메뉴 건너뛰기




Volumn , Issue , 2011, Pages 209-256

Synthesis of Chiral Catalysts Supported on Organic Polymers

Author keywords

Chiral catalyst synthesis supported on organic polymers; Chiral catalysts on organic polymers, bottom up strategies macromolecular synthesis and catalyst immobilization; Organometallic chiral catalysts, binap catalysts expedient manner, limited by aromatic nature

Indexed keywords


EID: 84864760986     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118087992.ch4     Document Type: Chapter
Times cited : (9)

References (97)
  • 2
    • 0036810665 scopus 로고    scopus 로고
    • Recoverable catalysts for asymmetric organic synthesis
    • Fan, Q.-H., Li, Y.-M., Chan, A. S. C. (2002). Recoverable catalysts for asymmetric organic synthesis. Chem. Rev., 102, 3385-3466.
    • (2002) Chem. Rev., , vol.102 , pp. 3385-3466
    • Fan, Q.-H.1    Li, Y.-M.2    Chan, A.S.C.3
  • 6
    • 0033186074 scopus 로고    scopus 로고
    • Matrix assisted synthetic transformations: a mosaic of diverse contributions
    • Hudson, D. (1999). Matrix assisted synthetic transformations: a mosaic of diverse contributions. I. The pattern emerges. J. Comb. Chem., 1, 333-360.
    • (1999) I. The pattern emerges. J. Comb. Chem. , vol.1 , pp. 333-360
    • Hudson, D.1
  • 7
    • 65349139123 scopus 로고    scopus 로고
    • Organic polymer supports for synthesis and for reagent and catalyst immobilization
    • Lu, J., Toy, P. H. (2009). Organic polymer supports for synthesis and for reagent and catalyst immobilization. Chem. Rev., 109, 815-838. For more references.
    • (2009) Chem. Rev , vol.109 , pp. 815-838
    • Lu, J.1    Toy, P.H.2
  • 8
    • 20744456789 scopus 로고
    • Solid phase peptide synthesis I: the synthesis of a tetrapeptide
    • Merrifield; see: Merrifi eld, R. B. (1963). Solid phase peptide synthesis I: the synthesis of a tetrapeptide. J. Am. Chem. Soc., 85, 2149-2154.
    • (1963) J. Am. Chem. Soc., , vol.85 , pp. 2149-2154
    • Merrifield, R.B.1
  • 11
    • 37049139019 scopus 로고
    • The asymmetric synthesis of hydratropic acid and amino-acids by homogeneous catalytic hydrogenation
    • Dang, T.-P., Kagan, H. (1971). The asymmetric synthesis of hydratropic acid and amino-acids by homogeneous catalytic hydrogenation. J. Chem. Soc. Chem. Commun., 481.
    • (1971) J Chem. Soc. Chem. Commun. , pp. 481
    • Dang, T.-P.1    Kagan, H.2
  • 12
    • 33847800667 scopus 로고
    • Asymmetric hydrogenation with a complex of rhodium and a chiral bisphosphine
    • Knowles, W. S., Sabacky, M. J., Vineyard, B. D., Weinkauff, D. J. (1975). Asymmetric hydrogenation with a complex of rhodium and a chiral bisphosphine. J. Am. Chem. Soc., 97, 2567-2568.
    • (1975) J. Am. Chem. Soc., , vol.97 , pp. 2567-2568
    • Knowles, W.S.1    Sabacky, M.J.2    Vineyard, B.D.3    Weinkauff, D.J.4
  • 13
    • 1542694981 scopus 로고
    • Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of alpha.-(acylamino)acrylic acids
    • Miyashita, A., Yasuda, A., Takaya, H., Toriumi, K., Ito, T., Souchi, T., Noyori, R. (1980). Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of alpha.-(acylamino)acrylic acids. J. Am. Chem. Soc., 102, 7932-7934.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 7932-7934
    • Miyashita, A.1    Yasuda, A.2    Takaya, H.3    Toriumi, K.4    Ito, T.5    Souchi, T.6    Noyori, R.7
  • 14
    • 0032368051 scopus 로고    scopus 로고
    • The enantioselective hydrogenation of N-acyl dehydroamino acids
    • Nagel, U., Albrecht, J. (1998). The enantioselective hydrogenation of N-acyl dehydroamino acids. Top. Catal., 5, 3-23.
    • (1998) Top. Catal., , vol.5 , pp. 3-23
    • Nagel, U.1    Albrecht, J.2
  • 16
    • 0001352945 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of ketones with polymer-bound BINAP/diamine ruthenium catalysts
    • Ohkuma, T., Takeno, H., Honda, Y., Noyori, R. (2001). Asymmetric hydrogenation of ketones with polymer-bound BINAP/diamine ruthenium catalysts. Adv. Synth. Catal., 343, 369-375.
    • (2001) Adv. Synth. Catal., , vol.343 , pp. 369-375
    • Ohkuma, T.1    Takeno, H.2    Honda, Y.3    Noyori, R.4
  • 17
    • 0033527705 scopus 로고    scopus 로고
    • Palladium diaqua and hydroxo complexes with polymer-supported BINAP ligands and their use for catalytic enantioselective reactions
    • Fujii, A., Sodeoka, M. (1999). Palladium diaqua and hydroxo complexes with polymer-supported BINAP ligands and their use for catalytic enantioselective reactions. Tetrahedron Lett., 40, 8011-8014.
    • (1999) Tetrahedron Lett., , vol.40 , pp. 8011-8014
    • Fujii, A.1    Sodeoka, M.2
  • 18
    • 0037420809 scopus 로고    scopus 로고
    • Synthesis of enantiopure 1,2-diamine attached to cross-linked polystyrene and its application to an insoluble catalyst for asymmetric hydrogenation
    • Itsuno, S., Tsuji, A., Takahashi, M. (2003). Synthesis of enantiopure 1,2-diamine attached to cross-linked polystyrene and its application to an insoluble catalyst for asymmetric hydrogenation. Tetrahedron Lett., 44, 3825-3828.
