scopus 로고    scopus 로고
    • A novel (S)-proline-modified task-specific chiral ionic liquid -an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water
    • Siyutkin, D. E.; Kucherenko, A. S.; Struchkova, M. I.; Zlotin, S. G., A novel (S)-proline-modified task-specific chiral ionic liquid -an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water. Tetrahedron Lett., 2008, 49, 1212-1216.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1212-1216
    • Siyutkin, D.E.1    Kucherenko, A.S.2    Struchkova, M.I.3    Zlotin, S.G.4
  • 70
    • 49349104098 scopus 로고    scopus 로고
    • Pronounced ionic liquid effect in the synthesis of biologically active isatin-3-oxime derivatives under acid catalysis
    • Pinto, A. C.; Lapis, A. A. M.; da Silva, B. V.; Bastos, R. S.; Dupont, J.; Neto, B. A. D. Pronounced ionic liquid effect in the synthesis of biologically active isatin-3-oxime derivatives under acid catalysis. Tetrahedron Lett., 2008, 49, 5639-5641.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 5639-5641
    • Pinto, A.C.1    Lapis, A.A.M.2    da Silva, B.V.3    Bastos, R.S.4    Dupont, J.5    Neto, B.A.D.6
  • 71
    • 38549121798 scopus 로고    scopus 로고
    • Combinatorial synthesis of functionalized chiral and doubly chiral ionic liquids and their applications as asymmetric covalent/non-covalent bifunctional organocatalysts
    • Zhang, L.; Luo, S. Z.; Mi, X. L.; Liu, S.; Qiao, Y. P.; Xu, H.; Cheng, J. P. Combinatorial synthesis of functionalized chiral and doubly chiral ionic liquids and their applications as asymmetric covalent/non-covalent bifunctional organocatalysts. Org. Biomol. Chem., 2008, 6, 567-576.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 567-576
    • Zhang, L.1    Luo, S.Z.2    Mi, X.L.3    Liu, S.4    Qiao, Y.P.5    Xu, H.6    Cheng, J.P.7
  • 72
    • 54149117629 scopus 로고    scopus 로고
    • Direct asymmetric aldol reaction catalyzed by an imidazolium-tagged trans-4-Hydroxy-L-proline under aqueous biphasic conditions
    • Lombardo, M.; Pasi, F.; Easwar S. Trombini C. Direct asymmetric aldol reaction catalyzed by an imidazolium-tagged trans-4-Hydroxy-L-proline under aqueous biphasic conditions. Synlett, 2008, 16, 2471-2474.
    • (2008) Synlett , vol.16 , pp. 2471-2474
    • Lombardo, M.1    Pasi F2    Easwar, S.3    Trombini, C.4
  • 73
    • 38849159924 scopus 로고    scopus 로고
    • Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions
    • Zhou, W.; Xu, L. W.; Qiu, H. Y.; Lai G. Q.; Xia C. G.; Jiang J. X. Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions. Helv. Chim. Acta, 2008, 91, 53-59.
    • (2008) Helv. Chim. Acta , vol.91 , pp. 53-59
    • Zhou, W.1    Xu, L.W.2    Qiu H.Y3    Lai, G.Q.4    Xia, C.G.5    Jiang, J.X.6
  • 76
    • 68349130923 scopus 로고    scopus 로고
    • Enantioselective hydrogenation with racemic and enantiopure binap in the presence of a chiral ionic liquid
    • Chen, D.; Schmitkamp, M.; Franciò, G.; Klankermayer, J.; Leitner., W. Enantioselective hydrogenation with racemic and enantiopure binap in the presence of a chiral ionic liquid. Angew. Chem., 2008, 120, 7449 -7451.
    • (2008) Angew. Chem. , vol.120 , pp. 7449-7451
    • Chen, D.1    Schmitkamp, M.2    Franciò, G.3    Klankermayer, J.4    Leitner, W.5
  • 77
    • 35848939801 scopus 로고    scopus 로고
    • Enantio selective phase transfer alkylation using orthopalladated complex in chiral ionic liquid
    • Mukherjee, D. K.; Ghosh, N. Enantio selective phase transfer alkylation using orthopalladated complex in chiral ionic liquid. Catal. Commun., 2008, 9, 40-44.
