메뉴 건너뛰기




Volumn , Issue , 2011, Pages 291-321

Catalysis with Chirally Modified Metal Surfaces: Scope and Mechanisms

Author keywords

Catalysis, chirally modified metal surfaces enantioselective catalysis, amplification; Chirally modified metal surfaces ketone and C 63742; C double bond asymmetric hydrogenation; Scope of catalysis, chirally modified metals, Pt, Pd, Ni, Rh, Ir metals cinchona alkaloids

Indexed keywords


EID: 84885989065     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118087992.ch6     Document Type: Chapter
Times cited : (3)

References (210)
  • 2
    • 1842631437 scopus 로고    scopus 로고
    • Asymmetric catalysis: an enabling science
    • Trost, B. M. (2004). Asymmetric catalysis: an enabling science. Proc. Natl. Acad. Sci. U.S.A., 101, 5348-5355.
    • (2004) Proc. Natl. Acad. Sci. U.S.A., , vol.101 , pp. 5348-5355
    • Trost, B.M.1
  • 5
    • 36849062625 scopus 로고    scopus 로고
    • Asymmetric catalysis at chiral metal surfaces
    • Mallat, T., Orglmeister, E., Baiker, A. (2007). Asymmetric catalysis at chiral metal surfaces. Chem. Rev., 107, 4863-4890.
    • (2007) Chem. Rev., , vol.107 , pp. 4863-4890
    • Mallat, T.1    Orglmeister, E.2    Baiker, A.3
  • 8
    • 84906377691 scopus 로고
    • Asymmetric hydrogenation of methyl benzoylformate using platinum-carbon catalysts modified with cinchonidine
    • Orito, Y., Imai, S., Niwa, S., Nguyen, G. H. (1979). Asymmetric hydrogenation of methyl benzoylformate using platinum-carbon catalysts modified with cinchonidine . J. Syn. Org. Chem. Jpn., 37, 173-174.
    • (1979) J. Syn. Org. Chem. Jpn., , vol.37 , pp. 173-174
    • Orito, Y.1    Imai, S.2    Niwa, S.3    Nguyen, G.H.4
  • 10
    • 33748552702 scopus 로고    scopus 로고
    • Heterogeneous catalytic enantioselective hydrogenation of activated ketones
    • Bartók, M. (2006). Heterogeneous catalytic enantioselective hydrogenation of activated ketones. Curr. Org. Chem., 10, 1533-1567.
    • (2006) Curr. Org. Chem., , vol.10 , pp. 1533-1567
    • Bartók, M.1
  • 11
    • 20444375094 scopus 로고    scopus 로고
    • Asymmetric heterogeneous catalysis: science and engineering
    • Murzin, D. Y., Maki-Arvela, P., Toukoniitty, E., Salmi, T. (2005). Asymmetric heterogeneous catalysis: science and engineering. Catal. Rev., 47, 175-256.
    • (2005) Catal. Rev., , vol.47 , pp. 175-256
    • Murzin, D.Y.1    Maki-Arvela, P.2    Toukoniitty, E.3    Salmi, T.4
  • 12
    • 0038646248 scopus 로고    scopus 로고
    • Enantioselective hydrogenation using heterogeneous modified catalysts: an update
    • Studer, M., Blaser, H. U., Exner, C. (2003). Enantioselective hydrogenation using heterogeneous modified catalysts: an update. Adv. Synth. Catal., 345, 45-65.
    • (2003) Adv. Synth. Catal., , vol.345 , pp. 45-65
    • Studer, M.1    Blaser, H.U.2    Exner, C.3
  • 14
    • 0037200218 scopus 로고    scopus 로고
    • Continuous hydrogenation of 1-phenyl-1,2-propanedione under transient and steady-state conditions: regioselectivity, enantio selectivity and catalyst deactivation
    • Toukoniitty, E., Maki-Arvela, P., Neyestanaki, A. K., Salmi, T., Murzin, D. Y. (2002). Continuous hydrogenation of 1-phenyl-1,2-propanedione under transient and steady-state conditions: regioselectivity, enantio selectivity and catalyst deactivation . A ppl. Catal. A, 235, 125-138.
    • (2002) A ppl. Catal. A, , vol.235 , pp. 125-138
    • Toukoniitty, E.1    Maki-Arvela, P.2    Neyestanaki, A.K.3    Salmi, T.4    Murzin, D.Y.5
  • 15
    • 0001054290 scopus 로고
    • Chiral nitrogen-compounds as new modifiers for the enantioselective hydrogenation of ethyl pyruvate
    • Minder, B., Schürch, M., Mallat, T., Baiker, A. (1995). Chiral nitrogen-compounds as new modifiers for the enantioselective hydrogenation of ethyl pyruvate. Catal. Lett., 31, 143-151.
    • (1995) Catal. Lett., , vol.31 , pp. 143-151
    • Minder, B.1    Schürch, M.2    Mallat, T.3    Baiker, A.4
  • 16
    • 17044428905 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of ethyl pyruvate catalyzed by alumina support rhodium modified with quinine
    • Xiong, W., Ma, H. X., Hong, Y. Y., Chen, H., Li, X. J. (2005). Enantioselective hydrogenation of ethyl pyruvate catalyzed by alumina support rhodium modified with quinine. Tetrahedron Asymmetry, 16, 1449-1452.
    • (2005) Tetrahedron Asymmetry, , vol.16 , pp. 1449-1452
    • Xiong, W.1    Ma, H.X.2    Hong, Y.Y.3    Chen, H.4    Li, X.J.5
  • 18
    • 0035858709 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of ethyl pyruvate catalyzed by PVP-stabilized rhodium nanoclusters
    • Huang, Y. L., Chen, J. R., Chen, H., Li, R. X., Li, Y. Z., Min, L. E., Li, X. J. (2001). Enantioselective hydrogenation of ethyl pyruvate catalyzed by PVP-stabilized rhodium nanoclusters. J. Mol. Catal. A Chem., 170, 143-146.
    • (2001) J. Mol. Catal. A Chem., , vol.170 , pp. 143-146
    • Huang, Y.L.1    Chen, J.R.2    Chen, H.3    Li, R.X.4    Li, Y.Z.5    Min, L.E.6    Li, X.J.7
  • 19
    • 0037168413 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of ethyl pyruvate catalyzed by polyvinylpyrrolidone-stabilized and supported rhodium nanocluster
    • Huang, Y. L., Li, Y. Z., Hu, J. Y., Cheng, P. M., Chen, H., Li, R. X., Li, X. J., Yip, C. W., Chan, A. S. C. (2002). Enantioselective hydrogenation of ethyl pyruvate catalyzed by polyvinylpyrrolidone-stabilized and supported rhodium nanocluster . J. Mol. Catal. A Chem., 189, 219-224.
    • (2002) J. Mol. Catal. A Chem., , vol.189 , pp. 219-224
    • Huang, Y.L.1    Li, Y.Z.2    Hu, J.Y.3    Cheng, P.M.4    Chen, H.5    Li, R.X.6    Li, X.J.7    Yip, C.W.8    Chan, A.S.C.9
  • 20
    • 0037374788 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of ethyl pyruvate catalyzed by TS-1 supported rhodium nanoclusters
    • Ma, H. X., Chen, H., Zhang, Q., Li, X. J. (2003). Enantioselective hydrogenation of ethyl pyruvate catalyzed by TS-1 supported rhodium nanoclusters. J. Mol. Catal. A Chem., 196, 131-135.
    • (2003) J. Mol. Catal. A Chem., , vol.196 , pp. 131-135
    • Ma, H.X.1    Chen, H.2    Zhang, Q.3    Li, X.J.4
  • 22
    • 27744455932 scopus 로고    scopus 로고
    • Rhodium-catalyzed enantioselective hydrogenation of ketopantolactone
    • Maris, M., Mallat, T., Baiker, A. (2005). Rhodium-catalyzed enantioselective hydrogenation of ketopantolactone. J. Mol. Catal. A Chem., 242, 151-155.
    • (2005) J. Mol. Catal. A Chem., , vol.242 , pp. 151-155
    • Maris, M.1    Mallat, T.2    Baiker, A.3
  • 23
    • 30144445311 scopus 로고    scopus 로고
    • Why are alpha - hydroxycarboxylic acids poor chiral modifiers for Pt in the hydrogenation of ketones? J
    • Maris, M., Ferri, D., Konigsmann, L., Mallat, T., Baiker, A. (2006). Why are alpha - hydroxycarboxylic acids poor chiral modifiers for Pt in the hydrogenation of ketones? J. Catal., 237, 230-236.
    • (2006) Catal., , vol.237 , pp. 230-236
    • Maris, M.1    Ferri, D.2    Konigsmann, L.3    Mallat, T.4    Baiker, A.5
  • 24
    • 37049068411 scopus 로고
    • Carbonyl cluster derived polystyrene supported platinum for asymmetric hydrogenation of alpha - ketoesters
    • Bhaduri, S., Darshane, V. S., Sharma, K., Mukesh, D. (1992). Carbonyl cluster derived polystyrene supported platinum for asymmetric hydrogenation of alpha - ketoesters. J. Chem. Soc. Chem. Comm., 1738-1740.
    • (1992) J. Chem. Soc. Chem. Comm., , pp. 1738-1740
    • Bhaduri, S.1    Darshane, V.S.2    Sharma, K.3    Mukesh, D.4
  • 27
    • 0011489282 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of carbonyl compounds over Pd-Pt/alumina catalysts
    • Mallat, T., Szabo, S., Schurch, M., Gobel, U. W., Baiker, A. (1997). Enantioselective hydrogenation of carbonyl compounds over Pd-Pt/alumina catalysts. Catal. Lett., 47, 221-227.
    • (1997) Catal. Lett., , vol.47 , pp. 221-227
    • Mallat, T.1    Szabo, S.2    Schurch, M.3    Gobel, U.W.4    Baiker, A.5
  • 29
    • 0033589349 scopus 로고    scopus 로고
    • Preparation and characterisation of solvent-stabilised nanoparticulate platinum and palladium and their catalytic behaviour towards the enantioselective hydrogenation of ethyl pyruvate
    • Collier, P. J., Iggo, J. A., Whyman, R. (1999). Preparation and characterisation of solvent-stabilised nanoparticulate platinum and palladium and their catalytic behaviour towards the enantioselective hydrogenation of ethyl pyruvate. J. Mol. Catal. A Chem., 146, 149-157.
    • (1999) J. Mol. Catal. A Chem., , vol.146 , pp. 149-157
    • Collier, P.J.1    Iggo, J.A.2    Whyman, R.3
  • 30
    • 0038175037 scopus 로고    scopus 로고
    • Solvent and support effects in enantioselective hydrogenation of isophorone with (S)-alpha,alpha-diphenyl-2 - pyrrolidinemethanol modified palladium
    • Sipos, E., Tungler, A., Bitter, I. (2003). Solvent and support effects in enantioselective hydrogenation of isophorone with (S)-alpha,alpha-diphenyl-2 - pyrrolidinemethanol modified palladium. React. Kinet. Catal. Lett., 79, 101-109.
    • (2003) React. Kinet. Catal. Lett., , vol.79 , pp. 101-109
    • Sipos, E.1    Tungler, A.2    Bitter, I.3
  • 32
    • 0033579201 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of methyl pyruvate over polymer-stabilized and supported iridium clusters
    • Zuo, X. B., Liu, H. F., Yue, C. (1999). Enantioselective hydrogenation of methyl pyruvate over polymer-stabilized and supported iridium clusters. J. Mol. Catal. A Chem., 147, 63-72.
    • (1999) J. Mol. Catal. A Chem., , vol.147 , pp. 63-72
    • Zuo, X.B.1    Liu, H.F.2    Yue, C.3
  • 33
    • 26844549565 scopus 로고    scopus 로고
    • Iridium-supported catalyst for enantioselective hydrogenation of 1-phenyl-1,2-propanedione: the effects of the addition of promoter and the modifier concentration
    • Marzialetti, T., Fierro, J. L. G., Reyes, P. (2005). Iridium-supported catalyst for enantioselective hydrogenation of 1-phenyl-1,2-propanedione: the effects of the addition of promoter and the modifier concentration. Catal. Today., 107-108, 235-243.