    • (2003) Tetrahedron Lett., , vol.44 , pp. 3825-3828
    • Itsuno, S.1    Tsuji, A.2    Takahashi, M.3
  • 19
    • 0032547030 scopus 로고    scopus 로고
    • Synthesis and evaluation of a chiral heterogeneous transfer hydrogenation catalyst
    • Bayston, D. J., Travers, C. B., Polywka, M. E. C. (1998). Synthesis and evaluation of a chiral heterogeneous transfer hydrogenation catalyst. Tetrahedron Asymmetry, 9, 2015-2018.
    • (1998) Tetrahedron Asymmetry, , vol.9 , pp. 2015-2018
    • Bayston, D.J.1    Travers, C.B.2    Polywka, M.E.C.3
  • 20
    • 23044484402 scopus 로고    scopus 로고
    • Preparation of polymer-supported Ru-TsDPEN catalysts and use for enantioselective synthesis of (S)-fl uoxetine
    • Li, Y., Li, Z., Li, F., Wang, Q., Tao, F. (2005). Preparation of polymer-supported Ru-TsDPEN catalysts and use for enantioselective synthesis of (S)-fl uoxetine. Org. Biomol. Chem., 3, 2513-2518.
    • (2005) Org. Biomol. Chem., , vol.3 , pp. 2513-2518
    • Li, Y.1    Li, Z.2    Li, F.3    Wang, Q.4    Tao, F.5
  • 21
    • 0002760696 scopus 로고    scopus 로고
    • A novel chiral water-soluble phosphine ligand based on a water-soluble acrylic acid salt
    • Malmström, T., Andersson, C. (1996). A novel chiral water-soluble phosphine ligand based on a water-soluble acrylic acid salt. Chem. Commun., 1135-1136.
    • (1996) Chem. Commun , pp. 1135-1136
    • Malmström, T.1    Andersson, C.2
  • 22
    • 8744230576 scopus 로고    scopus 로고
    • Asymmetric processes catalyzed by chiral (salen)metal complexes
    • For a review of asymmetric processes catalyzed by chiral salen metal complexes, see: Larrow, J. F., Jacobsen, E. N. (2004). Asymmetric processes catalyzed by chiral (salen)metal complexes. Top. Organomet. Chem., 6, 123-152.
    • (2004) Top. Organomet. Chem., , vol.6 , pp. 123-152
    • Larrow, J.F.1    Jacobsen, E.N.2
  • 23
    • 0032495094 scopus 로고    scopus 로고
    • Remarkable matrix effect in polymer-supported Jacobsen' s alkene epoxidation catalysts
    • Canali, L., Cowan, E., Deleuze, H., Gibson, C. L., Sherrington, D. C. (1998). Remarkable matrix effect in polymer-supported Jacobsen' s alkene epoxidation catalysts. Chem. Commun., 2561-2562.
    • (1998) Chem. Commun., , pp. 2561-2562
    • Canali, L.1    Cowan, E.2    Deleuze, H.3    Gibson, C.L.4    Sherrington, D.C.5
  • 24
    • 0032480681 scopus 로고    scopus 로고
    • Synthesis and characterization of a polymer - supported salen ligand for enantioselective epoxidation
    • Angelino, M. D., Laibinis, P. E. (1998). Synthesis and characterization of a polymer - supported salen ligand for enantioselective epoxidation. Macromolecules, 31, 7581-7587.
    • (1998) Macromolecules, , vol.31 , pp. 7581-7587
    • Angelino, M.D.1    Laibinis, P.E.2
  • 25
    • 0033526360 scopus 로고    scopus 로고
    • Polymer-supported chiral Co(salen) complexes: synthetic applications and mechanistic investigations in the hydrolytic kinetic resolution of terminal epoxides
    • Annis, D. A., Jacobsen, E. N. (1999). Polymer-supported chiral Co(salen) complexes: synthetic applications and mechanistic investigations in the hydrolytic kinetic resolution of terminal epoxides. J. Am. Chem. Soc., 121, 4147-4154.
    • (1999) J. Am. Chem. Soc., , vol.121 , pp. 4147-4154
    • Annis, D.A.1    Jacobsen, E.N.2
  • 26
    • 0034718088 scopus 로고    scopus 로고
    • Polymer-supported (salen)Mn catalysts for asymmetric epoxidation: a comparison between soluble and insoluble matrices
    • Reger, T. S., Janda, K. D. (2000). Polymer-supported (salen)Mn catalysts for asymmetric epoxidation: a comparison between soluble and insoluble matrices. J. Am. Chem. Soc., 122, 6929-6934.
    • (2000) J. Am. Chem. Soc., , vol.122 , pp. 6929-6934
    • Reger, T.S.1    Janda, K.D.2
  • 27
    • 0002958115 scopus 로고    scopus 로고
    • Heterogeneous asymmetric epoxidation of alkenes catalysed by a polymer-bound (pyrrolidine salen)manganese(III) complex
    • Song, C. E., Roh, E. J., Yu, B. M., Chi, D. Y., Kim, S. C., Lee, K.-J. (2000). Heterogeneous asymmetric epoxidation of alkenes catalysed by a polymer-bound (pyrrolidine salen)manganese(III) complex. Chem. Commun., 615-616.
    • (2000) Chem. Commun., , pp. 615-616
    • Song, C.E.1    Roh, E.J.2    Yu, B.M.3    Chi, D.Y.4    Kim, S.C.5    Lee, K.-J.6
  • 28
    • 0037149979 scopus 로고    scopus 로고
    • Asymmetric epoxidation using a singly-bound supported Katsuki-type (salen)Mn complex
    • Smith, K., Liu, C.-H. (2002). Asymmetric epoxidation using a singly-bound supported Katsuki-type (salen)Mn complex. Chem. Commun., 886-887.
