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Volumn 15, Issue 4, 2010, Pages 2166-2177

Selective heck arylation of cyclohexene with homogeneous and heterogeneous palladium catalysts

Author keywords

Cyclohexene; Heck coupling; Heterogenized catalysts; Palladium

Indexed keywords

4 PHENYLCYCLOHEXENE; 4-PHENYLCYCLOHEXENE; ACETIC ACID DERIVATIVE; ALUMINUM OXIDE; CYCLOHEXANE DERIVATIVE; CYCLOHEXENE; CYCLOHEXENE DERIVATIVE; IODOBENZENE; ORGANOMETALLIC COMPOUND; PALLADIUM; PALLADIUM CHLORIDE; PALLADIUM(II) ACETATE;

EID: 77951872184     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15042166     Document Type: Article
Times cited : (19)

References (49)
  • 1
    • 4444264948 scopus 로고
    • Palladium-catalyzed reactions of organic halides with olefins
    • Heck, R.F. Palladium-catalyzed reactions of organic halides with olefins. Acc. Chem. Res. 1979, 12, 146-151.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 146-151
    • Heck, R.F.1
  • 2
    • 0034249671 scopus 로고    scopus 로고
    • The heck reaction as a sharpening stone of palladium catalysis
    • Beletskaya, I.P.; Cherpakov, A.V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100, 3009-3066.
    • (2000) Chem. Rev. , vol.100 , pp. 3009-3066
    • Beletskaya, I.P.1    Cherpakov, A.V.2
  • 3
    • 0035959456 scopus 로고    scopus 로고
    • Advances in the Heck chemistry of aryl bromides and chlorides
    • Whitcombe, N.J.; Hii, K.K.; Gibson, S.E. Advances in the Heck chemistry of aryl bromides and chlorides. Tetrahedron 2001, 57, 7449-7476.
    • (2001) Tetrahedron , vol.57 , pp. 7449-7476
    • Whitcombe, N.J.1    Hii, K.K.2    Gibson, S.E.3
  • 4
    • 27644586832 scopus 로고    scopus 로고
    • Structural and mechanistic studies of Pd-catalyzed C-C bond formation: The case of carbonylation and Heck reaction
    • Trzeciak, AM.; Ziółkowski, J.J. Structural and mechanistic studies of Pd-catalyzed C-C bond formation: The case of carbonylation and Heck reaction. Coord. Chem. Rev. 2005, 249, 2308-2322.
    • (2005) Coord. Chem. Rev. , vol.249 , pp. 2308-2322
    • Trzeciak, A.M.1    Ziółkowski, J.J.2
  • 5
    • 84985940921 scopus 로고    scopus 로고
    • Palladium reagents and catalysts
    • John Wiley & Sons, Ltd.: Chichester, West Sussex, UK
    • Tsuji, I. Palladium Reagents and Catalysts. In New Perspectives for the 21 st Century. John Wiley & Sons, Ltd.: Chichester, West Sussex, UK, 2004; pp. 105-176.
    • (2004) New Perspectives for the 21 St Century , pp. 105-176
    • Tsuji, I.1
  • 6
    • 9744246801 scopus 로고    scopus 로고
    • The development of palladium catalysts for C-C and Cheteroatom bond forming reactions of aryl chloride substrates
    • Bedford, R.B.; Cazin, C.S.J.; Holder, D. The development of palladium catalysts for C-C and Cheteroatom bond forming reactions of aryl chloride substrates. Coord. Chem. Rev. 2004, 248, 2283-2321.
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 2283-2321
    • Bedford, R.B.1    Cazin, C.S.J.2    Holder, D.3
  • 7
    • 9644254490 scopus 로고    scopus 로고
    • Recent homogeneous catalytic applications of chelate and pincer nheterocyclic carbenes
    • Peris, E.; Crabtree, R.H. Recent homogeneous catalytic applications of chelate and pincer Nheterocyclic carbenes. Coord. Chem. Rev. 2004, 248, 2239-2246.
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 2239-2246
    • Peris, E.1    Crabtree, R.H.2
  • 8
    • 13444291493 scopus 로고    scopus 로고
    • Pd-PVP colloid as catalyst for Heck and carbonylation reactions: TEM and XPS studies
    • DOI 10.1016/j.jcat.2004.11.003, PII S0021951704005354
    • Gniewek, A.; Trzeciak, A.M.; Ziółkowski, J.J.; Kȩpíski, L.; Wrzyszcz, J.; Tylus, W. Pd-PVP colloid as catalyst for Heck and carbonylation reactions: TEM and XPS studies. J. Catal. 2005, 229, 332-343. (Pubitemid 40215177)