    • (2005) Catal. Today., 107-108, , pp. 235-243
    • Marzialetti, T.1    Fierro, J.L.G.2    Reyes, P.3
  • 34
    • 0042893463 scopus 로고    scopus 로고
    • Non-linear effect of modifier composition on enantioselectivity in asymmetric hydrogenation over platinum metals
    • Huck, W. M., Mallat, T., Baiker, A. (2003). Non-linear effect of modifier composition on enantioselectivity in asymmetric hydrogenation over platinum metals. Adv. Synth. Catal., 345, 255-260.
    • (2003) Adv. Synth. Catal., , vol.345 , pp. 255-260
    • Huck, W.M.1    Mallat, T.2    Baiker, A.3
  • 35
    • 0033606243 scopus 로고    scopus 로고
    • Highly enantioselective heterogeneously catalyzed hydrogenation of alpha-ketoesters under mild conditions
    • LeBlond, C., Wang, J., Liu, J., Andrews, A. T., Sun, Y. K. (1999). Highly enantioselective heterogeneously catalyzed hydrogenation of alpha-ketoesters under mild conditions. J. Am. Chem. Soc., 121, 4920-4921.
    • (1999) J. Am. Chem. Soc., , vol.121 , pp. 4920-4921
    • LeBlond, C.1    Wang, J.2    Liu, J.3    Andrews, A.T.4    Sun, Y.K.5
  • 36
    • 33744813511 scopus 로고    scopus 로고
    • Study of enantioselective hydrogenation of bulky esters of phenylglyoxylic acid on Pt-CD and Pt-beta-ICN chiral catalysts: steric effect of ester groups and inversion of enantio selectivity
    • Szöri, K., Balàzsik, K., Felföldi, K., Bartók, M. (2006). Study of enantioselective hydrogenation of bulky esters of phenylglyoxylic acid on Pt-CD and Pt-beta-ICN chiral catalysts: steric effect of ester groups and inversion of enantio selectivity. J. Catal., 241, 149-154.
    • (2006) J. Catal., , vol.241 , pp. 149-154
    • Szöri, K.1    Balàzsik, K.2    Felföldi, K.3    Bartók, M.4
  • 37
    • 0001454084 scopus 로고    scopus 로고
    • Enantioselective Catalysts and Reactions. In: G. Ertl, H. Knözinger, J. Weitkamp (Eds.) Handbook of Heterogeneous Catalysis
    • VCH, Weinheim, Germany
    • Baiker, A., Blaser, H. U. (1997). Enantioselective Catalysts and Reactions. In: G. Ertl, H. Knözinger, J. Weitkamp (Eds.) Handbook of Heterogeneous Catalysis. VCH, Weinheim, Germany, p. 2422.
    • (1997) , pp. 2422
    • Baiker, A.1    Blaser, H.U.2
  • 38
    • 0032473808 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of alpha - ketoesters over finely dispersed polymer-stabilized platinum clusters
    • Zuo, X. B., Liu, H. F., Liu, M. H. (1998). Asymmetric hydrogenation of alpha - ketoesters over finely dispersed polymer-stabilized platinum clusters. Tetrahedron Lett., 39, 1941-1944.
    • (1998) Tetrahedron Lett., , vol.39 , pp. 1941-1944
    • Zuo, X.B.1    Liu, H.F.2    Liu, M.H.3
  • 39
    • 0034616023 scopus 로고    scopus 로고
    • Asymmetric synthesis of alkyl 5-oxotetrahydrofuran-2-carboxylates by enantioselective hydrogenation of dialkyl 2-oxoglutarates over cinchona modified Pt/Al 2 O 3 catalysts
    • Balàzsik, K., Szöri, K., Felföldi, K., Törok, B., Bartók, M. (2000). Asymmetric synthesis of alkyl 5-oxotetrahydrofuran-2-carboxylates by enantioselective hydrogenation of dialkyl 2-oxoglutarates over cinchona modified Pt/Al 2 O 3 catalysts . Chem. Commun., 555-556.
    • (2000) Chem. Commun., , pp. 555-556
    • Balàzsik, K.1    Szöri, K.2    Felföldi, K.3    Törok, B.4    Bartók, M.5
  • 43
    • 33645891197 scopus 로고    scopus 로고
    • Steric and electronic effects in the enantioselective hydrogenation of activated ketones on platinum: directing effect of ester group
    • Diezi, S., Reimann, S., Bonalumi, N., Mallat, T., Baiker, A. (2006). Steric and electronic effects in the enantioselective hydrogenation of activated ketones on platinum: directing effect of ester group. J. Catal., 239, 255-262.
    • (2006) J. Catal., , vol.239 , pp. 255-262
    • Diezi, S.1    Reimann, S.2    Bonalumi, N.3    Mallat, T.4    Baiker, A.5
  • 45
    • 20444466430 scopus 로고    scopus 로고
    • Competition at chiral metal surfaces: fundamental aspects of the inversion of enantioselectivity in hydrogenations on platinum
    • Bonalumi, N., Vargas, A., Ferri, D., Burgi, T., Mallat, T., Baiker, A. (2005). Competition at chiral metal surfaces: fundamental aspects of the inversion of enantioselectivity in hydrogenations on platinum. J. Am. Chem. Soc., 127, 8467-8477.
    • (2005) J. Am. Chem. Soc., , vol.127 , pp. 8467-8477
    • Bonalumi, N.1    Vargas, A.2    Ferri, D.3    Burgi, T.4    Mallat, T.5    Baiker, A.6
  • 47
    • 0742272559 scopus 로고    scopus 로고
    • 1-Naphthyl-1,2-ethanediol as a new chiral modifier of platinum in the enantio selective hydrogenation of activated ketones
    • Marinas, A., Mallat, T., Baiker, A. (2004). 1-Naphthyl-1,2-ethanediol as a new chiral modifier of platinum in the enantio selective hydrogenation of activated ketones. J. Catal., 221, 666-669.
    • (2004) J. Catal., , vol.221 , pp. 666-669
    • Marinas, A.1    Mallat, T.2    Baiker, A.3
  • 48
    • 22144471911 scopus 로고    scopus 로고
    • Quaternary ammonium derivatives of cinchonidine as new chiral modifiers for platinum
    • Orglmeister, E., Mallat, T., Baiker, A. (2005). Quaternary ammonium derivatives of cinchonidine as new chiral modifiers for platinum. J. Catal., 233, 333-341.
    • (2005) J. Catal., , vol.233 , pp. 333-341
    • Orglmeister, E.1    Mallat, T.2    Baiker, A.3
  • 49
    • 69549133717 scopus 로고    scopus 로고
    • Fundamental aspects of the chiral modification of platinum with peptides: asymmetric induction in hydrogenation of activated ketones
    • Mondelli, C., Vargas, A., Santarossa, G., Baiker, A. (2009). Fundamental aspects of the chiral modification of platinum with peptides: asymmetric induction in hydrogenation of activated ketones. J. Phys. Chem. C, 113, 15246-15259.
    • (2009) J. Phys. Chem. C, , vol.113 , pp. 15246-15259
    • Mondelli, C.1    Vargas, A.2    Santarossa, G.3    Baiker, A.4
  • 54
    • 0042838183 scopus 로고    scopus 로고
    • Towards a molecular understanding of asymmetric heterogeneous catalysis: hydrogenation of 1-phenyl-1,2-propanedione
    • Toukoniitty, E., Maki-Arvela, P., Nieminen, V., Salmi, T., Murzin, D. Y. (2003). Towards a molecular understanding of asymmetric heterogeneous catalysis: hydrogenation of 1-phenyl-1,2-propanedione. Kinet. Catal., 44, 562-571.
    • (2003) Kinet. Catal., , vol.44 , pp. 562-571
    • Toukoniitty, E.1    Maki-Arvela, P.2    Nieminen, V.3    Salmi, T.4    Murzin, D.Y.5
  • 55
    • 0141678116 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of cyclohexane-1,2-dione over cinchonidine-modified platinum
    • Sonderegger, O. J., Bürgi, T., Baiker, A. (2003). Asymmetric hydrogenation of cyclohexane-1,2-dione over cinchonidine-modified platinum. J. Catal., 215, 116-121.
    • (2003) J. Catal., , vol.215 , pp. 116-121
    • Sonderegger, O.J.1    Bürgi, T.2    Baiker, A.3
  • 56
    • 0002206025 scopus 로고    scopus 로고
    • Hydrogenation of butane-2,3-dione with heterogeneous cinchona modified platinum catalysts: a combination of an enantioselective reaction and kinetic resolution
    • Studer, M., Okafor, V., Blaser, H. U. (1998). Hydrogenation of butane-2,3-dione with heterogeneous cinchona modified platinum catalysts: a combination of an enantioselective reaction and kinetic resolution. Chem. Commun., 1053-1054.
    • (1998) Chem. Commun., , pp. 1053-1054
    • Studer, M.1    Okafor, V.2    Blaser, H.U.3
  • 57
    • 0037039049 scopus 로고    scopus 로고
    • Hydrosilylation of cinchonidine and 9-O-TMS-cinchonidine with triethoxysilane: application of 11-(triethoxysilyl) - 10,11-dihydrocinchonidine as a chiral modifier in the enantioselective hydrogenation of 1-phenylpropane-1,2-dione
    • Lindholm, A., Maki-Arvela, P., Toukoniitty, E., Pakkanen, T. A., Hirvi, J. T., Salmi, T., Murzin, D. Y., Sjoholm, R., Leino, R. (2002). Hydrosilylation of cinchonidine and 9-O-TMS-cinchonidine with triethoxysilane: application of 11-(triethoxysilyl) - 10,11-dihydrocinchonidine as a chiral modifier in the enantioselective hydrogenation of 1-phenylpropane-1,2-dione. J. Chem. Soc. Perk. Trans. 1, 2605-2612.
    • (2002) J. Chem. Soc. Perk. Trans. , vol.1 , pp. 2605-2612
    • Lindholm, A.1    Maki-Arvela, P.2    Toukoniitty, E.3    Pakkanen, T.A.4    Hirvi, J.T.5    Salmi, T.6    Murzin, D.Y.7    Sjoholm, R.8    Leino, R.9
  • 58
    • 21844433201 scopus 로고    scopus 로고
    • Effect of modifier structure in asymmetric 1-phenylpropane-1,2-dione hydrogenation
    • Busygin, I., Toukoniitty, E., Leino, R., Murzin, D. Y. (2005). Effect of modifier structure in asymmetric 1-phenylpropane-1,2-dione hydrogenation. J. Mol. Catal. A Chem., 236, 227-238.
    • (2005) J. Mol. Catal. A Chem., , vol.236 , pp. 227-238
    • Busygin, I.1    Toukoniitty, E.2    Leino, R.3    Murzin, D.Y.4
  • 59
    • 0030810409 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of alpha-ketoamides over Pt/Al 2 O 3 modified by cinchona alkaloids
    • Wang, G. Z., Mallat, T., Baiker, A. (1997). Enantioselective hydrogenation of alpha-ketoamides over Pt/Al 2 O 3 modified by cinchona alkaloids. Tetrahedron Asymmetry, 8, 2133-2140.
    • (1997) Tetrahedron Asymmetry, , vol.8 , pp. 2133-2140
    • Wang, G.Z.1    Mallat, T.2    Baiker, A.3
  • 60
    • 4143105564 scopus 로고    scopus 로고
    • Synthesis of substituted mandelic acid derivatives via enantioselective hydrogenation: homogeneous versus heterogeneous catalysis
    • Cederbaum, F., Lamberth, C., Malan, C., Naud, F., Spindler, F., Studer, M., Blaser, H. U. (2004). Synthesis of substituted mandelic acid derivatives via enantioselective hydrogenation: homogeneous versus heterogeneous catalysis. Adv. Synth. Catal., 346, 842-848.
    • (2004) Adv. Synth. Catal., , vol.346 , pp. 842-848
    • Cederbaum, F.1    Lamberth, C.2    Malan, C.3    Naud, F.4    Spindler, F.5    Studer, M.6    Blaser, H.U.7
  • 61
    • 2542446237 scopus 로고    scopus 로고
    • Enantio selective reduction of isatin derivatives over cinchonidine modified Pt/alumina
    • Sonderegger, O. J., Bürgi, T., Limbach, L. K., Baiker, A. (2004). Enantio selective reduction of isatin derivatives over cinchonidine modified Pt/alumina. J. Mol. Catal. A Chem., 217, 93-101.