    • (2002) Chem. Commun., , pp. 886-887
    • Smith, K.1    Liu, C.-H.2
  • 30
    • 0013465429 scopus 로고    scopus 로고
    • Preparation and catalytic properties of immobilized chiral dirhodium(II) carboxamidates
    • Doyle, M. P., Timmons, D. J., Tumonis, J. S., Gau, H.-M., Blossey, E. C. (2002). Preparation and catalytic properties of immobilized chiral dirhodium(II) carboxamidates . Organometallics, 21, 1747-1749.
    • (2002) Organometallics, , vol.21 , pp. 1747-1749
    • Doyle, M.P.1    Timmons, D.J.2    Tumonis, J.S.3    Gau, H.-M.4    Blossey, E.C.5
  • 31
    • 0037071932 scopus 로고    scopus 로고
    • Catalytic asymmetric cyclopropanation using bridged dirhodium tetraprolinates on solid support
    • Nagashima, T., Davies, H. M. L. (2002). Catalytic asymmetric cyclopropanation using bridged dirhodium tetraprolinates on solid support. Org. Lett., 4, 1989-1992.
    • (2002) Org. Lett , vol.4 , pp. 1989-1992
    • Nagashima, T.1    Davies, H.M.L.2
  • 32
    • 34548173218 scopus 로고    scopus 로고
    • Immobilized chiral ortho-metalated dirhodium(II) compounds as catalysts in the asymmetric cyclopropanation of styrene with ethyl diazoacetate
    • Lloret, J., Estevan, F., Bieger, K., Villanueva, C., Ubeda, M. A. (2007). Immobilized chiral ortho-metalated dirhodium(II) compounds as catalysts in the asymmetric cyclopropanation of styrene with ethyl diazoacetate. Organometallics, 26, 4145-4151.
    • (2007) Organometallics, , vol.26 , pp. 4145-4151
    • Lloret, J.1    Estevan, F.2    Bieger, K.3    Villanueva, C.4    Ubeda, M.A.5
  • 34
    • 0036811192 scopus 로고    scopus 로고
    • Enantioselective catalysis using heterogeneous bis(oxazoline) ligands: which factors infl uence the enantioselectivity? Chem
    • For a review of heterogeneous bis(oxazoline) ligands, see: Rechavi, D., Lemaire, M. (2002). Enantioselective catalysis using heterogeneous bis(oxazoline) ligands: which factors infl uence the enantioselectivity? Chem. Rev., 102, 3467-3494.
    • (2002) Rev., , vol.102 , pp. 3467-3494
    • Rechavi, D.1    Lemaire, M.2
  • 36
    • 0033407595 scopus 로고    scopus 로고
    • Enantioselective allylic alkylation using polymer-supported palladium catalysts
    • Hallman, K., Macedo, E., Nordström, K., Moberg, C. (1999). Enantioselective allylic alkylation using polymer-supported palladium catalysts. Tetrahedron Asymmetry, 10, 4037-4046.
    • (1999) Tetrahedron Asymmetry, , vol.10 , pp. 4037-4046
    • Hallman, K.1    Macedo, E.2    Nordström, K.3    Moberg, C.4
  • 37
    • 0036811245 scopus 로고    scopus 로고
    • Preparation of polymer-supported ligands and metal complexes for use in catalysis
    • Leadbeater, N. E., Marco, M. (2002). Preparation of polymer-supported ligands and metal complexes for use in catalysis. Chem. Rev., 102, 3217-3274.
    • (2002) Chem. Rev., , vol.102 , pp. 3217-3274
    • Leadbeater, N.E.1    Marco, M.2
  • 38
    • 0141619399 scopus 로고    scopus 로고
    • Polymer - supported organic catalysts
    • For relevant reviews, see: (a) Benaglia, M., Puglisi, A., Cozzi, F. (2003). Polymer - supported organic catalysts. Chem. Rev., 103, 3401-3429.
    • (2003) Chem. Rev , vol.103 , pp. 3401-3429
    • Benaglia, M.1    Puglisi, A.2    Cozzi, F.3
  • 39
    • 0009580654 scopus 로고
    • Asymmetric Robinson cyclization reaction catalyzed by polymer-bound l-proline
    • Kondo, K., Yamano, T., Takemoto, K. (1985). Asymmetric Robinson cyclization reaction catalyzed by polymer-bound l-proline. Makromol. Chem., 186, 1781-1785.
    • (1985) Makromol. Chem., , vol.186 , pp. 1781-1785
    • Kondo, K.1    Yamano, T.2    Takemoto, K.3
  • 40
    • 0000776283 scopus 로고    scopus 로고
    • Enantioselective aldol condensations catalyzed by poly(ethylene glycol)-supported proline
    • Benaglia, M., Celentano, G., Cozzi, F. (2001). Enantioselective aldol condensations catalyzed by poly(ethylene glycol)-supported proline. Adv. Synth. Catal., 343, 171-173.
    • (2001) Adv. Synth. Catal., , vol.343 , pp. 171-173
    • Benaglia, M.1    Celentano, G.2    Cozzi, F.3
  • 41
    • 33750070045 scopus 로고    scopus 로고
    • Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water
    • Font, D., Jimeno, C., Pericàs, M. A. (2006). Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water. Org. Lett., 8, 4653-4655.