    • (2005) Journal of Catalysis , vol.229 , Issue.2 , pp. 332-343
    • Gniewek, A.1    Trzeciak, A.M.2    Ziolkowski, J.J.3    Kepinski, L.4    Wrzyszcz, J.5    Tylus, W.6
  • 9
    • 0034598519 scopus 로고    scopus 로고
    • Phosphane-free palladium-catalyzed coupling reactions: The decisive role of Pd nanoparticles
    • DOI 10.1002/(SICI)1521-3773(20000103)39:1<165::AID-ANIE165>3.0. CO;2-B
    • Reetz, M.T.; Westermann, E. Phosphane-Free Palladium-Catalyzed Coupling Reactions: The Decisive Role of Pd Nanoparticles. Angew. Chem. Int. Ed. 2000, 39, 165-168. (Pubitemid 30265703)
    • (2000) Angewandte Chemie - International Edition , vol.39 , Issue.1 , pp. 165-168
    • Reetz, M.T.1    Westermann, E.2
  • 10
    • 0037419139 scopus 로고    scopus 로고
    • Pd nanoparticles catalyzed stereospecific synthesis of β-aryl cinnamic esters in ionic liquids
    • DOI 10.1021/jo026877t
    • Calo, V.; Nacci, A.; Monopoli, A.; Laera, S.; Cioffi, N. Pd Nanoparticles Catalyzed Stereospecific Synthesis of β-Aryl Cinnamic Esters in Ionic Liquids. J. Org. Chem. 2003, 68, 2929-2933. (Pubitemid 36519130)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.7 , pp. 2929-2933
    • Calo, V.1    Nacci, A.2    Monopoli, A.3    Laera, S.4    Cioffi, N.5
  • 11
    • 33748320799 scopus 로고    scopus 로고
    • Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide
    • DOI 10.1016/j.molcata.2006.03.064, PII S1381116906007151
    • Pryjomska-Ray, I.; Trzeciak, A.M.; Ziółkowski, J.J. Base free efficient palladium catalysts of Heck reaction in molten tetrabutylammonium bromide. J. Mol. Catal. A: Chem. 2006, 257, 3-8. (Pubitemid 44332302)
    • (2006) Journal of Molecular Catalysis A: Chemical , vol.257 , Issue.1-2 , pp. 3-8
    • Pryjomska-Ray, I.1    Trzeciak, A.M.2    Ziolkowski, J.J.3
  • 12
    • 34547338866 scopus 로고    scopus 로고
    • N-heterocyclic carbenes in transition metal catalysis
    • Glorius, F., Eds.; Springer-Verlag: Berlin, Heidelberg, New York, NY, USA
    • Glorius, F. N-heterocyclic carbenes in transition metal catalysis. In Top. Organomet. Chem., Glorius, F., Eds.; Springer-Verlag: Berlin, Heidelberg, New York, NY, USA, 2007; Volume 3, pp. 1-218.
    • (2007) Top. Organomet. Chem. , vol.3 , pp. 1-218
    • Glorius, F.1
  • 13
    • 84889439715 scopus 로고    scopus 로고
    • Cross-coupling reactions catalyzed by palladium N-heterocyclic carbene complexes
    • Nolan, S.P., Ed.; Wiley-VCH: Weinheim, Germany
    • Scott, M.N.; Nolan, S.P. Cross-coupling reactions catalyzed by palladium N-heterocyclic carbene complexes. In N-heterocyclic Carbenes in Synthesis; Nolan, S.P., Ed.; Wiley-VCH: Weinheim, Germany, 2006; pp. 55-70.
    • (2006) N-heterocyclic Carbenes in Synthesis , pp. 55-70
    • Scott, M.N.1    Nolan, S.P.2
  • 14
    • 0042975158 scopus 로고    scopus 로고
    • Formation of carbon-carbon bonds under catalysis by transitionmetal nanoparticles
    • Moreno-Manas, M.; Pleixats, R. Formation of carbon-carbon bonds under catalysis by transitionmetal nanoparticles. Acc. Chem. Res. 2003, 36, 638-643.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 638-643
    • Moreno-Manas, M.1    Pleixats, R.2
  • 15
    • 33847019589 scopus 로고    scopus 로고
    • Monomolecular, nanosized and heterogenized palladium catalysts for the heck reaction
    • Trzeciak, A.M.; Ziółkowski, J.J. Monomolecular, nanosized and heterogenized palladium catalysts for the Heck reaction. Coord. Chem. Rev. 2007, 251, 1281-1293.
    • (2007) Coord. Chem. Rev. , vol.251 , pp. 1281-1293
    • Trzeciak, A.M.1    Ziółkowski, J.J.2
  • 16
    • 60649093462 scopus 로고    scopus 로고
    • Palladium nanoparticles supported on polyvinylpyridine: Catalytic activity in Heck-type reactions and XPS structural studies