    • (2004) J. Mol. Catal. A Chem., , vol.217 , pp. 93-101
    • Sonderegger, O.J.1    Bürgi, T.2    Limbach, L.K.3    Baiker, A.4
  • 62
    • 0001773345 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of a cyclic imidoketone over chirally modified Pt/Al 2 O 3
    • Künzle, N., Szabo, A., Schürch, M., Wang, G. Z., Mallat, T., Baiker, A. (1998). Enantioselective hydrogenation of a cyclic imidoketone over chirally modified Pt/Al 2 O 3. Chem. Commun., 1377-1378.
    • (1998) Chem. Commun., , pp. 1377-1378
    • Künzle, N.1    Szabo, A.2    Schürch, M.3    Wang, G.Z.4    Mallat, T.5    Baiker, A.6
  • 63
    • 0039528130 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of pyrrolidine-2,3,5-triones over the Pt-cinchonidine system
    • Szabo, A., Kunzle, N., Mallat, T., Baiker, A. (1999). Enantioselective hydrogenation of pyrrolidine-2,3,5-triones over the Pt-cinchonidine system. Tetrahedron Asymmetry, 10, 61-76.
    • (1999) Tetrahedron Asymmetry, , vol.10 , pp. 61-76
    • Szabo, A.1    Kunzle, N.2    Mallat, T.3    Baiker, A.4
  • 64
    • 0038373943 scopus 로고    scopus 로고
    • New synthesis of a useful C3 chiral building block by a heterogeneous method: enantioselective hydrogenation of pyruvaldehyde dimethyl acetal over cinchona modified Pt/Al 2 O 3 catalysts
    • Török, B., Felföldi, K., Balàzsik, K., Bartók, M. (1999). New synthesis of a useful C3 chiral building block by a heterogeneous method: enantioselective hydrogenation of pyruvaldehyde dimethyl acetal over cinchona modified Pt/Al 2 O 3 catalysts . Chem. Commun., 1725-1726.
    • (1999) Chem. Commun., , pp. 1725-1726
    • Török, B.1    Felföldi, K.2    Balàzsik, K.3    Bartók, M.4
  • 65
    • 0033533541 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of alpha-keto acetals with cinchona modified Pt catalyst
    • Studer, M., Burkhardt, S., Blaser, H. U. (1999). Enantioselective hydrogenation of alpha-keto acetals with cinchona modified Pt catalyst. Chem. Commun., 1727-1728.
    • (1999) Chem. Commun., , pp. 1727-1728
    • Studer, M.1    Burkhardt, S.2    Blaser, H.U.3
  • 69
    • 23444454990 scopus 로고    scopus 로고
    • Chemo and enantioselective hydrogenation of fluorinated ketones on platinum modified with (R)-1-(1-naphthyl)ethylamine derivatives
    • Diezi, S., Hess, M., Orglmeister, E., Mallat, T., Baiker, A. (2005). Chemo and enantioselective hydrogenation of fluorinated ketones on platinum modified with (R)-1-(1-naphthyl)ethylamine derivatives. J. Mol. Catal. A Chem., 239, 49-56.
    • (2005) J. Mol. Catal. A Chem., , vol.239 , pp. 49-56
    • Diezi, S.1    Hess, M.2    Orglmeister, E.3    Mallat, T.4    Baiker, A.5
  • 71
    • 0035842865 scopus 로고    scopus 로고
    • Platinum-catalyzed enantioselective hydrogenation of aryl-substituted trifluoroacetophenones
    • von Arx, M., Mallat, T., Baiker, A. (2001). Platinum-catalyzed enantioselective hydrogenation of aryl-substituted trifluoroacetophenones. Tetrahedron Asymmetry, 12, 3089-3094.
    • (2001) Tetrahedron Asymmetry, , vol.12 , pp. 3089-3094
    • von Arx, M.1    Mallat, T.2    Baiker, A.3
  • 73
    • 0002879377 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of trifluoroacetophenone over cinchonidine-modified platinum
    • Mallat, T., Bodmer, M., Balker, A. (1997). Enantioselective hydrogenation of trifluoroacetophenone over cinchonidine-modified platinum. Catal. Lett., 44, 95-99.
    • (1997) Catal. Lett , vol.44 , pp. 95-99
    • Mallat, T.1    Bodmer, M.2    Balker, A.3
  • 74
    • 0346339551 scopus 로고    scopus 로고
    • Chemo-and enantioselective hydrogenation of the activated keto group of fluorinated beta-diketones
    • Hess, R., Diezi, S., Mallat, T., Baiker, A. (2004). Chemo-and enantioselective hydrogenation of the activated keto group of fluorinated beta-diketones. Tetrahedron Asymmetry, 15, 251-257.
    • (2004) Tetrahedron Asymmetry , vol.15 , pp. 251-257
    • Hess, R.1    Diezi, S.2    Mallat, T.3    Baiker, A.4
  • 75
    • 0036494555 scopus 로고    scopus 로고
    • Highly efficient platinum-catalyzed enantio selective hydrogenation of trifluoroacetoacetates in acidic solvents
    • von Arx, M., Mallat, T., Baiker, A. (2002). Highly efficient platinum-catalyzed enantio selective hydrogenation of trifluoroacetoacetates in acidic solvents. Catal. Lett., 78, 267-271.
    • (2002) Catal. Lett., , vol.78 , pp. 267-271
    • von Arx, M.1    Mallat, T.2    Baiker, A.3
  • 76
    • 33645934203 scopus 로고    scopus 로고
    • Dynamic kinetic resolution over Cinchona-modified platinum catalyst: hydrogenation of racemic ethyl 2-fluoroacetoacetate
    • Szöri, K., Szöllösi, G., Bartók, M. (2006). Dynamic kinetic resolution over Cinchona-modified platinum catalyst: hydrogenation of racemic ethyl 2-fluoroacetoacetate. Adv. Synth. Catal., 348, 515-522.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 515-522
    • Szöri, K.1    Szöllösi, G.2    Bartók, M.3
  • 77
    • 33646194964 scopus 로고    scopus 로고
    • Steric and electronic effects in enantioselective hydrogenation of ketones on platinum modified by cinchonidine: directing effect of the trifluoromethyl group
    • Vargas, A., Hoxha, F., Bonalumi, N., Mallat, T., Baiker, A. (2006). Steric and electronic effects in enantioselective hydrogenation of ketones on platinum modified by cinchonidine: directing effect of the trifluoromethyl group. J. Catal., 240, 203-212.
    • (2006) J. Catal., , vol.240 , pp. 203-212
    • Vargas, A.1    Hoxha, F.2    Bonalumi, N.3    Mallat, T.4    Baiker, A.5
  • 78
    • 17144446111 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of trifluoromethylcyclohexyl ketone on cinchona alkaloid modified Pt - alumina catalyst
    • Felföldi, K., Varga, T., Forg ó, P., Bartók, M. (2004). Enantioselective hydrogenation of trifluoromethylcyclohexyl ketone on cinchona alkaloid modified Pt - alumina catalyst. Catal. Lett., 97, 65-70.
    • (2004) Catal. Lett , vol.97 , pp. 65-70
    • Felföldi, K.1    Varga, T.2    Forgó, P.3    Bartók, M.4
  • 79
    • 0000582327 scopus 로고
    • Modified Raney-Nickel (MRNi) catalyst - heterogeneous enantio-differentiating (asymmetric) catalyst
    • Izumi, Y. (1983). Modified Raney-Nickel (MRNi) catalyst - heterogeneous enantio-differentiating (asymmetric) catalyst. Adv. Catal., 32, 215-271.
    • (1983) Adv. Catal , vol.32 , pp. 215-271
    • Izumi, Y.1
  • 80
    • 0001915257 scopus 로고
    • Asymmetric sites on heterogeneous catalysts. In: R. L. Augustine (Ed.), Catalysis of Organic Reactions
    • Sachtler, W. M. (1985). Asymmetric sites on heterogeneous catalysts. In: R. L. Augustine (Ed.), Catalysis of Organic Reactions. M. Dekker, New York, p. 189.
    • (1985) M. Dekker, New York , pp. 189
    • Sachtler, W.M.1
  • 81
    • 0002273951 scopus 로고
    • Asymmetrically modified nickel catalysts
    • (Ed.), Tailored Metal Catalysts. D. Reidel, Dordrecht, South Africa
    • Tai, A., Harada, T. (1986). Asymmetrically modified nickel catalysts. In: Y. Iwasawa (Ed.), Tailored Metal Catalysts. D. Reidel, Dordrecht, South Africa, p. 265.
    • (1986) In: Y. Iwasawa , pp. 265
    • Tai, A.1    Harada, T.2
  • 82
    • 0003492617 scopus 로고    scopus 로고
    • Modified Ni catalysts for enantiodifferentiating hydrogenation
    • (Eds.), C hiral Catalyst Immobilization and Recycling. Wiley-VCH, Weinheim, Germany
    • Tai, A., Sugimura, T. (2000). Modified Ni catalysts for enantiodifferentiating hydrogenation. In: D. E. De Vos, I. F. J. Vankelecom, P. A. Jacobs (Eds.), C hiral Catalyst Immobilization and Recycling. Wiley-VCH, Weinheim, Germany, p. 173.
    • (2000) In: D. E. De Vos, I. F. J. Vankelecom, P. A. Jacobs , pp. 173
    • Tai, A.1    Sugimura, T.2
  • 83
    • 0033114710 scopus 로고    scopus 로고
    • Recent progress in tartaric acid-modified Raney nickel system for enantio-differentiating hydrogenation
    • Sugimura, T. (1999). Recent progress in tartaric acid-modified Raney nickel system for enantio-differentiating hydrogenation. Catal. Surv. Jpn., 3, 37-42.
    • (1999) Catal. Surv. Jpn , vol.3 , pp. 37-42
    • Sugimura, T.1
  • 84
    • 33748510573 scopus 로고    scopus 로고
    • Asymmetrically modified nickel catalyst for the enantio-differentiating hydrogenation of prochiral ketones
    • Osawa, T., Harada, T., Takayasu, O. (2006). Asymmetrically modified nickel catalyst for the enantio-differentiating hydrogenation of prochiral ketones. Curr. Org. Chem., 10, 1513-1531.
    • (2006) Curr. Org. Chem., , vol.10 , pp. 1513-1531
    • Osawa, T.1    Harada, T.2    Takayasu, O.3
  • 85
    • 0000941209 scopus 로고    scopus 로고
    • Enantio-differentiating hydrogenation of prochiral ketones over modified nickel
    • Osawa, T., Harada, T., Tai, A. (1997). Enantio-differentiating hydrogenation of prochiral ketones over modified nickel. Catal. Today., 37, 465-480.
    • (1997) Catal. Today., , vol.37 , pp. 465-480
    • Osawa, T.1    Harada, T.2    Tai, A.3
  • 86
    • 0342682440 scopus 로고
    • On some general regularities in the action of enantioselective hydrogenation catalysts
    • Klabunovskii, E. I. (1991). On some general regularities in the action of enantioselective hydrogenation catalysts. J. Organomet. Chem., 417, 181-191.
    • (1991) J. Organomet. Chem., , vol.417 , pp. 181-191
    • Klabunovskii, E.I.1
  • 87
    • 16544390286 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of beta-hydroxyacids and their esters
    • Klabunovskii, E. I. (1996). Catalytic asymmetric synthesis of beta-hydroxyacids and their esters. Russ. Chem. Rev., 65, 329-344.
    • (1996) Russ. Chem. Rev., , vol.65 , pp. 329-344
    • Klabunovskii, E.I.1
  • 88
    • 0031558998 scopus 로고    scopus 로고
    • Interaction of optically active tartaric acid with a nickel - silica catalyst: role of both the modification and reaction media in determining enantioselectivity
    • Keane, M. A. (1997). Interaction of optically active tartaric acid with a nickel - silica catalyst: role of both the modification and reaction media in determining enantioselectivity. Langmuir, 13, 41-50.
    • (1997) Langmuir, , vol.13 , pp. 41-50
    • Keane, M.A.1
  • 89
    • 84885988029 scopus 로고    scopus 로고
    • Asymmetrically modified nickel catalysts
    • (Ed.), Catalysis of Organic Reactions. Dekker, New York
    • Tai, A. (2003). Asymmetrically modified nickel catalysts. In: D. G. Morrell (Ed.), Catalysis of Organic Reactions. Dekker, New York, p. 191.