    • (2006) Org. Lett., , vol.8 , pp. 4653-4655
    • Font, D.1    Jimeno, C.2    Pericàs, M.A.3
  • 43
    • 53849141478 scopus 로고    scopus 로고
    • Novel prolinamide-supported polystyrene as highly stereoselective and recyclable organocatalyst for the aldol reaction
    • Gruttadauria, M., Giacalone, F., Marculescu, A. M., Noto, R. (2008). Novel prolinamide-supported polystyrene as highly stereoselective and recyclable organocatalyst for the aldol reaction. Adv. Synth. Catal., 350, 1397-1405.
    • (2008) Adv. Synth. Catal., , vol.350 , pp. 1397-1405
    • Gruttadauria, M.1    Giacalone, F.2    Marculescu, A.M.3    Noto, R.4
  • 44
    • 73349125422 scopus 로고    scopus 로고
    • A highly selective, polymer-supported organocatalyst for the Michael additions with enzyme-like behavior
    • Alza, E., Pericàs, M. A. (2009). A highly selective, polymer-supported organocatalyst for the Michael additions with enzyme-like behavior. Adv. Synth. Catal., 351, 3051-3056.
    • (2009) Adv. Synth. Catal., , vol.351 , pp. 3051-3056
    • Alza, E.1    Pericàs, M.A.2
  • 45
    • 77950249530 scopus 로고    scopus 로고
    • Effi cient, enantioselective iminium catalysis with an immobilized, recyclable diarylprolinol silyl ether catalyst
    • Mager, I., Zeitler, K. (2010). Effi cient, enantioselective iminium catalysis with an immobilized, recyclable diarylprolinol silyl ether catalyst. Org. Lett., 12, 1480-1483.
    • (2010) Org. Lett., , vol.12 , pp. 1480-1483
    • Mager, I.1    Zeitler, K.2
  • 46
    • 0000779935 scopus 로고    scopus 로고
    • Poly(ethylene glycol)-supported chiral imidazolidin-4-one: an effi cient organic catalyst for the enantioselective Diels-Alder cycloaddition
    • Benaglia, M., Celentano, G., Cinquini, M., Puglisi, A., Cozzi, F. (2002). Poly(ethylene glycol)-supported chiral imidazolidin-4-one: an effi cient organic catalyst for the enantioselective Diels-Alder cycloaddition. Adv. Synth. Catal., 344, 149-152.
    • (2002) Adv. Synth. Catal., , vol.344 , pp. 149-152
    • Benaglia, M.1    Celentano, G.2    Cinquini, M.3    Puglisi, A.4    Cozzi, F.5
  • 47
    • 0344613309 scopus 로고    scopus 로고
    • Asymmetric organocatalytic Diels-Alder reactions on solid support
    • Selkäl ä, S. A., Tois, J., Pihko, P. M., Koskinen, A. M. P. (2002). Asymmetric organocatalytic Diels-Alder reactions on solid support. Adv. Synth. Catal., 344, 941-945.
    • (2002) Adv. Synth. Catal., , vol.344 , pp. 941-945
    • Selkälä, S.A.1    Tois, J.2    Pihko, P.M.3    Koskinen, A.M.P.4
  • 48
    • 26944476677 scopus 로고    scopus 로고
    • Nanostructured, solid - state organic, chiral Diels-Alder catalysts via acid-induced liquid crystal assembly
    • Pecinovsky, C. S., Nicodemus, G. D., Gin, D. L. (2005). Nanostructured, solid - state organic, chiral Diels-Alder catalysts via acid-induced liquid crystal assembly. Chem. Mater., 17, 4889-4891.
    • (2005) Chem. Mater., , vol.17 , pp. 4889-4891
    • Pecinovsky, C.S.1    Nicodemus, G.D.2    Gin, D.L.3
  • 49
    • 74049157760 scopus 로고    scopus 로고
    • Novel polymer-supported organocatalyst via ion exchange reaction: facile immobilization of chiral imidazolidin-4 - one and its application to Diels-Alder reaction
    • Haraguchi, N., Takemura, Y., Itsuno, S. (2010). Novel polymer-supported organocatalyst via ion exchange reaction: facile immobilization of chiral imidazolidin-4 - one and its application to Diels-Alder reaction. Tetrahedron Lett., 51, 1205-1208.
    • (2010) Tetrahedron Lett., , vol.51 , pp. 1205-1208
    • Haraguchi, N.1    Takemura, Y.2    Itsuno, S.3
  • 51
    • 0003554758 scopus 로고    scopus 로고
    • Schiff base catalysts for the asymmetric Strecker reaction identifi ed and optimized from parallel synthetic libraries
    • Sigman, M. S., Jacobsen, E. N. (1998). Schiff base catalysts for the asymmetric Strecker reaction identifi ed and optimized from parallel synthetic libraries. J. Am. Chem. Soc., 120, 4901-4902.
    • (1998) J. Am. Chem. Soc., , vol.120 , pp. 4901-4902
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 52
    • 0035969617 scopus 로고    scopus 로고
    • Highly enantioselective enone epoxidation catalyzed by short solid phase-bound peptides: dominant role of peptide helicity
    • Berkessel, A., Gasch, N., Glaubitz, K., Koch, C. (2001). Highly enantioselective enone epoxidation catalyzed by short solid phase-bound peptides: dominant role of peptide helicity. Org. Lett., 3, 3839-3842.
    • (2001) Org. Lett., , vol.3 , pp. 3839-3842
    • Berkessel, A.1    Gasch, N.2    Glaubitz, K.3    Koch, C.4
  • 54
    • 0001644876 scopus 로고
    • Polymer-bound Cinchona alkaloids as catalysts in the Michael reaction
    • Hermann, K., Wynberg, H. (1977). Polymer-bound Cinchona alkaloids as catalysts in the Michael reaction. Helv. Chim. Acta., 60, 2208-2212.
