메뉴 건너뛰기




Volumn , Issue , 2014, Pages 9-30

Organic synthesis using an ionic liquid as a reaction medium

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; IONIC LIQUIDS;

EID: 85009232882     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1201/b17508     Document Type: Chapter
Times cited : (2)

References (34)
  • 2
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids. Solvents for synthesis and catalysis
    • Welton, T. 1999. Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chem. Rev. 99: 2071-2083.
    • (1999) Chem. Rev , vol.99 , pp. 2071-2083
    • Welton, T.1
  • 3
    • 0141632776 scopus 로고    scopus 로고
    • Immobilization and reuse of Pd complexes in ionic liquid: Efficient catalytic asymmetric fluorination and Michael reactions with P-ketoesters
    • Hamashima, Y., Takano, H., Hotta, D., and Sodeoka, M. 2003. Immobilization and reuse of Pd complexes in ionic liquid: efficient catalytic asymmetric fluorination and Michael reactions with P-ketoesters. Org. Lett. 5: 3225-3228.
    • (2003) Org. Lett , vol.5 , pp. 3225-3228
    • Hamashima, Y.1    Takano, H.2    Hotta, D.3    Sodeoka, M.4
  • 4
    • 58549085595 scopus 로고    scopus 로고
    • Iron(III) salt-catalyzed Nazarov cyclization/Michael addition of pyrrole derivatives
    • Fujiwara, M., Kawatsura, M., Hayase, S., Nanjo, M., and Itoh, T. 2009. Iron(III) salt-catalyzed Nazarov cyclization/Michael addition of pyrrole derivatives. Adv. Synth. Catal. 351: 123-128.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 123-128
    • Fujiwara, M.1    Kawatsura, M.2    Hayase, S.3    Nanjo, M.4    Itoh, T.5
  • 5
    • 11144299593 scopus 로고    scopus 로고
    • Catalytic asymmetric hydrogenation of aromatic ketones in room temperature ionic liquid
    • Ngo, H., Hu, L. A., and Lin, W. 2005. Catalytic asymmetric hydrogenation of aromatic ketones in room temperature ionic liquid. Tetrahedron Lett. 46: 595-597.
    • (2005) Tetrahedron Lett , vol.46 , pp. 595-597
    • Ngo, H.1    Hu, L.A.2    Lin, W.3
  • 6
    • 67649392916 scopus 로고    scopus 로고
    • Highly enantioselective Ru-catalyzed asymmetric hydrogenation of (P)-keto ester in ionic liquid/methanol mixtures
    • Ochsner, E., Schneiders, K., Junge, K., Beller, M., and Wasserscheid, P. 2009. Highly enantioselective Ru-catalyzed asymmetric hydrogenation of (P)-keto ester in ionic liquid/methanol mixtures. Appl. Catal. A Gen. 364: 8-14.
    • (2009) Appl. Catal. a Gen , vol.364 , pp. 8-14
    • Ochsner, E.1    Schneiders, K.2    Junge, K.3    Beller, M.4    Wasserscheid, P.5
  • 7
    • 78650171639 scopus 로고    scopus 로고
    • Chiral Cu(II) complexes as recyclable catalysts for asymmetric nitroaldol (Henry) reaction in ionic liquids as greener reaction media
    • Khan, H. N-ul., Prasetyanto, E. A., Kim, Y.-K., Ansari, M. B., and Park, S.-E. 2010. Chiral Cu(II) complexes as recyclable catalysts for asymmetric nitroaldol (Henry) reaction in ionic liquids as greener reaction media. Catal. Lett. 140:189-196.
    • (2010) Catal. Lett , vol.140 , pp. 189-196
    • Khan, H.N.1    Prasetyanto, E.A.2    Kim, Y.-K.3    Ansari, M.B.4    Park, S.-E.5
  • 8
    • 0142091320 scopus 로고    scopus 로고
    • Organocatalysis in ionic liquids: Highly efficient L-proline-catalyzed direct asymmetric Mannich reactions involving keton and aldehyde nucleophiles
    • Chowdari, N. S., Ramachary, D. B., and Barbas III, C. F., 2003. Organocatalysis in ionic liquids: highly efficient L-proline-catalyzed direct asymmetric Mannich reactions involving keton and aldehyde nucleophiles. SynLett 1906-1909.