    • (2003) In: D. G. Morrell , pp. 191
    • Tai, A.1
  • 90
    • 30444437616 scopus 로고    scopus 로고
    • In situ chiral modification of nickel catalysts for enantioselective hydrogenation of methyl acetoacetate
    • Bartek, L., Kluson, P., Cerveny, L. (2005). In situ chiral modification of nickel catalysts for enantioselective hydrogenation of methyl acetoacetate. Collect. Czech. Chem. Commun., 70, 1642-1652.
    • (2005) Collect. Czech. Chem. Commun., , vol.70 , pp. 1642-1652
    • Bartek, L.1    Kluson, P.2    Cerveny, L.3
  • 91
    • 33845453627 scopus 로고    scopus 로고
    • Studies of the effects of the modification conditions on the hydrogenation rate for the enantio - differentiating hydrogenation of methyl acetoacetate over a tartaric acid-NaBr - modified nickel catalyst
    • Osawa, T., Hagino, Y., Harada, T., Takayasu, O. (2006). Studies of the effects of the modification conditions on the hydrogenation rate for the enantio - differentiating hydrogenation of methyl acetoacetate over a tartaric acid-NaBr - modified nickel catalyst. Catal. Lett., 112, 57-61.
    • (2006) Catal. Lett., , vol.112 , pp. 57-61
    • Osawa, T.1    Hagino, Y.2    Harada, T.3    Takayasu, O.4
  • 92
    • 33845502029 scopus 로고    scopus 로고
    • Enantio - differentiating hydrogenation of methyl acetoacetate over modified Raney nickel catalysts prepared by two-step modifications
    • Osawa, T., Yoshino, K., Takimoto, K., Takayasu, O., Harada, T. (2006). Enantio - differentiating hydrogenation of methyl acetoacetate over modified Raney nickel catalysts prepared by two-step modifications. Catal. Lett., 112, 167-171.
    • (2006) Catal. Lett., , vol.112 , pp. 167-171
    • Osawa, T.1    Yoshino, K.2    Takimoto, K.3    Takayasu, O.4    Harada, T.5
  • 93
    • 33645415717 scopus 로고    scopus 로고
    • Enantiomer - differentiating hydrogenation of methyl 3-cyclopropyl-2-methyl-3-oxopropanoate over tartaric acid-modified nickel - performance of heterogeneous catalyst in dynamic kinetic resolution
    • Sugimura, T., Watanabe, J., Nakagawa, S., Okuyama, T. (2006). Enantiomer - differentiating hydrogenation of methyl 3-cyclopropyl-2-methyl-3-oxopropanoate over tartaric acid-modified nickel - performance of heterogeneous catalyst in dynamic kinetic resolution. J. Mol. Catal. A Chem., 248, 233-236.
    • (2006) J. Mol. Catal. A Chem., , vol.248 , pp. 233-236
    • Sugimura, T.1    Watanabe, J.2    Nakagawa, S.3    Okuyama, T.4
  • 95
    • 0000729772 scopus 로고    scopus 로고
    • Progress of enantio-differentiating hydrogenation of prochiral ketones over asymmetrically modified nickel catalysts and a newly proposed enantio-differentiation model
    • Osawa, T., Harada, T., Takayasu, O. (2000). Progress of enantio-differentiating hydrogenation of prochiral ketones over asymmetrically modified nickel catalysts and a newly proposed enantio-differentiation model. Top. Catal., 13, 155-168.
    • (2000) Top. Catal., , vol.13 , pp. 155-168
    • Osawa, T.1    Harada, T.2    Takayasu, O.3
  • 96
    • 0002763124 scopus 로고
    • Enantio-differentiating hydrogenation of 2-alkanones over asymmetrically modified nickel-catalyst and its application to the preparation of optically pure 2-alkanols
    • Osawa, T., Harada, T., Tai, A. (1990). Enantio-differentiating hydrogenation of 2-alkanones over asymmetrically modified nickel-catalyst and its application to the preparation of optically pure 2-alkanols. J. Catal., 121, 7-17.
    • (1990) J. Catal., , vol.121 , pp. 7-17
    • Osawa, T.1    Harada, T.2    Tai, A.3
  • 97
    • 0028516960 scopus 로고
    • Enantioface - differentiating hydrogenation of the C = O double-bond using a modified Raney - Nickel - role of the carboxylic-acid added to the reaction system
    • Harada, T., Kawamura, T., Haikawa, S., Osawa, T. (1994). Enantioface - differentiating hydrogenation of the C = O double-bond using a modified Raney - Nickel - role of the carboxylic-acid added to the reaction system. J. Mol. Catal., 93, 211-219.
    • (1994) J. Mol. Catal., , vol.93 , pp. 211-219
    • Harada, T.1    Kawamura, T.2    Haikawa, S.3    Osawa, T.4
  • 98
    • 0028763726 scopus 로고
    • Mode of enantioface-differentiation in the hydrogenation of 2-alkanone over an asymmetrically modified nickel-catalyst
    • Osawa, T., Harada, T., Tai, A. (1994). Mode of enantioface-differentiation in the hydrogenation of 2-alkanone over an asymmetrically modified nickel-catalyst. J. Mol. Catal., 87, 333-342.
    • (1994) J. Mol. Catal., , vol.87 , pp. 333-342
    • Osawa, T.1    Harada, T.2    Tai, A.3
  • 99
    • 33845495337 scopus 로고    scopus 로고
    • Studies of the effect of pivalic acid on the hydrogenation rate and the enantio-differentiating ability for the hydrogenation of 2-octanone over a tartaric acid-NaBr-modified nickel catalyst
    • Osawa, T., Nakagawa, Y., Harada, T., Takayasu, O. (2006). Studies of the effect of pivalic acid on the hydrogenation rate and the enantio-differentiating ability for the hydrogenation of 2-octanone over a tartaric acid-NaBr-modified nickel catalyst . Catal. Lett., 112, 163-166.
    • (2006) Catal. Lett., , vol.112 , pp. 163-166
    • Osawa, T.1    Nakagawa, Y.2    Harada, T.3    Takayasu, O.4
  • 100
    • 33644857130 scopus 로고    scopus 로고
    • MCM-41-supported platinum carbonyl cluster-derived catalysts for asymmetric and nonasymmetric hydrogenation reactions
    • Basu, S., Mapa, M., Gopinath, C. S., Doble, M., Bhaduri, S., Lahiri, G. K. (2006). MCM-41-supported platinum carbonyl cluster-derived catalysts for asymmetric and nonasymmetric hydrogenation reactions. J. Catal., 239, 154-161.
    • (2006) J. Catal., , vol.239 , pp. 154-161
    • Basu, S.1    Mapa, M.2    Gopinath, C.S.3    Doble, M.4    Bhaduri, S.5    Lahiri, G.K.6
  • 101
    • 3442901923 scopus 로고    scopus 로고
    • New approach toward the synthesis of asymmetric heterogeneous catalysts for hydrogenation reactions
    • Vetere, V., Faraoni, M. B., Santori, G. F., Podesta, J., Casella, M. L., Ferretti, O. A. (2004). New approach toward the synthesis of asymmetric heterogeneous catalysts for hydrogenation reactions. J. Catal., 226, 457-461.
    • (2004) J. Catal., , vol.226 , pp. 457-461
    • Vetere, V.1    Faraoni, M.B.2    Santori, G.F.3    Podesta, J.4    Casella, M.L.5    Ferretti, O.A.6
  • 102
    • 0026188008 scopus 로고
    • Enantioselective hydrogenation of acetophenone in the presence of s-proline
    • Tungler, A., Tarnai, T., Mathe, T., Petro, J. (1991). Enantioselective hydrogenation of acetophenone in the presence of s-proline. J. Mol. Catal., 67, 277-282.
    • (1991) J. Mol. Catal., , vol.67 , pp. 277-282
    • Tungler, A.1    Tarnai, T.2    Mathe, T.3    Petro, J.4
  • 103
    • 26844518144 scopus 로고    scopus 로고
    • Study of the racemic and enantioselective hydrogenation of acetophenone and 3,4-dimethoxyacetophenone using platinum-based organotin catalysts
    • Vetere, V., Faraoni, M. B. E., Santori, G. F., Podesta, J. U., Casella, M. L., Ferretti, O. A. (2005). Study of the racemic and enantioselective hydrogenation of acetophenone and 3,4-dimethoxyacetophenone using platinum-based organotin catalysts . Catal. Today, 107-108, 266-272.
    • (2005) Catal. Today, 107-108, , pp. 266-272
    • Vetere, V.1    Faraoni, M.B.E.2    Santori, G.F.3    Podesta, J.U.4    Casella, M.L.5    Ferretti, O.A.6
  • 104
    • 0842283261 scopus 로고    scopus 로고
    • Inversion of enantioselectivity in the platinum-catalyzed hydrogenation of substituted acetophenones
    • Hess, R., Vargas, A., Mallat, T., Burgi, T., Baiker, A. (2004). Inversion of enantioselectivity in the platinum-catalyzed hydrogenation of substituted acetophenones . J. Catal., 222, 117-128.
    • (2004) J. Catal., , vol.222 , pp. 117-128
    • Hess, R.1    Vargas, A.2    Mallat, T.3    Burgi, T.4    Baiker, A.5
  • 105
    • 0141455171 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of aromatic ketones: structural effects
    • Hess, R., Mallat, T., Baiker, A. (2003). Enantioselective hydrogenation of aromatic ketones: structural effects. J. Catal., 218, 453-456.
    • (2003) J. Catal., , vol.218 , pp. 453-456
    • Hess, R.1    Mallat, T.2    Baiker, A.3
  • 106
    • 70349869490 scopus 로고    scopus 로고
    • Asymmetric hydrogenations of acetophenone and its derivatives over Ir/HAP modified by (1S,2S)-DPEN
    • Zhang, D. L., Yang, C. F., Feng, J., Fu, H. Y., Chen, H., Li, R. X., Li, X. J. (2009). Asymmetric hydrogenations of acetophenone and its derivatives over Ir/HAP modified by (1S,2S)-DPEN. Acta Phys-Chim. Sin., 25, 2039-2044.
    • (2009) Acta Phys-Chim. Sin., , vol.25 , pp. 2039-2044
    • Zhang, D.L.1    Yang, C.F.2    Feng, J.3    Fu, H.Y.4    Chen, H.5    Li, R.X.6    Li, X.J.7
  • 107
    • 41349085563 scopus 로고    scopus 로고
    • Enantio selective hydrogenation of 1-phenyl-1,2-propanedione, ethyl pyruvate and acetophenone on Ir/SiO 2 catalysts effect of iridium loading
    • Marzialetti, T., Oportus, M., Ruiz, D., Fierro, J. L. G., Reyes, P. (2008). Enantio selective hydrogenation of 1-phenyl-1,2-propanedione, ethyl pyruvate and acetophenone on Ir/SiO 2 catalysts effect of iridium loading. Catal. Today, 133, 711-719.
    • (2008) Catal. Today, , vol.133 , pp. 711-719
    • Marzialetti, T.1    Oportus, M.2    Ruiz, D.3    Fierro, J.L.G.4    Reyes, P.5
  • 108
    • 59549085360 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of acetophenone catalyzed by cinchonidine stabilized Ir/SiO 2
    • Yang, C. F., Jiang, H. Y., Feng, J., Fu, H. Y., Li, R. X., Chen, H., Li, X. J. (2009). Asymmetric hydrogenation of acetophenone catalyzed by cinchonidine stabilized Ir/SiO 2. J. Mol. Catal. A Chem., 300, 98-102.
    • (2009) J. Mol. Catal. A Chem., , vol.300 , pp. 98-102
    • Yang, C.F.1    Jiang, H.Y.2    Feng, J.3    Fu, H.Y.4    Li, R.X.5    Chen, H.6    Li, X.J.7
  • 109
    • 35748974154 scopus 로고    scopus 로고
    • R,R)-DPEN-modified Ru/gamma-Al 2 O 3 - an efficient heterogeneous catalyst for enantioselective hydrogenation of acetophenone
    • Cheng, H. Y., Hao, J. M., Wang, H. J., Xi, C. Y., Meng, X. C., Cai, S. X., Zhao, F. Y. (2007). R,R)-DPEN-modified Ru/gamma-Al 2 O 3 - an efficient heterogeneous catalyst for enantioselective hydrogenation of acetophenone. J. Mol. Catal. A Chem., 278, 6-11.