    • (1977) Helv. Chim. Acta., , vol.60 , pp. 2208-2212
    • Hermann, K.1    Wynberg, H.2
  • 55
    • 37049099702 scopus 로고
    • Michael reactions catalyzed by polymer-supported quaternary ammonium-salts derived from cinchona and ephedra alkaloids
    • Hodge, P., Khoshdel, E., Waterhouse, J. (1983). Michael reactions catalyzed by polymer-supported quaternary ammonium-salts derived from cinchona and ephedra alkaloids. J. Chem. Soc. Perkin Trans. 1, 2205-2209.
    • (1983) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2205-2209
    • Hodge, P.1    Khoshdel, E.2    Waterhouse, J.3
  • 56
    • 0032649829 scopus 로고    scopus 로고
    • Asymmetric synthesis of a-amino acids using polymer-supported chiral phase transfer catalysts
    • Zhengpu, Z., Yongmer, W., Zhen, W., Hodge, P. (1999). Asymmetric synthesis of a-amino acids using polymer-supported chiral phase transfer catalysts. React. Funct. Polym., 41, 37-43.
    • (1999) React. Funct. Polym , vol.41 , pp. 37-43
    • Zhengpu, Z.1    Yongmer, W.2    Zhen, W.3    Hodge, P.4
  • 57
    • 37049096554 scopus 로고
    • Michael additions catalysed by Cinchona alkaloids bound via their vinyl groups to preformed cross - linked polymers
    • Hodge, P., Khoshdel, E., Waterhouse, J., Fréchet, J. M. J. (1985). Michael additions catalysed by Cinchona alkaloids bound via their vinyl groups to preformed cross - linked polymers. J. Chem. Soc. Perkin Trans. 1, 2327-2331.
    • (1985) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2327-2331
    • Hodge, P.1    Khoshdel, E.2    Waterhouse, J.3    Fréchet, J.M.J.4
  • 59
    • 55049136453 scopus 로고    scopus 로고
    • Tailored polymer-supported templates in dynamic combinatorial libraries: simultaneous selection, amplifi cation and isolation of synthetic receptors
    • Besenius, P., Cormack, P. A. G., Liu, J., Otto, S., Sanders, J. K. M., Sherrington, D. C. (2008). Tailored polymer-supported templates in dynamic combinatorial libraries: simultaneous selection, amplifi cation and isolation of synthetic receptors. Chem. Eur. J., 14, 9006-9019.
    • (2008) Chem. Eur. J., , vol.14 , pp. 9006-9019
    • Besenius, P.1    Cormack, P.A.G.2    Liu, J.3    Otto, S.4    Sanders, J.K.M.5    Sherrington, D.C.6
  • 60
    • 84886007625 scopus 로고    scopus 로고
    • The Chemistry of Radical Polymerization, 2nd ed
    • For an introduction to free radical (co)polymerization, see ref. 6. See also: Moad, G., Solomon, D. H. (2006). The Chemistry of Radical Polymerization, 2nd ed. Elsevier, Oxford.
    • (2006) Elsevier, Oxford , vol.270 , pp. 717-732
    • Moad, G.1    Solomon, D.H.2
  • 63
    • 0034728145 scopus 로고    scopus 로고
    • Diam - BINAP"; a highly effi cient monomer for the synthesis of heterogeneous enantioselective catalysts
    • Halle, R. t., Colasson, B., Schulz, E., Spagnol, M., Lemaire, M. (2000). "Diam - BINAP"; a highly effi cient monomer for the synthesis of heterogeneous enantioselective catalysts. Tetrahedron Lett., 41, 643-646.
    • (2000) Tetrahedron Lett., , vol.41 , pp. 643-646
    • Halle, R.t.1    Colasson, B.2    Schulz, E.3    Spagnol, M.4    Lemaire, M.5
  • 64
    • 0034703269 scopus 로고    scopus 로고
    • A highly effective water-soluble polymer-supported catalyst for the two-phase asymmetric hydrogenation: preparation and use of a PEG-bound BINAP ligand
    • Fan, Q.-H., Deng, G.-J., Chen, X.-M., Xie, W.-C., Jiang, D.-Z., Liu, D.-S., Chan, A. S. C. (2000). A highly effective water-soluble polymer-supported catalyst for the two-phase asymmetric hydrogenation: preparation and use of a PEG-bound BINAP ligand. J. Mol. Catal. A Chem., 159, 37-43.
    • (2000) J. Mol. Catal. A Chem., , vol.159 , pp. 37-43
    • Fan, Q.-H.1    Deng, G.-J.2    Chen, X.-M.3    Xie, W.-C.4    Jiang, D.-Z.5    Liu, D.-S.6    Chan, A.S.C.7
  • 65
    • 0034635787 scopus 로고    scopus 로고
    • Synthesis of a rigid and optically active poly(BINAP) and its application in asymmetric catalysis
    • Yu, H.-B., Hu, Q.-S., Pu, L. (2000). Synthesis of a rigid and optically active poly(BINAP) and its application in asymmetric catalysis. Tetrahedron Lett., 41, 1681-1686.
    • (2000) Tetrahedron Lett., , vol.41 , pp. 1681-1686
    • Yu, H.-B.1    Hu, Q.-S.2    Pu, L.3
  • 66
    • 0028803963 scopus 로고
    • "Molecular imprinting effect" in the synthesis of immobilized rhodium complex catalyst (IRC cat)
    • Gamez, P., Dunjic, B., Pinel, C., Lemaire, M. (1995). "Molecular imprinting effect" in the synthesis of immobilized rhodium complex catalyst (IRC cat). Tetrahedron Lett., 36, 8779-8782.
    • (1995) Tetrahedron Lett., , vol.36 , pp. 8779-8782
    • Gamez, P.1    Dunjic, B.2    Pinel, C.3    Lemaire, M.4
  • 67
    • 0035794273 scopus 로고    scopus 로고
    • Enantiopure poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate): a new material for supported catalytic asymmetric hydrogen transfer reduction
    • Rolland, A., Hérault, D., Touchard, F., Saluzzo, C., Duval, R., Lemair, M. (2001). Enantiopure poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate): a new material for supported catalytic asymmetric hydrogen transfer reduction. Tetrahedron Asymmetry, 12, 811-815.