    • (2008) Catal. Commun. , vol.9 , pp. 40-44
    • Mukherjee, D.K.1    Ghosh, N.2
  • 78
    • 60949086716 scopus 로고    scopus 로고
    • Chirality transfer in imidazolium camphorsulfonate ionic liquids through ion pairing effects
    • Schneiders, K.; Boesmann, A.; Schulz, P. S.; Wasserscheid, P. Chirality transfer in imidazolium camphorsulfonate ionic liquids through ion pairing effects. Adv. Synth. Catal., 2009, 351, 432-440.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 432-440
    • Schneiders, K.1    Boesmann, A.2    Schulz, P.S.3    Wasserscheid, P.4
  • 79
    • 33749658984 scopus 로고    scopus 로고
    • Asymmetric aza-Diels-Alder reaction of Danishefsky's diene with imines in a chiral reaction medium
    • article-no 18. doi: 10.1186/1860-5297-2-18
    • Pégot, B.; Van Buu, O. N.; Gori, D.; Vo-Thanh, G. Asymmetric aza-Diels-Alder reaction of Danishefsky's diene with imines in a chiral reaction medium. Beilstein J. Org. Chem., 2006, 2, article-no 18. doi: 10.1186/1860-5297-2-18.
    • (2006) Beilstein J. Org. Chem.
    • Pégot, B.1    Van Buu, O.N.2    Gori, D.3    Vo-Thanh, G.4
  • 80
    • 59749098452 scopus 로고    scopus 로고
    • Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels-Alder reaction
    • Van Buu, O. N.; Aupoix, A.; Vo-Thanh, G. Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels-Alder reaction. Tetrahedron, 2009, 65, 2260-2265.
    • (2009) Tetrahedron , vol.65 , pp. 2260-2265
    • Van Buu, O.N.1    Aupoix, A.2    Vo-Thanh, G.3
  • 81
    • 35649010410 scopus 로고    scopus 로고
    • Synthesis of novel chiral ammonium-based ionic liquids derived from hosorbide and their applications in an asymmetric aza Diels-Alder reaction
    • Van Buu, O. N.; Vo-Thanh, G. Synthesis of novel chiral ammonium-based ionic liquids derived from hosorbide and their applications in an asymmetric aza Diels-Alder reaction. Lett. Org. Chem., 2007, 4, 158-167.
    • (2007) Lett. Org. Chem. , vol.4 , pp. 158-167
    • Van Buu, O.N.1    Vo-Thanh, G.2
  • 82
    • 34249054958 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of camphor-derived chiral imidazolium ionic liquids and their application in diastereoselective Diels-Alder reaction
    • Bica, K.; Gmeiner, G.; Reichel, C.; Lendl, B.; Gaertner, P. Microwave-assisted synthesis of camphor-derived chiral imidazolium ionic liquids and their application in diastereoselective Diels-Alder reaction. Synthesis, 2007, 1333-1338.
    • (2007) Synthesis , pp. 1333-1338
    • Bica, K.1    Gmeiner, G.2    Reichel, C.3    Lendl, B.4    Gaertner, P.5
  • 83
    • 0037124758 scopus 로고    scopus 로고
    • Asymmetric hydrogenations (Nobel lecture)
    • Nobel lectures 2001 about asymmetric catalysis Angew. Chem. 2002 114 2001 2096- 2107
    • Nobel lectures 2001 about asymmetric catalysis: a) Knowles, W. S. Asymmetric hydrogenations (Nobel lecture). Angew. Chem. Int. Ed., 2002, 1998-2007; Angew. Chem., 2002, 114, 2096-2107.
    • (2002) Angew Chem. Int. Ed. , pp. 1998-2007
    • Knowles, W.S.1
  • 84
    • 0037124885 scopus 로고    scopus 로고
    • Asymmetric catalysis: Science and opportunities (Nobel lecture)
    • Angew. Chem., 2002, 114, 2108- 2123
    • Noyori, R. Asymmetric catalysis: Science and opportunities (Nobel lecture). Angew. Chem. Int. Ed., 2002, 2008-2022, Angew. Chem., 2002, 114, 2108- 2123.
    • (2002) Angew. Chem. Int. Ed. , pp. 2008-2022
    • Noyori, R.1
  • 85
    • 0037124794 scopus 로고    scopus 로고
    • Searching for new reactivity (Nobel lecture)
    • Angew. Chem., 2002, 114, 2126-2135
    • Sharpless, K. B. Searching for new reactivity (Nobel lecture). Angew. Chem. Int. Ed., 2002, 2024-2032; Angew. Chem., 2002, 114, 2126-2135.
    • (2002) Angew. Chem. Int. Ed. , pp. 2024-2032
    • Sharpless, K.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.