    • (2007) J. Mol. Catal. A Chem., , vol.278 , pp. 6-11
    • Cheng, H.Y.1    Hao, J.M.2    Wang, H.J.3    Xi, C.Y.4    Meng, X.C.5    Cai, S.X.6    Zhao, F.Y.7
  • 110
    • 47249121648 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of aromatic ketones catalyzed by (1S,2S)-DPEN - modified Ru- PPh 3 /gamma- Al 2 O 3 catalyst
    • Tang, B., Xiong, W., Liu, E. R., Jia, Y., Wang, J. B., Chen, H., Li, X. J. (2008). Asymmetric hydrogenation of aromatic ketones catalyzed by (1S,2S)-DPEN - modified Ru- PPh 3 /gamma- Al 2 O 3 catalyst. Tetrahedron Asymmetry, 19, 1397-1401.
    • (2008) Tetrahedron Asymmetry, , vol.19 , pp. 1397-1401
    • Tang, B.1    Xiong, W.2    Liu, E.R.3    Jia, Y.4    Wang, J.B.5    Chen, H.6    Li, X.J.7
  • 111
    • 56449101209 scopus 로고    scopus 로고
    • Heterogeneous enantioselective hydrogenation of aromatic ketones catalyzed by Cinchona-and phosphine-modified iridium catalysts
    • Jiang, H. Y., Yang, C. F., Li, C., Fu, H. Y., Chen, H., Li, R. X., Li, X. J. (2008). Heterogeneous enantioselective hydrogenation of aromatic ketones catalyzed by Cinchona-and phosphine-modified iridium catalysts. Angew. Chem. Int. Ed., 47, 9240-9244.
    • (2008) Angew. Chem. Int. Ed., , vol.47 , pp. 9240-9244
    • Jiang, H.Y.1    Yang, C.F.2    Li, C.3    Fu, H.Y.4    Chen, H.5    Li, R.X.6    Li, X.J.7
  • 112
    • 0003112794 scopus 로고    scopus 로고
    • Enantioselective hydrogenation with solid catalysts. In: R. A. Sheldon, H. van Bekkum (Eds.), Fine Chemicals through Heterogeneous Catalysis
    • Mallat, T., Baiker, A., (2001). Enantioselective hydrogenation with solid catalysts. In: R. A. Sheldon, H. van Bekkum (Eds.), Fine Chemicals through Heterogeneous Catalysis. Wiley-VCH, Weinheim, Germany, p. 449.
    • (2001) Wiley-VCH, Weinheim, Germany , pp. 449
    • Mallat, T.1    Baiker, A.2
  • 113
    • 0035839711 scopus 로고    scopus 로고
    • Catalysis with supported palladium metal, selectivity in the hydrogenation of C = C, C = O and C = N bonds, from chemo-to enantioselectivity
    • Tungler, A., Fogassy, G. (2001). Catalysis with supported palladium metal, selectivity in the hydrogenation of C = C, C = O and C = N bonds, from chemo-to enantioselectivity . J. Mol. Catal. A Chem., 173, 231-247.
    • (2001) J. Mol. Catal. A Chem , vol.173 , pp. 231-247
    • Tungler, A.1    Fogassy, G.2
  • 114
    • 2542479136 scopus 로고    scopus 로고
    • New substrates and modifiers in the enantio selective heterogeneous catalytic hydrogenation of the C = C double bond
    • Sipos, E., Tungler, A., Fogassy, G. (2004). New substrates and modifiers in the enantio selective heterogeneous catalytic hydrogenation of the C = C double bond. J. Mol. Catal. A Chem., 216, 171-180.
    • (2004) J. Mol. Catal. A Chem , vol.216 , pp. 171-180
    • Sipos, E.1    Tungler, A.2    Fogassy, G.3
  • 115
    • 0342910617 scopus 로고
    • Stereospecific hydrogenations using palladium-on-silica gel catalysts
    • Padgett, R. E., Beamer, R. L. (1964). Stereospecific hydrogenations using palladium-on-silica gel catalysts. J. Pharm. Sci., 5 3, 689-690.
    • (1964) J. Pharm. Sci., 5 , vol.3 , pp. 689-690
    • Padgett, R.E.1    Beamer, R.L.2
  • 116
    • 0001119668 scopus 로고
    • Asymmetric hydrogenation of prochiral cinnamic-acids in the presence of palladium on activated carbon and of chiral bases
    • Perez, J. R. G., Malthete, J., Jacques, J. (1985). Asymmetric hydrogenation of prochiral cinnamic-acids in the presence of palladium on activated carbon and of chiral bases. C.R. Acad. Sci. II, 300, 169-172.
    • (1985) C.R. Acad. Sci. II, , vol.300 , pp. 169-172
    • Perez, J.R.G.1    Malthete, J.2    Jacques, J.3
  • 117
    • 0000523804 scopus 로고
    • Enantioselective hydrogenation of (E) - alpha-phenylcinnamic acid over cinchonidine-modified palladium catalysts
    • Nitta, Y., Ueda, Y., Imanaka, T. (1994). Enantioselective hydrogenation of (E) - alpha-phenylcinnamic acid over cinchonidine-modified palladium catalysts. Chem. Lett., 23, 1095-1098.
    • (1994) Chem. Lett., , vol.23 , pp. 1095-1098
    • Nitta, Y.1    Ueda, Y.2    Imanaka, T.3
  • 119
    • 0034253388 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of (E)-alpha-phenylcinnamic acid with cinchonidine-modified Pd/TiO 2: influence of solvents and additives
    • Nitta, Y. (2000). Enantioselective hydrogenation of (E)-alpha-phenylcinnamic acid with cinchonidine-modified Pd/TiO 2: influence of solvents and additives. Top. Catal., 13, 179-185.
    • (2000) Top. Catal., , vol.13 , pp. 179-185
    • Nitta, Y.1
  • 120
    • 0035788699 scopus 로고    scopus 로고
    • Effect of palladium dispersion on the enantioselective hydrogenation of alpha,beta-unsaturated acids with modified Pd/TiO 2 catalysts
    • Nitta, Y., Kubota, T., Okamoto, Y. (2001). Effect of palladium dispersion on the enantioselective hydrogenation of alpha,beta-unsaturated acids with modified Pd/TiO 2 catalysts. Bull. Chem. Soc. Jpn., 74, 2161-2165.
    • (2001) Bull. Chem. Soc. Jpn , vol.74 , pp. 2161-2165
    • Nitta, Y.1    Kubota, T.2    Okamoto, Y.3
  • 121
    • 1242340330 scopus 로고    scopus 로고
    • Solvent effect on the structure sensitivity in enantioselective hydrogenation of alpha, beta-unsaturated acids with modified palladium catalysts
    • Nitta, Y., Kubota, T., Okamoto, Y. (2004). Solvent effect on the structure sensitivity in enantioselective hydrogenation of alpha, beta-unsaturated acids with modified palladium catalysts. J. Mol. Catal. A Chem., 212, 155-159.
    • (2004) J. Mol. Catal. A Chem., , vol.212 , pp. 155-159
    • Nitta, Y.1    Kubota, T.2    Okamoto, Y.3
  • 122
    • 27644469490 scopus 로고    scopus 로고
    • Activation-temperature dependence in enantioselective hydrogenation of unsaturated carboxylic acids over cinchonidine-modified Pd/C catalysts
    • Nitta, Y., Watanabe, J., Okuyama, T., Sugimura, T. (2005). Activation-temperature dependence in enantioselective hydrogenation of unsaturated carboxylic acids over cinchonidine-modified Pd/C catalysts. J. Catal., 236, 164-167.
    • (2005) J. Catal., , vol.236 , pp. 164-167
    • Nitta, Y.1    Watanabe, J.2    Okuyama, T.3    Sugimura, T.4
  • 123
    • 17844408672 scopus 로고    scopus 로고
    • The effect of the substrate structure on the stereoselectivity in an asymmetric hydrogenation of unsaturated carboxylic acids over cinchonidine-modified palladium catalyst
    • Sugimura, T., Watanabe, J., Okuyama, T., Nitta, Y. (2005). The effect of the substrate structure on the stereoselectivity in an asymmetric hydrogenation of unsaturated carboxylic acids over cinchonidine-modified palladium catalyst. Tetrahedron Asymmetry, 16, 1573-1575.
    • (2005) Tetrahedron Asymmetry, , vol.16 , pp. 1573-1575
    • Sugimura, T.1    Watanabe, J.2    Okuyama, T.3    Nitta, Y.4
  • 127
    • 0004981515 scopus 로고    scopus 로고
    • Chiral modifiers for supported metals. In: M. E. Ford (Ed.), Catalysis of Organic Reactions
    • Testa, A. C., Augustine, R. L. (2000). Chiral modifiers for supported metals. In: M. E. Ford (Ed.), Catalysis of Organic Reactions. M. Dekker, New York, p. 465.
    • (2000) M. Dekker, New York , pp. 465
    • Testa, A.C.1    Augustine, R.L.2
  • 128
    • 0004981515 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of unsaturated carboxylic acids over palladium modified by a substituted binaphthylene. In: M. E. Ford (Ed.), Catalysis of Organic Reactions
    • Jackson, S. D., Watson, S. R., Webb, G., Wells, P. B., Young, N. C. (2000). Enantioselective hydrogenation of unsaturated carboxylic acids over palladium modified by a substituted binaphthylene. In: M. E. Ford (Ed.), Catalysis of Organic Reactions. M. Dekker, New York, p. 477.
    • (2000) M. Dekker, New York , pp. 477
    • Jackson, S.D.1    Watson, S.R.2    Webb, G.3    Wells, P.B.4    Young, N.C.5
  • 129
    • 0037102072 scopus 로고    scopus 로고
    • In situ ATR-IR study of the adsorption of cinchonidine on Pd/Al2O3: differences and similarities with adsorption on Pt/ Al2O3
    • Ferri, D., Bürgi, T., Baiker, A. (2002). In situ ATR-IR study of the adsorption of cinchonidine on Pd/Al2O3: differences and similarities with adsorption on Pt/ Al2O3. J. Catal., 210, 160-170.
    • (2002) J. Catal., , vol.210 , pp. 160-170
    • Ferri, D.1    Bürgi, T.2    Baiker, A.3
  • 130
    • 0033474785 scopus 로고    scopus 로고
    • Importance of product desorption in enantioselective hydrogenation of (E)-alpha-phenylcinnamic acid with a cinchonidine-modified Pd/TiO 2 catalyst: effect of additives
    • Nitta, Y. (1999). Importance of product desorption in enantioselective hydrogenation of (E)-alpha-phenylcinnamic acid with a cinchonidine-modified Pd/TiO 2 catalyst: effect of additives. Chem. Lett., 28, 635-636.
    • (1999) Chem. Lett., , vol.28 , pp. 635-636
    • Nitta, Y.1
  • 132
    • 0001025531 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of (E)-alpha - phenylcinnamic acid on Pd/TiO 2 catalyst modified by cinchona alkaloids: effect of modifier structure
    • Nitta, Y., Shibata, A. (1998). Enantioselective hydrogenation of (E)-alpha - phenylcinnamic acid on Pd/TiO 2 catalyst modified by cinchona alkaloids: effect of modifier structure. Chem. Lett., 27, 161-162.
    • (1998) Chem. Lett., , vol.27 , pp. 161-162
    • Nitta, Y.1    Shibata, A.2
  • 133
    • 33845432694 scopus 로고    scopus 로고
    • Highly enantioselective hydrogenation of alpha-Alkyl-beta-arylpropenoic acids over cinchonidine-modified palladium catalyst
    • Sugimura, T., Watanabe, J., Uchida, T., Nitta, Y., Okuyama, T. (2006). Highly enantioselective hydrogenation of alpha-Alkyl-beta-arylpropenoic acids over cinchonidine-modified palladium catalyst. Catal. Lett., 112, 27-30.
    • (2006) Catal. Lett., , vol.112 , pp. 27-30
    • Sugimura, T.1    Watanabe, J.2    Uchida, T.3    Nitta, Y.4    Okuyama, T.5
  • 134
    • 0033370161 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of indene carboxylic acids: stereochemistry of hydrogen addition
    • Borszeky, K., Mallat, T., Baiker, A. (1999). Asymmetric hydrogenation of indene carboxylic acids: stereochemistry of hydrogen addition. Tetrahedron Asymmetry, 10, 4781-4789.