    • (2001) Tetrahedron Asymmetry, , vol.12 , pp. 811-815
    • Rolland, A.1    Hérault, D.2    Touchard, F.3    Saluzzo, C.4    Duval, R.5    Lemair, M.6
  • 68
    • 0027474658 scopus 로고
    • Polymer supported transition metal complexes for catalytic epoxidation of olefi ns
    • De, B. B., Lohray, B. B., Dhal, P. K. (1993). Polymer supported transition metal complexes for catalytic epoxidation of olefi ns. Tetrahedron Lett., 34, 2371-2374.
    • (1993) Tetrahedron Lett., , vol.34 , pp. 2371-2374
    • De, B.B.1    Lohray, B.B.2    Dhal, P.K.3
  • 69
    • 29544446558 scopus 로고    scopus 로고
    • Poly(styrene)-Supported Co-Salen Complexes as Effi cient Recyclable Catalysts for the Hydrolytic Kinetic Resolution of Epichlorohydrin
    • Zheng, X., Jones, C. W., Weck, M. (2006). Poly(styrene)-Supported Co-Salen Complexes as Effi cient Recyclable Catalysts for the Hydrolytic Kinetic Resolution of Epichlorohydrin. Chem. Eur. J., 12, 576-583.
    • (2006) Chem. Eur. J., , vol.12 , pp. 576-583
    • Zheng, X.1    Jones, C.W.2    Weck, M.3
  • 70
    • 77956914868 scopus 로고    scopus 로고
    • A polymer - supported chiral dirhodium(II) complex: highly durable and recyclable catalyst for asymmetric intramolecular CH insertion reactions
    • Takeda, K., Oohara, T., Anada, M., Nambu, H., Hashimoto, S. (2010). A polymer - supported chiral dirhodium(II) complex: highly durable and recyclable catalyst for asymmetric intramolecular CH insertion reactions. Angew. Chem. Int. Ed., 49, 6979-6983.
    • (2010) Angew. Chem. Int. Ed., , vol.49 , pp. 6979-6983
    • Takeda, K.1    Oohara, T.2    Anada, M.3    Nambu, H.4    Hashimoto, S.5
  • 71
    • 0001342326 scopus 로고    scopus 로고
    • Polymer-supported Bis(oxazoline)-copper complexes as catalysts in cyclopropanation reactions
    • Burguete, M. I., Fraile, J. M., Garcia, J. I., Garcia-Verdugo, E., Luis, S. V. (2000). Polymer-supported Bis(oxazoline)-copper complexes as catalysts in cyclopropanation reactions. Org. Lett., 2, 3905-3908.
    • (2000) Org. Lett., , vol.2 , pp. 3905-3908
    • Burguete, M.I.1    Fraile, J.M.2    Garcia, J.I.3    Garcia-Verdugo, E.4    Luis, S.V.5
  • 73
    • 0035796772 scopus 로고    scopus 로고
    • The aldol addition reaction: an old transformation at constant rebirth
    • Orlandi, S., Mandoli, A., Pini, D., Salvadori, P. (2001). The aldol addition reaction: an old transformation at constant rebirth. Angew. Chem. Int. Ed., 40, 2519-2521.
    • (2001) Angew. Chem. Int. Ed., , vol.40 , pp. 2519-2521
    • Orlandi, S.1    Mandoli, A.2    Pini, D.3    Salvadori, P.4
  • 75
    • 0001032779 scopus 로고
    • Functional polymers. 1. Poly(cinchona alkaloid-co-acrylonitrile)s. New polymer catalysts for asymmetric synthesis
    • Kobayashi, N., Iwai, K.(1978). Functional polymers. 1. Poly(cinchona alkaloid-co-acrylonitrile)s. New polymer catalysts for asymmetric synthesis. J. Am. Chem. Soc., 100, 7071-7072.
    • (1978) J. Am. Chem. Soc , vol.100 , pp. 7071-7072
    • Kobayashi, N.1    Iwai, K.2
  • 77
    • 0000711840 scopus 로고
    • A mechanistic insight leads to a greatly improved osmium-catalyzed asymmetric dihydroxylation process
    • Wai, J. S. M., Mark ó, I., Svendsen, J. S., Finn, M. G., Jacobsen, E. N., Sharpless, K. B. (1989). A mechanistic insight leads to a greatly improved osmium-catalyzed asymmetric dihydroxylation process. J. Am. Chem. Soc., 111, 1123-1125. Some other seminal publications are given in Reference [80]. [80] Kim, B. M., Sharpless, K. B. (1990). Heterogeneous catalytic asymmetric dihydroxylation: use of a polymer-bound alkaloid. Tetrahedron Lett., 31, 3003-3006.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 1123-1125
    • Wai, J.S.M.1    Markó, I.2    Svendsen, J.S.3    Finn, M.G.4    Jacobsen, E.N.5    Sharpless, K.B.6
  • 78
    • 0025908764 scopus 로고
    • Heterogeneous catalytic asymmetric dihydroxylation of olefi ns with the OsO 4 /Poly(9-O - Acylquinine-co-acrylonitrile) system
    • Pini, D., Petri, A., Nardi, A., Rosini, C., Salvadori, P. (1991). Heterogeneous catalytic asymmetric dihydroxylation of olefi ns with the OsO 4 /Poly(9-O - Acylquinine-co-acrylonitrile) system. Tetrahedron Lett., 32, 5175-5178.