    • (2003) Synlett , pp. 1906-1909
    • Chowdari, N.S.1    Ramachary, D.B.C.F.2
  • 9
    • 3142751057 scopus 로고    scopus 로고
    • Supported ionic liquid asymmetric catalysis. A new method for chiral catalysts recycling. The case of proline-catalyzed aldol reaction
    • Gruttadauria, M., Riela, S., Meo, P. L., D'Anna, F., and Noto, R. 2004. Supported ionic liquid asymmetric catalysis. A new method for chiral catalysts recycling. The case of proline-catalyzed aldol reaction. Tetrahedron Lett. 45: 6113-6116.
    • (2004) Tetrahedron Lett , vol.45 , pp. 6113-6116
    • Gruttadauria, M.1    Riela, S.2    Meo, P.L.3    D'anna, F.4    Noto, R.5
  • 11
    • 33644977649 scopus 로고    scopus 로고
    • Synthetic utilities of ionic liquid-supported NHPI complex
    • Koguchi, S., and Kitazume, T. 2006. Synthetic utilities of ionic liquid-supported NHPI complex. Tetrahedron Lett. 47: 2797-2801.
    • (2006) Tetrahedron Lett , vol.47 , pp. 2797-2801
    • Koguchi, S.1    Kitazume, T.2
  • 12
    • 80052551154 scopus 로고    scopus 로고
    • Recyclable ionic liquid-bridged chiral dimeric salen Mn(III) complexes for oxidative kinetic resolution of racemic secondary alcohols
    • Li, C., Zhao, J., Tan, R., Peng, Z., Luo, R., Peng, M., and Yin, D. 2011. Recyclable ionic liquid-bridged chiral dimeric salen Mn(III) complexes for oxidative kinetic resolution of racemic secondary alcohols. Catal. Commun. 15: 27-31.
    • (2011) Catal. Commun. , vol.15 , pp. 27-31
    • Li, C.1    Zhao, J.2    Tan, R.3    Peng, Z.4    Luo, R.5    Peng, M.6    Yin, D.7
  • 14
    • 84882903692 scopus 로고    scopus 로고
    • Biotransformation in ionic liquid
    • T. Matsuda, 3-20. Elsevier Bioscience, Amsterdam
    • Itoh, T. 2007. Biotransformation in ionic liquid. In Future Directions in Biocatalysis, ed. T. Matsuda, 3-20. Elsevier Bioscience, Amsterdam.
    • (2007) Future Directions in Biocatalysis
    • Itoh, T.1
  • 15
    • 34447136294 scopus 로고    scopus 로고
    • Biocatalysis in ionic liquids
    • van Rantwijk, F., and Sheldon, R. A. 2007. Biocatalysis in ionic liquids. Chem. Rev. 107: 2757-2785.
    • (2007) Chem. Rev , vol.107 , pp. 2757-2785
    • Van Rantwijk, F.1    Sheldon, R.A.2
  • 16
    • 0035532127 scopus 로고    scopus 로고
    • Lipase-catalyzed enantioselective acylation in the ionic liquid solvent system: Reaction of enzyme anchored to the solvent
    • Itoh, T., Akasaki, E., Kudo, K., and Shirakami, S. 2001. Lipase-catalyzed enantioselective acylation in the ionic liquid solvent system: reaction of enzyme anchored to the solvent. Chem. Lett. 262-263.
    • (2001) Chem. Lett , pp. 262-263
    • Itoh, T.1    Akasaki, E.2    Kudo, K.3    Shirakami, S.4
  • 17
    • 1842502863 scopus 로고    scopus 로고
    • Formation and stability of N-heterocyclic carbenes in water: The carbon acid pKa of imidazolium cations in aqueous solution
    • (a) Amyes, T. L., Diver, S. T., Richard, J. P., Rivas, F. M., and Toth, K. 2004. Formation and stability of N-heterocyclic carbenes in water: the carbon acid pKa of imidazolium cations in aqueous solution. J. Am. Chem. Soc. 126, 4366-4374, 2004.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 4366-4374
    • Amyes, T.L.1    Diver, S.T.2    Richard, J.P.3    Rivas, F.M.4    Toth, K.5
  • 18
    • 3242741731 scopus 로고    scopus 로고
    • Basicity of nucleophilic carbenes in aqueous and nonaqueous solvents theoretical predictions
    • (b) Magill, A. M., Cavell, K. J., and Yates, B. F. Basicity of nucleophilic carbenes in aqueous and nonaqueous solvents theoretical predictions. J. Am. Chem. Soc. 126, 8717-8724, 2004.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 8717-8724
    • Magill, A.M.1    Cavell, K.J.2    Yates, B.F.3
  • 19
    • 24744442202 scopus 로고    scopus 로고
    • Magnitude and directionality of interaction in ion pairs of ionic liquids: Relationship with ionic conductivity
    • (c) Tsuzuki, S., Tokuda, H., Hayamizu, K., and Watanabe, M. 2005. Magnitude and directionality of interaction in ion pairs of ionic liquids: relationship with ionic conductivity. J. Phys. Chem. B 109: 16474-16481.