    • (1999) Tetrahedron Asymmetry, , vol.10 , pp. 4781-4789
    • Borszeky, K.1    Mallat, T.2    Baiker, A.3
  • 136
    • 15244352434 scopus 로고    scopus 로고
    • The solvent effect in the enantioselective hydrogenation of (E)-2-methyl-2-butenoic acid with cinchonidine doped Pd/Al 2 O 3
    • Bisignani, R., Franceschini, S., Piccolo, O., Vaccari, A. (2005). The solvent effect in the enantioselective hydrogenation of (E)-2-methyl-2-butenoic acid with cinchonidine doped Pd/Al 2 O 3. J. Mol. Catal. A Chem., 232, 161-164.
    • (2005) J. Mol. Catal. A Chem., , vol.232 , pp. 161-164
    • Bisignani, R.1    Franceschini, S.2    Piccolo, O.3    Vaccari, A.4
  • 137
    • 32844465493 scopus 로고    scopus 로고
    • Cinchonidine doped Pd catalysts in the enantioselective hydrogenation of (E) - 2-methyl-2-butenoic acid
    • Casagrande, A., Franceschini, S., Lenarda, M., Piccolo, O., Vaccari, A. (2006). Cinchonidine doped Pd catalysts in the enantioselective hydrogenation of (E) - 2-methyl-2-butenoic acid. J. Mol. Catal. A Chem., 246, 263-267.
    • (2006) J. Mol. Catal. A Chem., , vol.246 , pp. 263-267
    • Casagrande, A.1    Franceschini, S.2    Lenarda, M.3    Piccolo, O.4    Vaccari, A.5
  • 138
  • 139
    • 0037452940 scopus 로고    scopus 로고
    • Heterogeneous asymmetric hydrogenation and deuteration of 2-methyl-2-pentenoic acid over Pd supported catalysts: proton/deuterium exchange
    • Solladie-Cavallo, A., Hoernel, F., Schmitt, M., Garin, F. (2003). Heterogeneous asymmetric hydrogenation and deuteration of 2-methyl-2-pentenoic acid over Pd supported catalysts: proton/deuterium exchange. J. Mol. Catal. A Chem., 195, 181-188.
    • (2003) J. Mol. Catal. A Chem., , vol.195 , pp. 181-188
    • Solladie-Cavallo, A.1    Hoernel, F.2    Schmitt, M.3    Garin, F.4
  • 140
    • 17444394525 scopus 로고    scopus 로고
    • A novel asymmetric heterogeneous catalytic reaction: hydrogenation of ethyl 2-acetoxyacrylate on cinchonidine modified Pd and Pt catalyst
    • Szöri, K., Szöllösi, G., Felföldi, K., Bartók, M. (2005). A novel asymmetric heterogeneous catalytic reaction: hydrogenation of ethyl 2-acetoxyacrylate on cinchonidine modified Pd and Pt catalyst. React. Kinet. Catal. Lett., 84, 151-156.
    • (2005) React. Kinet. Catal. Lett., , vol.84 , pp. 151-156
    • Szöri, K.1    Szöllösi, G.2    Felföldi, K.3    Bartók, M.4
  • 141
    • 0345561665 scopus 로고    scopus 로고
    • Enantioselective synthesis of ethyl nipecotinate using cinchona modified heterogeneous catalysts
    • Blaser, H. U., Hönig, H., Studer, M., Wedemeyer-Exl, C. (1999). Enantioselective synthesis of ethyl nipecotinate using cinchona modified heterogeneous catalysts. J. Mol. Catal. A Chem., 139, 253-257.
    • (1999) J. Mol. Catal. A Chem., , vol.139 , pp. 253-257
    • Blaser, H.U.1    Hönig, H.2    Studer, M.3    Wedemeyer-Exl, C.4
  • 143
    • 23944512874 scopus 로고    scopus 로고
    • Unexpected inversion in enantioselectivity in the hydrogenation N-acetyl dehydrophenylalanine methyl ester using cinchona-modified Pd/Al 2 O 3 catalyst
    • Colston, N. J., Wells, R. P. K., Wells, P. B., Hutchings, G. J. (2005). Unexpected inversion in enantioselectivity in the hydrogenation N-acetyl dehydrophenylalanine methyl ester using cinchona-modified Pd/Al 2 O 3 catalyst. Catal. Lett., 103, 117-120.
    • (2005) Catal. Lett., , vol.103 , pp. 117-120
    • Colston, N.J.1    Wells, R.P.K.2    Wells, P.B.3    Hutchings, G.J.4
  • 144
    • 33646245421 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of N-acetyl dehydrophenylalanine methyl ester using cinchonine - modified Pd/TiO 2 catalysts
    • Coulston, N. J., Wells, R. P. K., Wells, P. B., Hutchings, G. J. (2006). Enantioselective hydrogenation of N-acetyl dehydrophenylalanine methyl ester using cinchonine - modified Pd/TiO 2 catalysts. Catal. Today, 114, 353-356.
    • (2006) Catal. Today, , vol.114 , pp. 353-356
    • Coulston, N.J.1    Wells, R.P.K.2    Wells, P.B.3    Hutchings, G.J.4
  • 147
    • 0027418236 scopus 로고
    • Stereochemistry of the enantioselective reductive alkylation of proline with ketones
    • Tóth, G., Kovàcs, A., Tarnai, T., Tungler, A. (1993). Stereochemistry of the enantioselective reductive alkylation of proline with ketones. Tetrahedron Asymmetry, 4, 331-338.
    • (1993) Tetrahedron Asymmetry, , vol.4 , pp. 331-338
    • Tóth, G.1    Kovàcs, A.2    Tarnai, T.3    Tungler, A.4
  • 149
    • 2442478134 scopus 로고    scopus 로고
    • Sonochemical asymmetric hydrogenation of isophorone on proline modified Pd/Al 2 O 3 catalysts
    • Mhadgut, S. C., Bucsi, I., Török, M., Török, B. (2004). Sonochemical asymmetric hydrogenation of isophorone on proline modified Pd/Al 2 O 3 catalysts. Chem. Commun., 984-985.
    • (2004) Chem. Commun., , pp. 984-985
    • Mhadgut, S.C.1    Bucsi, I.2    Török, M.3    Török, B.4
  • 150
    • 2342533023 scopus 로고    scopus 로고
    • In situ monitoring of catalytic three-phase enantio selective hydrogenation using FTIR/ATR spectroscopy
    • Pintar, A., Malacea, R., Pinel, C., Fogassy, G., Besson, M. (2004). In situ monitoring of catalytic three-phase enantio selective hydrogenation using FTIR/ATR spectroscopy. Appl. Catal. A, 264, 1-12.
    • (2004) Appl. Catal. A, , vol.264 , pp. 1-12
    • Pintar, A.1    Malacea, R.2    Pinel, C.3    Fogassy, G.4    Besson, M.5
  • 151
    • 32344448336 scopus 로고    scopus 로고
    • Highly asymmetric heterogeneous catalytic hydrogenation of isophorone on proline modified base - supported palladium catalysts
    • Mhadgut, S. C., Török, M., Esquibel, J., Török, B. (2006). Highly asymmetric heterogeneous catalytic hydrogenation of isophorone on proline modified base - supported palladium catalysts. J. Catal., 238, 441-448.
    • (2006) J. Catal , vol.238 , pp. 441-448
    • Mhadgut, S.C.1    Török, M.2    Esquibel, J.3    Török, B.4
  • 152
    • 33744939448 scopus 로고    scopus 로고
    • Heterogeneously catalyzed asymmetric C = C hydrogenation: origin of enantioselectivity in the proline-directed Pd/isophorone system
    • McIntosh, A. I., Watson, D. J., Burton, J. W., Lambert, R. M. (2006). Heterogeneously catalyzed asymmetric C = C hydrogenation: origin of enantioselectivity in the proline-directed Pd/isophorone system. J. Am. Chem. Soc., 128, 7329-7334.
    • (2006) J. Am. Chem. Soc., , vol.128 , pp. 7329-7334
    • McIntosh, A.I.1    Watson, D.J.2    Burton, J.W.3    Lambert, R.M.4
  • 153
    • 0029125708 scopus 로고
    • (-)-Dihydro-apovincaminic acid ethyl-ester, preparation and use as a chiral modifier in enantioselective heterogeneous catalytic hydrogenations
    • Tungler, A., Màth é, T., Tarnai, T., Fodor, K., Tóth, G., Kajtàr, J., Kolossvàry, I., Herényi, B., Sheldon, R. A. (1995). (-)-Dihydro-apovincaminic acid ethyl-ester, preparation and use as a chiral modifier in enantioselective heterogeneous catalytic hydrogenations. Tetrahedron Asymmetry, 6, 2395-2402.
    • (1995) Tetrahedron Asymmetry, , vol.6 , pp. 2395-2402
    • Tungler, A.1    Màthé, T.2    Tarnai, T.3    Fodor, K.4    Tóth, G.5    Kajtàr, J.6    Kolossvàry, I.7    Herényi, B.8    Sheldon, R.A.9
  • 155
    • 0035858737 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of isophorone over Pd catalysts in the presence of (-)-dihydroapovincaminic acid ethyl ester - the effect of reduction method of Pd blacks on the enantiomeric excess
    • Farkas, G., Sipos, E., Tungler, A., Sàrkàny, A., Figueiredo, J. L. (2001). Enantioselective hydrogenation of isophorone over Pd catalysts in the presence of (-)-dihydroapovincaminic acid ethyl ester - the effect of reduction method of Pd blacks on the enantiomeric excess. J. Mol. Catal. A Chem., 170, 101-107.
    • (2001) J. Mol. Catal. A Chem., , vol.170 , pp. 101-107
    • Farkas, G.1    Sipos, E.2    Tungler, A.3    Sàrkàny, A.4    Figueiredo, J.L.5
  • 156
    • 0037127504 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of isophorone with titania supported Pd catalysts modified by (-)-dihydroapovincaminic acid ethyl ester effect of the support and the reduction method
    • Sipos, E., Farkas, G., Tungler, A., Figueiredo, J. L. (2002). Enantioselective hydrogenation of isophorone with titania supported Pd catalysts modified by (-)-dihydroapovincaminic acid ethyl ester effect of the support and the reduction method. J. Mol. Catal. A Chem., 179, 107-112.
    • (2002) J. Mol. Catal. A Chem., , vol.179 , pp. 107-112
    • Sipos, E.1    Farkas, G.2    Tungler, A.3    Figueiredo, J.L.4
  • 157
    • 0033572861 scopus 로고    scopus 로고
    • Comparison of chiral modifiers in the Pd catalysed hydrogenation of phenylcinnamic acid and isophorone
    • Tungler, A., Nitta, Y., Fodor, K., Farkas, G., Màth é, T. (1999). Comparison of chiral modifiers in the Pd catalysed hydrogenation of phenylcinnamic acid and isophorone . J. Mol. Catal. A Chem., 149, 135-140.
    • (1999) J. Mol. Catal. A Chem., , vol.149 , pp. 135-140
    • Tungler, A.1    Nitta, Y.2    Fodor, K.3    Farkas, G.4    Màthé, T.5
  • 158
    • 0037158296 scopus 로고    scopus 로고
    • (S)-Alpha,alpha-diphenyl - and (S)-alpha,alpha-dinaphthyl-2-pyrrolidinemethanol as chiral modifiers in asymmetric heterogeneous catalytic hydrogenation of isophorone
    • Sipos, E., Tungler, A., Bitter, I., Kubinyi, M. (2002). (S)-Alpha,alpha-diphenyl - and (S)-alpha,alpha-dinaphthyl-2-pyrrolidinemethanol as chiral modifiers in asymmetric heterogeneous catalytic hydrogenation of isophorone. J. Mol. Catal. A Chem., 186, 187-192.
    • (2002) J. Mol. Catal. A Chem., , vol.186 , pp. 187-192
    • Sipos, E.1    Tungler, A.2    Bitter, I.3    Kubinyi, M.4
  • 160
    • 1242272764 scopus 로고    scopus 로고
    • Enantioselective hydrogenations with highly mesoporous carbon supported Pd catalysts
    • Sipos, E., Fogassy, G., Tungler, A., Samant, P. V., Figueiredo, J. L. (2004). Enantioselective hydrogenations with highly mesoporous carbon supported Pd catalysts. J. Mol. Catal. A Chem., 212, 245-250.