    • Evangelisti, C.; Panziera, N.; Petrici, P.; Vitulli, G.; Salvadori, P.; Battocchio, C.; Polzonetti, G. Palladium nanoparticles supported on polyvinylpyridine: Catalytic activity in Heck-type reactions and XPS structural studies. J. Catal. 2009, 262, 287-293.
    • (2009) J. Catal. , vol.262 , pp. 287-293
    • Evangelisti, C.1    Panziera, N.2    Petrici, P.3    Vitulli, G.4    Salvadori, P.5    Battocchio, C.6    Polzonetti, G.7
  • 17
    • 0035833117 scopus 로고    scopus 로고
    • Arylation of α-substituted acrylates in ionic liquids catalyzed by a Pd-benzothiazole carbene complex
    • DOI 10.1016/S0040-4039(01)00795-X, PII S004040390100795X
    • Calo, V.; Nacci, A.; Lopez, L.; Napoli, A. Arylation of α-substituted acrylates in ionic liquids catalyzed by a Pd-benzothiazole carbene complex. Tetrahedron Lett. 2001, 42, 4701-4703. (Pubitemid 32553802)
    • (2001) Tetrahedron Letters , vol.42 , Issue.28 , pp. 4701-4703
    • Calo, V.1    Nacci, A.2    Lopez, L.3    Napola, A.4
  • 18
    • 0034638784 scopus 로고    scopus 로고
    • Heck reaction in ionic liquids catalyzed by a Pd- benzothiazole carbene complex
    • Calo, V.; Nacci, A.; Lopez, L.; Mannarini, N. Heck reaction in ionic liquids catalyzed by a Pd- benzothiazole carbene complex. Tetrahedron Lett. 2000, 41, 8973-8976.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8973-8976
    • Calo, V.1    Nacci, A.2    Lopez, L.3    Mannarini, N.4
  • 19
    • 0028236671 scopus 로고
    • Tetraalkylammonium salts in Heck-type reactions using an alkali metal hydrogen carbonate or an alkali metal acetate as the base
    • DOI 10.1016/S0040-4039(00)73124-8
    • Jeffery, T.; Galland, J.-C. Tetraalkylammonium salts in Heck-type reactions using an alkali-metal hydrogen carbonate or an alkali-metal acetate as the base. Tetrahedron Lett. 1994, 35, 4101-4106. (Pubitemid 24194968)
    • (1994) Tetrahedron Letters , vol.35 , Issue.24 , pp. 4103-4106
    • Jeffery, T.1    Galland, J.-C.2
  • 20
    • 0032490909 scopus 로고    scopus 로고
    • Catalyst systems for directing heck-type reactions
    • [Pd/Base/QX]
    • Jeffery, T.; David, M. [Pd/Base/QX] catalyst systems for directing Heck-type reactions. Tetrahedron Lett. 1998, 39, 5751-5754.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5751-5754
    • Jeffery, T.1    David, M.2
  • 21
    • 0035029450 scopus 로고    scopus 로고
    • Metallic palladium in the heck reaction: Active catalyst or convenient precursor?
    • Biffis, A.; Zecca, M.; Basato, M. Metallic palladium in the Heck reaction: active catalyst or convenient precursor? Eur. J. Chem. 2001, 5, 1131-1133. (Pubitemid 32397274)
    • (2001) European Journal of Inorganic Chemistry , Issue.5 , pp. 1131-1133
    • Biffis, A.1    Zecca, M.2    Basato, M.3
  • 22
    • 84896690987 scopus 로고    scopus 로고
    • Homogeneous/heterogenous palladium based catalytic system for Heck reaction. the reversible transfer of palladium between solution and support
    • Pryjomska-Ray, I.; Gniewek, A.; Trzeciak, A.M.; Ziółkowski, J.J.; Tylus, W. Homogeneous/heterogenous palladium based catalytic system for Heck reaction. The reversible transfer of palladium between solution and support. Topics Catal. 2006, 40, 173-184.
    • (2006) Topics Catal. , vol.40 , pp. 173-184
    • Pryjomska-Ray, I.1    Gniewek, A.2    Trzeciak, A.M.3    Ziółkowski, J.J.4    Tylus, W.5
  • 23
    • 3142613268 scopus 로고    scopus 로고
    • In situ generation of highly active dissolved palladium species from solid catalysts - A concept for the activation of aryl chlorides in the heck reaction
    • DOI 10.1002/anie.200353473
    • Pröckl, S.S.; Kleist, W.; Gruber, M.A.; Köhler, K. In situ generation of highly active dissolved palladium species from solid catalysts - a concept for the activation of aryl chlorides in the Heck reaction. Angew. Chem. Int. Ed. 2004, 43, 1881-1882. (Pubitemid 39257850)