    • (1991) Tetrahedron Lett., , vol.32 , pp. 5175-5178
    • Pini, D.1    Petri, A.2    Nardi, A.3    Rosini, C.4    Salvadori, P.5
  • 79
    • 0344269323 scopus 로고    scopus 로고
    • Polymer-supported bis-cinchona alkaloid ligands for asymmetric dihydroxylation of alkenes - a cautionary tale
    • Canali, L., Song, C. E., Sherrington, D. C. (1998). Polymer-supported bis-cinchona alkaloid ligands for asymmetric dihydroxylation of alkenes - a cautionary tale. Tetrahedron Asymmetry, 9, 1029-1034.
    • (1998) Tetrahedron Asymmetry , vol.9 , pp. 1029-1034
    • Canali, L.1    Song, C.E.2    Sherrington, D.C.3
  • 80
    • 58649121504 scopus 로고    scopus 로고
    • The selective O-acylation of hydroxyproline as a convenient method for the large-scale preparation of novel proline polymers and amphiphiles
    • Kristensen, T. E., Hansen, F. K., Hansen, T. (2009). The selective O-acylation of hydroxyproline as a convenient method for the large-scale preparation of novel proline polymers and amphiphiles. Eur. J. Org. Chem., 387-395.
    • (2009) Eur. J. Org. Chem , pp. 387-395
    • Kristensen, T.E.1    Hansen, F.K.2    Hansen, T.3
  • 81
    • 67650333080 scopus 로고    scopus 로고
    • Synthesis of Acrylic Polymer beads for solid-supported proline-derived organocatalysts
    • Kristensen, T. E., Vestli, K., Fredriksen, K. A., Hansen, F. K., Hansen, T. (2009). Synthesis of Acrylic Polymer beads for solid-supported proline-derived organocatalysts. Org. Lett., 11, 2968-2971.
    • (2009) Org. Lett , vol.11 , pp. 2968-2971
    • Kristensen, T.E.1    Vestli, K.2    Fredriksen, K.A.3    Hansen, F.K.4    Hansen, T.5
  • 82
    • 77949298192 scopus 로고    scopus 로고
    • A General approach for preparation of polymer-supported chiral organocatalysts via acrylic copolymerization
    • Kristensen, T. E., Vestli, K., Jakobsen, M. G., Hansen, F. K., Hansen, T. (2010). A General approach for preparation of polymer-supported chiral organocatalysts via acrylic copolymerization. J. Org. Chem., 75, 1620-1629.
    • (2010) J. Org. Chem , vol.75 , pp. 1620-1629
    • Kristensen, T.E.1    Vestli, K.2    Jakobsen, M.G.3    Hansen, F.K.4    Hansen, T.5
  • 83
    • 69249156564 scopus 로고    scopus 로고
    • New hydroxyproline based methacrylic polybetaines: synthesis, pH sensitivity and catalytic activity
    • Doyagüez, E. G., Parra, F., Corrales, G., Fernández-Mayoralas, A., Gallardo, A. (2009). New hydroxyproline based methacrylic polybetaines: synthesis, pH sensitivity and catalytic activity. Polymer, 50, 4438-4446.
    • (2009) Polymer , vol.50 , pp. 4438-4446
    • Doyagüez, E.G.1    Parra, F.2    Corrales, G.3    Fernández-Mayoralas, A.4    Gallardo, A.5
  • 84
    • 34547828826 scopus 로고    scopus 로고
    • Design of polymer nanofi ber systems for the immobilization of homogeneous catalysts - preparation and leaching studies
    • Stasiak, M., Röben, C., Rosenberger, N., Schleth, F., Studer, A., Greiner, A., Wendorff, J. H. (2007). Design of polymer nanofi ber systems for the immobilization of homogeneous catalysts - preparation and leaching studies. Polymer, 48, 5208-5218.
    • (2007) Polymer, , vol.48 , pp. 5208-5218
    • Stasiak, M.1    Röben, C.2    Rosenberger, N.3    Schleth, F.4    Studer, A.5    Greiner, A.6    Wendorff, J.H.7
  • 86
    • 50849092526 scopus 로고    scopus 로고
    • Asymmetric epoxidation, Michael addition, and triple cascade reaction using polymer-supported prolinol-based auxiliaries
    • Varela, M. C., Dixon, S. M., Lam, K. S., Schore, N. E. (2008). Asymmetric epoxidation, Michael addition, and triple cascade reaction using polymer-supported prolinol-based auxiliaries. T etrahedron, 64, 10087-10090.
    • (2008) T etrahedron, , vol.64 , pp. 10087-10090
    • Varela, M.C.1    Dixon, S.M.2    Lam, K.S.3    Schore, N.E.4
  • 87
    • 0037111596 scopus 로고    scopus 로고
    • Oxazaborolidines as functional monomers: ketone reduction using polymer-supported Corey, Bakshi, and Shibata catalysts
    • Price, M. D., Sui, J. K., Kurth, M. J., Schore, N. E. (2002). Oxazaborolidines as functional monomers: ketone reduction using polymer-supported Corey, Bakshi, and Shibata catalysts. J. Org. Chem., 67, 8086-8089.
    • (2002) J. Org. Chem., , vol.67 , pp. 8086-8089
    • Price, M.D.1    Sui, J.K.2    Kurth, M.J.3    Schore, N.E.4
  • 88
    • 48549086083 scopus 로고    scopus 로고
    • Immobilization of oligostyrene-prolinol conjugates into polystyrene via electrospinning and applications of these fi bers in catalysis
    • Röben, C., Stasiak, M., Janza, B., Greiner, A., Wendorff, J. H., Studer, A. (2008). Immobilization of oligostyrene-prolinol conjugates into polystyrene via electrospinning and applications of these fi bers in catalysis. Synthesis, 2163-2168.