    • (2004) J. Mol. Catal. A Chem., , vol.212 , pp. 245-250
    • Sipos, E.1    Fogassy, G.2    Tungler, A.3    Samant, P.V.4    Figueiredo, J.L.5
  • 162
    • 0036167528 scopus 로고    scopus 로고
    • Heterogeneous enantioselective hydrogenation of 2-pyrones over cinchona-modified palladium
    • Huck, W. R., Mallat, T., Baiker, A. (2002). Heterogeneous enantioselective hydrogenation of 2-pyrones over cinchona-modified palladium. New J. Chem., 26, 6-8.
    • (2002) New J. Chem., , vol.26 , pp. 6-8
    • Huck, W.R.1    Mallat, T.2    Baiker, A.3
  • 163
    • 0000502313 scopus 로고    scopus 로고
    • Transient behavior of the enantioselective hydrogenation of a hydroxymethylpyrone
    • Huck, W. R., Mallat, T., Baiker, A. (2000). Transient behavior of the enantioselective hydrogenation of a hydroxymethylpyrone. Catal. Lett., 69, 129-132.
    • (2000) Catal. Lett., , vol.69 , pp. 129-132
    • Huck, W.R.1    Mallat, T.2    Baiker, A.3
  • 167
    • 0033235134 scopus 로고    scopus 로고
    • Enantio-differentiating hydrogenation of methyl 2-furoylacetate and its analogs over tartaric acid-modified Raney nickel
    • Nakagawa, S., Haruna, N., Acosta, D. E., Endo, T., Sugimura, T., Tai, A. (1999). Enantio-differentiating hydrogenation of methyl 2-furoylacetate and its analogs over tartaric acid-modified Raney nickel. Chem. Lett., 28, 1055-1056.
    • (1999) Chem. Lett., , vol.28 , pp. 1055-1056
    • Nakagawa, S.1    Haruna, N.2    Acosta, D.E.3    Endo, T.4    Sugimura, T.5    Tai, A.6
  • 168
    • 0347720697 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of furan-containing ketones over tartaric acid-modified Raney nickel catalyst
    • Haruna, N., Acosta, D. E., Nakagawa, S., Yamaguchi, K., Tai, A., Okuyama, T., Sugimura, T. (2004). Asymmetric hydrogenation of furan-containing ketones over tartaric acid-modified Raney nickel catalyst. Heterocycles, 62, 375-386.
    • (2004) Heterocycles, , vol.62 , pp. 375-386
    • Haruna, N.1    Acosta, D.E.2    Nakagawa, S.3    Yamaguchi, K.4    Tai, A.5    Okuyama, T.6    Sugimura, T.7
  • 169
    • 0141564594 scopus 로고    scopus 로고
    • Palladium-catalyzed asymmetric hydrogenation of furan carboxylic acids
    • Maris, M., Huck, W. R., Mallat, T., Baiker, A. (2003). Palladium-catalyzed asymmetric hydrogenation of furan carboxylic acids. J. Catal., 219, 52-58.
    • (2003) J. Catal., , vol.219 , pp. 52-58
    • Maris, M.1    Huck, W.R.2    Mallat, T.3    Baiker, A.4
  • 170
    • 0002585423 scopus 로고    scopus 로고
    • Potential and limitations of palladium - cinchona catalyst for the enantioselective hydrogenation of a hydroxymethylpyrone
    • Huck, W. R., Mallet, T., Baiker, A. (2000). Potential and limitations of palladium - cinchona catalyst for the enantioselective hydrogenation of a hydroxymethylpyrone . J. Catal., 193, 1-4.
    • (2000) J. Catal., , vol.193 , pp. 1-4
    • Huck, W.R.1    Mallet, T.2    Baiker, A.3
  • 171
    • 14344254792 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of aromatic ketones over cinchona-modified rhodium: a new opportunity? J
    • Sonderegger, O. J., Ho, G. M. W., Bürgi, T., Baiker, A. (2005). Enantioselective hydrogenation of aromatic ketones over cinchona-modified rhodium: a new opportunity? J. Catal., 230, 499-506.
    • (2005) Catal., , vol.230 , pp. 499-506
    • Sonderegger, O.J.1    Ho, G.M.W.2    Bürgi, T.3    Baiker, A.4
  • 173
    • 0000794832 scopus 로고    scopus 로고
    • Enantioselective hydrogenation of pyruvic acid oxime to alanine on Pd/alumina
    • Borszeky, K., Mallat, T., Aeschiman, R., Schweizer, W. B., Baiker, A. (1996). Enantioselective hydrogenation of pyruvic acid oxime to alanine on Pd/alumina. J. Catal., 161, 451-458.
    • (1996) J. Catal., , vol.161 , pp. 451-458
    • Borszeky, K.1    Mallat, T.2    Aeschiman, R.3    Schweizer, W.B.4    Baiker, A.5
  • 174
    • 0031042485 scopus 로고    scopus 로고
    • Progress in asymmetric heterogeneous catalysis: design of novel chirally modified platinum metal catalysts
    • Baiker, A. (1997). Progress in asymmetric heterogeneous catalysis: design of novel chirally modified platinum metal catalysts. J. Mol. Catal. A Chem., 115, 473-493.
    • (1997) J. Mol. Catal. A Chem., , vol.115 , pp. 473-493
    • Baiker, A.1
  • 176
    • 0242299266 scopus 로고    scopus 로고
    • Interaction between ketopantolactone and chirally modified Pt investigated by attenuated total reflection IR concentration modulation spectroscopy
    • Bonalumi, N., Burgi, T., Baiker, A. (2003). Interaction between ketopantolactone and chirally modified Pt investigated by attenuated total reflection IR concentration modulation spectroscopy. J. Am. Chem. Soc., 125, 13342-13343.
    • (2003) J. Am. Chem. Soc., , vol.125 , pp. 13342-13343
    • Bonalumi, N.1    Burgi, T.2    Baiker, A.3
  • 177
    • 4244018872 scopus 로고    scopus 로고
    • Design of new modifiers for the enantioselective hydrogenation of ethyl pyruvate
    • Schurch, M., Heinz, T., Aeschimann, R., Mallat, T., Pfaltz, A., Baiker, A. (1998). Design of new modifiers for the enantioselective hydrogenation of ethyl pyruvate . J. Catal., 173, 187-195.
    • (1998) J. Catal., , vol.173 , pp. 187-195
    • Schurch, M.1    Heinz, T.2    Aeschimann, R.3    Mallat, T.4    Pfaltz, A.5    Baiker, A.6
  • 179
    • 0000451702 scopus 로고
    • Enantioselective hydrogenation of alpha-ketoesters over Pt/alumina modified with cinchonidine - theoretical investigation of the substrate-modifier interaction
    • Schwalm, O., Minder, B., Weber, J., Baiker, A. (1994). Enantioselective hydrogenation of alpha-ketoesters over Pt/alumina modified with cinchonidine - theoretical investigation of the substrate-modifier interaction. Catal. Lett., 23, 271-279.
    • (1994) Catal. Lett., , vol.23 , pp. 271-279
    • Schwalm, O.1    Minder, B.2    Weber, J.3    Baiker, A.4
  • 180
    • 0000361784 scopus 로고
    • Ab-initio and semiempirical investigations of the complexation of methyl pyruvate by ammonia and the ammonium cation
    • Schwalm, O., Weber, J., Margitfalvi, J., Baiker, A. (1993). Ab-initio and semiempirical investigations of the complexation of methyl pyruvate by ammonia and the ammonium cation. J. Mol. Struct., 297, 285-293.
    • (1993) J. Mol. Struct., , vol.297 , pp. 285-293
    • Schwalm, O.1    Weber, J.2    Margitfalvi, J.3    Baiker, A.4
  • 181
    • 84987141375 scopus 로고
    • Theoretical investigation of the enantioselective hydrogenation of alpha-ketoesters over Pt alumina modified with cinchonidine
    • Schwalm, O., Weber, J., Minder, B., Baiker, A. (1994). Theoretical investigation of the enantioselective hydrogenation of alpha-ketoesters over Pt alumina modified with cinchonidine. Int. J. Quantum Chem., 52, 191-197.
    • (1994) Int. J. Quantum Chem., , vol.52 , pp. 191-197
    • Schwalm, O.1    Weber, J.2    Minder, B.3    Baiker, A.4
  • 182
  • 183
    • 0040805975 scopus 로고    scopus 로고
    • Model for enantioselective hydrogenation of alpha - ketoesters over chirally modified platinum revisited: influence of alpha-ketoester conformation
    • Burgi, T., Baiker, A. (2000). Model for enantioselective hydrogenation of alpha - ketoesters over chirally modified platinum revisited: influence of alpha-ketoester conformation. J. Catal., 194, 445-451.
    • (2000) J. Catal., , vol.194 , pp. 445-451
    • Burgi, T.1    Baiker, A.2
  • 184
    • 0035742813 scopus 로고    scopus 로고
    • Model of reactant-modifier interaction in enantioselective hydrogenation of ethyl pyruvate on platinum-cinchona catalysts: extension to synthetic chiral modifiers
    • Vargas, A., Burgi, T., Baiker, A. (2001). Model of reactant-modifier interaction in enantioselective hydrogenation of ethyl pyruvate on platinum-cinchona catalysts: extension to synthetic chiral modifiers. J. Catal., 197, 378-384.
    • (2001) J. Catal., , vol.197 , pp. 378-384
    • Vargas, A.1    Burgi, T.2    Baiker, A.3
  • 185
    • 0036301619 scopus 로고    scopus 로고
    • Origin of the rate acceleration in enantioselective hydrogenation of alpha-functionalised ketones over cinchona alkaloid modified platinum
    • Vargas, A., Burgi, T., Baiker, A. (2002). Origin of the rate acceleration in enantioselective hydrogenation of alpha-functionalised ketones over cinchona alkaloid modified platinum. New J. Chem., 26, 807-810.
    • (2002) New J. Chem., , vol.26 , pp. 807-810
    • Vargas, A.1    Burgi, T.2    Baiker, A.3
  • 186
    • 0037173408 scopus 로고    scopus 로고
    • Relation between electronic structure of alpha-substituted ketones and their reactivity in racemic and enantioselective platinum-catalyzed hydrogenation
    • Vargas, A., Bürgi, T., von Arx, M., Hess, R., Baiker, A. (2002). Relation between electronic structure of alpha-substituted ketones and their reactivity in racemic and enantioselective platinum-catalyzed hydrogenation. J. Catal., 209, 489-500.
    • (2002) J. Catal., , vol.209 , pp. 489-500
    • Vargas, A.1    Bürgi, T.2    von Arx, M.3    Hess, R.4    Baiker, A.5
  • 187
    • 67849114704 scopus 로고    scopus 로고
    • Experimental and theoretical analysis of asymmetric induction in heterogeneous catalysis: diastereoselective hydrogenation of chiral alpha - hydroxyketones over Pt catalyst
    • Busygin, I., Taskinen, A., Nieminen, V., Toukoniitty, E., Stillger, T., Leino, R., Murzin, D. Y. (2009). Experimental and theoretical analysis of asymmetric induction in heterogeneous catalysis: diastereoselective hydrogenation of chiral alpha - hydroxyketones over Pt catalyst. J. Am. Chem. Soc., 131, 4449-4462.
    • (2009) J. Am. Chem. Soc., , vol.131 , pp. 4449-4462
    • Busygin, I.1    Taskinen, A.2    Nieminen, V.3    Toukoniitty, E.4    Stillger, T.5    Leino, R.6    Murzin, D.Y.7
  • 188
    • 28844463872 scopus 로고    scopus 로고
    • One-to-one reactant-modifier interactions in enantio-and diastereoselective hydrogenation of chiral alpha-hydroxyketones on Pt(111)
    • Nieminen, V., Taskinen, A., Toukonitty, E., Hotokka, M., Murzin, D. Y. (2006). One-to-one reactant-modifier interactions in enantio-and diastereoselective hydrogenation of chiral alpha-hydroxyketones on Pt(111). J. Catal., 237, 131-142.
    • (2006) J. Catal., , vol.237 , pp. 131-142
    • Nieminen, V.1    Taskinen, A.2    Toukonitty, E.3    Hotokka, M.4    Murzin, D.Y.5
  • 189
    • 17344362318 scopus 로고    scopus 로고
    • Ab initio study of solvent effects on reactant - modifier complexes in enantioselective hydrogenation
    • Taskinen, A., Toukoniitty, E. (2005). Ab initio study of solvent effects on reactant - modifier complexes in enantioselective hydrogenation. Catal. Today., 100, 373-377.