    • (2005) J. Phys. Chem. B , vol.109 , pp. 16474-16481
    • Tsuzuki, S.1    Tokuda, H.2    Hayamizu, K.3    Watanabe, M.4
  • 20
    • 0141888282 scopus 로고    scopus 로고
    • 1-Butyl-2,3-dimethylimidazolium tetrafluoroborate; the most desirable ionic liquid solvent for recycling use of enzyme in lipase-catalyzed transesterification using vinyl acetate as acyl donor
    • Itoh, T., Nishimura, Y., Ouchi, N., and Hayase, S. 2003. 1-Butyl-2,3-dimethylimidazolium tetrafluoroborate; the most desirable ionic liquid solvent for recycling use of enzyme in lipase-catalyzed transesterification using vinyl acetate as acyl donor. J. Mol. Catal. B Enzym. 26: 41-45.
    • (2003) J. Mol. Catal. B Enzym , vol.26 , pp. 41-45
    • Itoh, T.1    Nishimura, Y.2    Ouchi, N.3    Hayase, S.4
  • 21
    • 84864418973 scopus 로고    scopus 로고
    • Ionic liquid engineering for lipase-mediated optical resolution of secondary alcohols: Design of ionic liquids applicable to ionic liquid coated-lipase catalyzed reaction
    • Abe, Y., Yagi, Y., Hayase, S., Kawatsura, M., and Itoh, T. 2012. Ionic liquid engineering for lipase-mediated optical resolution of secondary alcohols: design of ionic liquids applicable to ionic liquid coated-lipase catalyzed reaction. I&EC Res. 51: 9952-9958.
    • (2012) I&Ec Res , vol.51 , pp. 9952-9958
    • Abe, Y.1    Yagi, Y.2    Hayase, S.3    Kawatsura, M.4    Itoh, T.5
  • 23
    • 21844464282 scopus 로고    scopus 로고
    • Friedel-Crafts reactions in room temperature ionic liquids
    • Earle, M. J., Seddon, K. T., Adams, C. J., and Roberts, G. 1998. Friedel-Crafts reactions in room temperature ionic liquids. Chem. Commun. 2097-2098.
    • (1998) Chem. Commun , pp. 2097-2098
    • Earle, M.J.1    Seddon, K.T.2    Adams, C.J.3    Roberts, G.4
  • 24
    • 0037112582 scopus 로고    scopus 로고
    • Ionic liquids containing anionic selenium species: Applications for the oxidative carbonylation of aniline
    • Kim, H. S., Kim, Y. J., Lee, H., and Chin, C. S. 2002. Ionic liquids containing anionic selenium species: applications for the oxidative carbonylation of aniline. Angew. Chem. Int. Ed. 41: 4300-4303.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 4300-4303
    • Kim, H.S.1    Kim, Y.J.2    Lee, H.3    Chin, C.S.4
  • 25
    • 33746216402 scopus 로고    scopus 로고
    • Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins
    • Luo, S. Z., Mi, X. L., Xu, H., Zhang, L., Liu, S., and Cheng, J.-P. 2006. Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins. Angew. Chem. Int. Ed. 45: 3093-3097.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 3093-3097
    • Luo, S.Z.1    Mi, X.L.2    Xu, H.3    Zhang, L.4    Liu, S.5    Cheng, J.-P.6
  • 26
    • 0037019683 scopus 로고    scopus 로고
    • New method of fluorination using potassium fluoride in ionic liquid: Significantly enhanced reactivity of fluoride and improved selectivity
    • Kim, D. W., Song, C. E., and Chi, D. Y. 2002. New method of fluorination using potassium fluoride in ionic liquid: significantly enhanced reactivity of fluoride and improved selectivity. J. Am. Chem. Soc. 124: 10278-10279.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 10278-10279
    • Kim, D.W.1    Song, C.E.2    Chi, D.Y.3
  • 27
    • 33845592524 scopus 로고    scopus 로고
    • A new class of SN2 reactions catalyzed by protic solvents: Facile fluorination for isotopic labeling of diagnostic molecules