    • (2008) Synthesis, , pp. 2163-2168
    • Röben, C.1    Stasiak, M.2    Janza, B.3    Greiner, A.4    Wendorff, J.H.5    Studer, A.6
  • 89
    • 0037111596 scopus 로고    scopus 로고
    • Oxazaborolidines as functional monomers: ketone reduction using polymer-supported Corey, Bakshi, and Shibata catalysts
    • Price, M. D., Sui, J. K., Kurth, M. J., Schore, N. E. (2002). Oxazaborolidines as functional monomers: ketone reduction using polymer-supported Corey, Bakshi, and Shibata catalysts. J. Org. Chem., 67, 8086-8089.
    • (2002) J. Org. Chem., , vol.67 , pp. 8086-8089
    • Price, M.D.1    Sui, J.K.2    Kurth, M.J.3    Schore, N.E.4
  • 90
    • 0028214648 scopus 로고
    • Polymer-supported chiral Lewis acids as asymmetric catalysts for diels-alder reactions of methacrolein with cyclopentadiene
    • Watanabe, K., Koizumi, T., Ito, K. (1994). Polymer-supported chiral Lewis acids as asymmetric catalysts for diels-alder reactions of methacrolein with cyclopentadiene . Tetrahedron Asymmetry, 5, 523-526.
    • (1994) Tetrahedron Asymmetry, , vol.5 , pp. 523-526
    • Watanabe, K.1    Koizumi, T.2    Ito, K.3
  • 91
    • 77955258985 scopus 로고    scopus 로고
    • Organocatalytic tuneable amino acid polymers prepared by controlled radical polymerization
    • Evans , A. C. , Lu , A. , Ondeck , C. , Longbottom , D. A. , O'Reilly , R. K. ( 2010 ). Organocatalytic tuneable amino acid polymers prepared by controlled radical polymerization . Macromolecules , 43 , 6374-6380 .
    • (2010) Macromolecules , vol.43 , pp. 6374-6380
    • Evans, A.C.1    Lu, A.2    Ondeck, C.3    Longbottom, D.A.4    O'Reilly, R.K.5
  • 92
    • 0030924999 scopus 로고    scopus 로고
    • A polymer - enlarged homogeneously soluble oxazaborolidine catalyst for the asymmetric reduction of ketones by borane
    • Felder , M. , Giffels , G. , Wandrey , C. ( 1997 ). A polymer - enlarged homogeneously soluble oxazaborolidine catalyst for the asymmetric reduction of ketones by borane . Tetrahedron Asymmetry , 8 , 1975-1977.
    • (1997) Tetrahedron Asymmetry , vol.8 , pp. 1975-1977
    • Felder, M.1    Giffels, G.2    Wandrey, C.3
  • 93
    • 0000257568 scopus 로고    scopus 로고
    • Immobilization of chiral ligands on polymer fi bers by electron beam induced grafting and applications in enantioselective catalysis
    • Degni , S. , Wilén , C. - E. , Leino , R. ( 2001 ). Immobilization of chiral ligands on polymer fi bers by electron beam induced grafting and applications in enantioselective catalysis . Org. Lett. , 3 , 2551-2554.
    • (2001) Org. Lett , vol.3 , pp. 2551-2554
    • Degni, S.1    Wilén, C.-E.2    Leino, R.3
  • 94
    • 33947219450 scopus 로고    scopus 로고
    • Comparison of enantioselective reductions using bead and monolith " disk " polymer formulations of CBS catalysts
    • Varela , M. C. , Dixon , S. M. , Price , M. D. , Merit, J. E. , Berget, P. E. , Shiraki, S. , Kurth, M. J. , Schore , N. E. ( 2007 ). Comparison of enantioselective reductions using bead and monolith " disk " polymer formulations of CBS catalysts . Tetrahedron , 63 , 3334-3339 .
    • (2007) Tetrahedron , vol.63 , pp. 3334-3339
    • Varela, M.C.1    Dixon, S.M.2    Price, M.D.3    Merit, J.E.4    Berget, P.E.5    Shiraki, S.6    Kurth, M.J.7    Schore, N.E.8
  • 95
    • 0035533042 scopus 로고    scopus 로고
    • The chemzyme membrane reactor in the fi ne chemicals industry
    • Wöltinger , J. , Bommarius , A. S. , Drauz , K. , Wandrey , C. ( 2001 ). The chemzyme membrane reactor in the fi ne chemicals industry . Org. Proc. Res. Dev. , 5 , 241-248.
    • (2001) Org. Proc. Res. Dev , vol.5 , pp. 241-248
    • Wöltinger, J.1    Bommarius, A.S.2    Drauz, K.3    Wandrey, C.4
  • 96
    • 0141749236 scopus 로고    scopus 로고
    • Towards more chemically robust polymer - supported chiral catalysts: a , a - diphenyl - L - prolinol based catalysts for the reduction of prochiral ketones with borane
    • Kell , R. J. , Hodge , P. , Snedden , P. , Watson , D. ( 2003 ). Towards more chemically robust polymer - supported chiral catalysts: a , a - diphenyl - L - prolinol based catalysts for the reduction of prochiral ketones with borane . Org. Biomol. Chem. , 1 , 3238-3243 .
    • (2003) Org. Biomol. Chem , vol.1 , pp. 3238-3243
    • Kell, R.J.1    Hodge, P.2    Snedden, P.3    Watson, D.4
  • 97
    • 77149179738 scopus 로고    scopus 로고
    • Synthesis and application of polymer-supported chiral Br ø nsted acid organocatalysts
    • Rueping, M., Sugiono, E., Steck, A., Theissmann, T. (2010). Synthesis and application of polymer-supported chiral Br ø nsted acid organocatalysts. Adv. Synth. Catal., 352, 281-287.
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 281-287
    • Rueping, M.1    Sugiono, E.2    Steck, A.3    Theissmann, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.