    • (2005) Catal. Today., , vol.100 , pp. 373-377
    • Taskinen, A.1    Toukoniitty, E.2
  • 190
    • 2342620623 scopus 로고    scopus 로고
    • A combined experimental and theoretical study of 1-phenylpropane - 1,2-dione hydrogenation over heterogeneous cinchonidine-modified Pt catalyst
    • Toukoniitty, E., Nieminen, V., Taskinen, A., Paivarinta, J., Hotokka, M., Murzin, D. Y. (2004). A combined experimental and theoretical study of 1-phenylpropane - 1,2-dione hydrogenation over heterogeneous cinchonidine-modified Pt catalyst. J. Catal., 224, 326-339.
    • (2004) J. Catal., , vol.224 , pp. 326-339
    • Toukoniitty, E.1    Nieminen, V.2    Taskinen, A.3    Paivarinta, J.4    Hotokka, M.5    Murzin, D.Y.6
  • 191
    • 0015101706 scopus 로고
    • Entropic contributions to rate accelerations in enzymic and intramolecular reactions and chelate effect
    • Page, M. I., Jencks, W. P. (1971). Entropic contributions to rate accelerations in enzymic and intramolecular reactions and chelate effect. Proc. Natl. Acad. Sci. U.S.A., 68, 1678.
    • (1971) Proc. Natl. Acad. Sci. U.S.A. , vol.68 , pp. 1678
    • Page, M.I.1    Jencks, W.P.2
  • 192
    • 49249092240 scopus 로고    scopus 로고
    • Chiral recognition on catalytic surfaces: theoretical insight in a biomimetic heterogeneous catalytic system
    • Vargas, A., Santarossa, G., Iannuzzi, M., Baiker, A. (2008). Chiral recognition on catalytic surfaces: theoretical insight in a biomimetic heterogeneous catalytic system. J. Phys. Chem. C, 112, 10200-10208.
    • (2008) J. Phys. Chem. C, , vol.112 , pp. 10200-10208
    • Vargas, A.1    Santarossa, G.2    Iannuzzi, M.3    Baiker, A.4
  • 193
    • 0025673823 scopus 로고
    • Conformational study of cinchona alkaloids - a combined NMR and molecular-orbital approach
    • Dijkstra, G. D. H., Kellogg, R. M., Wynberg, H. (1990). Conformational study of cinchona alkaloids - a combined NMR and molecular-orbital approach. J. Org. Chem., 55, 6121-6131.
    • (1990) J. Org. Chem., , vol.55 , pp. 6121-6131
    • Dijkstra, G.D.H.1    Kellogg, R.M.2    Wynberg, H.3
  • 194
    • 0024343737 scopus 로고
    • Conformational study of cinchona alkaloids - a combined NMR, molecular mechanics, and X-ray approach
    • Dijkstra, G. D. H., Kellogg, R. M., Wynberg, H., Svendsen, J. S., Marko, I., Sharpless, K. B. (1989). Conformational study of cinchona alkaloids - a combined NMR, molecular mechanics, and X-ray approach. J. Am. Chem. Soc., 111, 8069-8076.
    • (1989) J. Am. Chem. Soc., , vol.111 , pp. 8069-8076
    • Dijkstra, G.D.H.1    Kellogg, R.M.2    Wynberg, H.3    Svendsen, J.S.4    Marko, I.5    Sharpless, K.B.6
  • 195
    • 0032539230 scopus 로고    scopus 로고
    • Conformational behavior of cinchonidine in different solvents: a combined NMR and ab initio investigation
    • Burgi, T., Baiker, A. (1998). Conformational behavior of cinchonidine in different solvents: a combined NMR and ab initio investigation. J. Am. Chem. Soc., 120, 12920-12926.
    • (1998) J. Am. Chem. Soc., , vol.120 , pp. 12920-12926
    • Burgi, T.1    Baiker, A.2
  • 196
    • 49649129660 scopus 로고    scopus 로고
    • Conformational behavior of cinchonidine revisited: a combined theoretical and experimental study
    • Urakawa, A., Meier, D. M., Rugger, H., Baiker, A. (2008). Conformational behavior of cinchonidine revisited: a combined theoretical and experimental study. J. Phys. Chem. A, 112, 7250-7255.
    • (2008) J. Phys. Chem. A, , vol.112 , pp. 7250-7255
    • Urakawa, A.1    Meier, D.M.2    Rugger, H.3    Baiker, A.4
  • 197
    • 0035814410 scopus 로고    scopus 로고
    • An in situ attenuated total reflection infrared study of a chiral catalytic solid-liquid interface: cinchonidine adsorption on Pt
    • Ferri, D., Burgi, T. (2001). An in situ attenuated total reflection infrared study of a chiral catalytic solid-liquid interface: cinchonidine adsorption on Pt. J. Am. Chem. Soc., 123, 12074-12084.
    • (2001) J. Am. Chem. Soc., , vol.123 , pp. 12074-12084
    • Ferri, D.1    Burgi, T.2
  • 198
    • 0035822457 scopus 로고    scopus 로고
    • Chiral modification of platinum catalysts by cinchonidine adsorption studied by in situ ATR-IR spectroscopy
    • Ferri, D., Burgi, T., Baiker, A. (2001). Chiral modification of platinum catalysts by cinchonidine adsorption studied by in situ ATR-IR spectroscopy. Chem. Commun., 1172-1173.
    • (2001) Chem. Commun., , pp. 1172-1173
    • Ferri, D.1    Burgi, T.2    Baiker, A.3
  • 199
    • 33644856259 scopus 로고    scopus 로고
    • First principles study of the conformations of cinchonidine on a Pt(111) surface
    • Vargas, A., Baiker, A. (2006). First principles study of the conformations of cinchonidine on a Pt(111) surface. J. Catal., 239, 220-226.
    • (2006) J. Catal., , vol.239 , pp. 220-226
    • Vargas, A.1    Baiker, A.2
  • 200
    • 3242680436 scopus 로고    scopus 로고
    • Adsorption of cinchonidine on platinum: a DFT insight in the mechanism of enantioselective hydrogenation of activated ketones
    • Vargas, A., Burgi, T., Baiker, A. (2004). Adsorption of cinchonidine on platinum: a DFT insight in the mechanism of enantioselective hydrogenation of activated ketones. J. Catal., 226, 69-82.
    • (2004) J. Catal., , vol.226 , pp. 69-82
    • Vargas, A.1    Burgi, T.2    Baiker, A.3
  • 201
    • 0032495030 scopus 로고    scopus 로고
    • A new cinchona-modified platinum catalyst for the enantioselective hydrogenation of pyruvate: the structure of the 1:1 alkaloid-reactant complex
    • Bartok, M., Felfoldi, K., Torok, B., Bartok, T. (1998). A new cinchona-modified platinum catalyst for the enantioselective hydrogenation of pyruvate: the structure of the 1:1 alkaloid-reactant complex. Chem. Commun., 2605-2606.
    • (1998) Chem. Commun., , pp. 2605-2606
    • Bartok, M.1    Felfoldi, K.2    Torok, B.3    Bartok, T.4
  • 202
    • 33644856259 scopus 로고    scopus 로고
    • First principles study of the conformations of cinchonidine on a Pt(111) surface
    • Vargas, A., Baiker, A. (2006). First principles study of the conformations of cinchonidine on a Pt(111) surface. J. Catal., 239, 220-226.
    • (2006) J. Catal., , vol.239 , pp. 220-226
    • Vargas, A.1    Baiker, A.2
  • 203
    • 27644434346 scopus 로고    scopus 로고
    • DFT and ATR-IR insight into the conformational flexibility of cinchonidine adsorbed on platinum: proton exchange with metal
    • Vargas, A., Ferri, D., Baiker, A. (2005). DFT and ATR-IR insight into the conformational flexibility of cinchonidine adsorbed on platinum: proton exchange with metal. J. Catal., 236, 1-8.
    • (2005) J. Catal., , vol.236 , pp. 1-8
    • Vargas, A.1    Ferri, D.2    Baiker, A.3
  • 204
    • 47249164765 scopus 로고    scopus 로고
    • Chiral modification of Rh and Pt surfaces: effect of rotational flexibility of cinchona-type modifiers on their adsorption behavior
    • Schmidt, E., Ferri, D., Vargas, A., Baiker, A. (2008). Chiral modification of Rh and Pt surfaces: effect of rotational flexibility of cinchona-type modifiers on their adsorption behavior. J. Phys. Chem. C, 112, 3866-3874.
    • (2008) J. Phys. Chem. C, , vol.112 , pp. 3866-3874
    • Schmidt, E.1    Ferri, D.2    Vargas, A.3    Baiker, A.4
  • 205
    • 36549041885 scopus 로고    scopus 로고
    • Chirally modified platinum generated by adsorption of cinchonidine ether derivatives: towards uncovering the chiral sites
    • Bonalumi, N., Vargas, A., Ferri, D., Baiker, A. (2007). Chirally modified platinum generated by adsorption of cinchonidine ether derivatives: towards uncovering the chiral sites. Chem. Eur. J., 13, 9236-9244.
    • (2007) Chem. Eur. J., , vol.13 , pp. 9236-9244
    • Bonalumi, N.1    Vargas, A.2    Ferri, D.3    Baiker, A.4
  • 206
    • 34547478249 scopus 로고    scopus 로고
    • Catalytic chiral metal surfaces generated by adsorption of O-Phenyl derivatives of cinchonidine
    • Bonalumi, N., Vargas, A., Ferri, D., Baiker, A. (2007). Catalytic chiral metal surfaces generated by adsorption of O-Phenyl derivatives of cinchonidine. J. Phys. Chem. C., 111, 9349-9358.
    • (2007) J. Phys. Chem. C., , vol.111 , pp. 9349-9358
    • Bonalumi, N.1    Vargas, A.2    Ferri, D.3    Baiker, A.4
  • 207
    • 34250737412 scopus 로고    scopus 로고
    • Controlling the sense of enantioselection on surfaces by conformational changes of adsorbed modifiers
    • Vargas, A., Ferri, D., Bonalumi, N., Mallat, T., Baiker, A. (2007). Controlling the sense of enantioselection on surfaces by conformational changes of adsorbed modifiers. Angew. Chem. Int. Ed., 46, 3905-3908.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 3905-3908
    • Vargas, A.1    Ferri, D.2    Bonalumi, N.3    Mallat, T.4    Baiker, A.5
  • 208
    • 6344256585 scopus 로고    scopus 로고
    • Fine tuning the "chiral sites" on solid enantio selective catalysts
    • Diezi, S., Mallat, T., Szabo, A., Baiker, A. (2004). Fine tuning the "chiral sites" on solid enantio selective catalysts. J. Catal., 228, 162-173.
    • (2004) J. Catal., , vol.228 , pp. 162-173
    • Diezi, S.1    Mallat, T.2    Szabo, A.3    Baiker, A.4
  • 209
    • 0042331941 scopus 로고    scopus 로고
    • Inversion of enantioselectivity in the hydrogenation of ketopantolactone on platinum modified by ether derivatives of cinchonidine
    • Diezi, S., Szabo, A., Mallat, T., Baiker, A. (2003). Inversion of enantioselectivity in the hydrogenation of ketopantolactone on platinum modified by ether derivatives of cinchonidine. Tetrahedron Asymmetry, 14, 2573-2577.
    • (2003) Tetrahedron Asymmetry, , vol.14 , pp. 2573-2577
    • Diezi, S.1    Szabo, A.2    Mallat, T.3    Baiker, A.4
  • 210
    • 34548240790 scopus 로고    scopus 로고
    • Role of guiding groups in cinchona-modified platinum for controlling the sense of enantiodifferentiation in the hydrogenation of ketones
    • Hoxha, F., Konigsmann, L., Vargas, A., Ferri, D., Mallat, T., Baiker, A. (2007). Role of guiding groups in cinchona-modified platinum for controlling the sense of enantiodifferentiation in the hydrogenation of ketones. J. Am. Chem. Soc., 129, 10582-10590.
    • (2007) J. Am. Chem. Soc., , vol.129 , pp. 10582-10590
    • Hoxha, F.1    Konigsmann, L.2    Vargas, A.3    Ferri, D.4    Mallat, T.5    Baiker, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.