    • Kim, D. W., Ahn, D.-S., Oh, Y.-H., Lee, S., Kil, H. S., Oh, S. J., Lee, S. J., Kim, S. J., Ryu, J. S., Moon, D. H., and Chi, D. Y. 2006. A new class of SN2 reactions catalyzed by protic solvents: facile fluorination for isotopic labeling of diagnostic molecules. J. Am. Chem. Soc. 128: 16393-16397.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16393-16397
    • Kim, D.W.1    Ahn, D.-S.2    Oh, Y.-H.3    Lee, S.4    Kil, H.S.5    Oh, S.J.6    Lee, S.J.7    Kim, S.J.8    Ryu, J.S.9    Moon, D.H.10    Chi, D.Y.11
  • 28
    • 0842285877 scopus 로고    scopus 로고
    • Polymer-supported ionic liquids: Imidazolium salts as catalysts for nucleophilic substitution reactions including fluorinations
    • Kim, D. W., and Chi, D. Y. 2004. Polymer-supported ionic liquids: imidazolium salts as catalysts for nucleophilic substitution reactions including fluorinations. Angew. Chem. Int. Ed. 43: 483-485.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 483-485
    • Kim, D.W.1    Chi, D.Y.2
  • 29
    • 0037090118 scopus 로고    scopus 로고
    • Cycloaddition of styrene derivatives with quinone catalyzed by ferric ion; remarkable acceleration in an ionic liquid solvent system
    • Ohara, H., Kiyokane, H., and Itoh, T. 2002. Cycloaddition of styrene derivatives with quinone catalyzed by ferric ion; remarkable acceleration in an ionic liquid solvent system. Tetrahedron Lett. 43: 3041-3044.
    • (2002) Tetrahedron Lett , vol.43 , pp. 3041-3044
    • Ohara, H.1    Kiyokane, H.2    Itoh, T.3
  • 30
    • 13244256940 scopus 로고    scopus 로고
    • Phosphonium ionic liquids as reaction media for strong bases
    • Ramnial, T., Ino, D. D., and Clyburne, J. A. C. 2005. Phosphonium ionic liquids as reaction media for strong bases. Chem. Commun. 325-326.
    • (2005) Chem. Commun , pp. 325-326
    • Ramnial, T.1    Ino, D.D.2    Clyburne, J.A.C.3
  • 31
    • 34848924293 scopus 로고    scopus 로고
    • Design of ionic liquids as reaction media for the Grignard reaction
    • Itoh, T., Kude, K., Hayase, S., and Kawatsura, M. 2007. Design of ionic liquids as reaction media for the Grignard reaction. Tetrahedron Lett. 48: 7774-7777.
    • (2007) Tetrahedron Lett , vol.48 , pp. 7774-7777
    • Itoh, T.1    Kude, K.2    Hayase, S.3    Kawatsura, M.4
  • 32
    • 13844254448 scopus 로고    scopus 로고
    • Iron-catalyzed oxidative homo-coupling of aryl Grignard reagents
    • Nagano, T., and Hayashi, T. 2005. Iron-catalyzed oxidative homo-coupling of aryl Grignard reagents. Org. Lett. 7: 491-493.
    • (2005) Org. Lett , vol.7 , pp. 491-493
    • Nagano, T.1    Hayashi, T.2
  • 33
    • 79959618696 scopus 로고    scopus 로고
    • Iron-catalyzed quick homocoupling reaction of aryl or alkynyl Grignard reagents using a phosphonium ionic liquid solvent system
    • Kude, K., Hayase, S., Kawatsura, M., and Itoh, T. 2011. Iron-catalyzed quick homocoupling reaction of aryl or alkynyl Grignard reagents using a phosphonium ionic liquid solvent system. Heteroatom Chem. 22: 397-404.
    • (2011) Heteroatom Chem , vol.22 , pp. 397-404
    • Kude, K.1    Hayase, S.2    Kawatsura, M.3    Itoh, T.4
  • 34
    • 79959587901 scopus 로고    scopus 로고
    • Catalytic applications of metal nanoparticles in imidazolium ionic liquids
    • Migowski, P., and Dupont, J. 2007. Catalytic applications of metal nanoparticles in imidazolium ionic liquids. Chem Eur J. 13: 13-32.
    • (2007) Chem Eur J , vol.13 , pp. 13-32
    • Migowski, P.1    Dupont, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.