    • (2004) Angewandte Chemie - International Edition , vol.43 , Issue.14 , pp. 1881-1882
    • Prockl, S.S.1    Kleist, W.2    Gruber, M.A.3    Kohler, K.4
  • 24
    • 58249103006 scopus 로고    scopus 로고
    • Pd/MOx materials synthesized by sol-gel coprecipitation as catalysts for carbon-carbon coupling reactions of aryl bromides and chlorides
    • Kleist, W.; Lee, J.-K.; Köhler, K. Pd/MOx materials synthesized by sol-gel coprecipitation as catalysts for carbon-carbon coupling reactions of aryl bromides and chlorides. Eur. J. Inorg. Chem. 2009, 2, 261-266.
    • (2009) Eur. J. Inorg. Chem. , vol.2 , pp. 261-266
    • Kleist, W.1    Lee, J.-K.2    Köhler, K.3
  • 25
    • 0035866481 scopus 로고    scopus 로고
    • Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis
    • PII S0920586100006106
    • Köhler, K.; Wagner, M.; Djakovitch, L. Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis. Catal. Today 2001, 66, 105-114. (Pubitemid 32287742)
    • (2001) Catalysis Today , vol.66 , Issue.1 , pp. 105-114
    • Kohler, K.1    Wagner, M.2    Djakovitch, L.3
  • 26
    • 24344446504 scopus 로고    scopus 로고
    • Design of highly active heterogeneous palladium catalysts for the activation of aryl chlorides in Heck reactions
    • DOI 10.1016/j.tet.2005.06.111, PII S0040402005010823, Development and Application of Highly Active and Selective Palladium Catalysts
    • Pröckl, S.S.; Kleist, W.; Köhler, K. Design of highly active heterogeneous palladium catalysts for the activation of aryl chlorides in Heck reactions. Tetrahedron 2005, 61, 9855-9859. (Pubitemid 41262064)
    • (2005) Tetrahedron , vol.61 , Issue.41 , pp. 9855-9859
    • Prockl, S.S.1    Kleist, W.2    Kohler, K.3
  • 27
    • 70349226817 scopus 로고    scopus 로고
    • Silica-supported palladium: Sustainable catalysts for crosscoupling reactions
    • Polshettiwar, V.; Len, C.; Fihri, A. Silica-supported palladium: sustainable catalysts for crosscoupling reactions. Coord. Chem. Rev. 2009, 253, 2599-2626.
    • (2009) Coord. Chem. Rev. , vol.253 , pp. 2599-2626
    • Polshettiwar, V.1    Len, C.2    Fihri, A.3
  • 28
    • 34250157778 scopus 로고    scopus 로고
    • Silica-supported Pd catalysts for Heck coupling reactions
    • DOI 10.1016/j.tet.2007.04.023, PII S0040402007006424
    • Polshettiwar, V.; Molnar, A. Silica-supported Pd catalysts for Heck coupling reactions. Tetrahedron 2007, 63, 6949-6976. (Pubitemid 46894725)
    • (2007) Tetrahedron , vol.63 , Issue.30 , pp. 6949-6976
    • Polshettiwar, V.1    Molnar, A.2
  • 29
    • 0002598603 scopus 로고    scopus 로고
    • Heck reactions between aryl halides and olefins catalysed by Pd-complexes entrapped into zeolites NaY
    • PII S0022328X99000807
    • Djakovitch, L.; Heise, H.; Köhler, K. Heck reactions between aryl halides and olefins catalysed by Pd-complexes entrapped into zeolites NaY. J. Organomet. Chem. 1999, 584, 16-26. (Pubitemid 129610980)
    • (1999) Journal of Organometallic Chemistry , vol.584 , Issue.1 , pp. 16-26
    • Djakovitch, L.1    Heise, H.2    Kohler, K.3
  • 31
    • 33846893890 scopus 로고    scopus 로고
    • Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
    • DOI 10.1021/cr0505674
    • Yin, Y.; Liebscher, J. Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 2007, 107, 133-173. (Pubitemid 46223705)
    • (2007) Chemical Reviews , vol.107 , Issue.1 , pp. 133-173
    • Yin, L.1    Liebscher, J.2
  • 32
    • 0037061029 scopus 로고    scopus 로고
    • The leaching and re-deposition of metal species from and onto conventional supported palladium catalysts in the Heck reaction of iodobenzene and methyl acrylate in N-methylpyrrolidone
    • DOI 10.1016/S1381-1169(01)00436-8, PII S1381116901004368
    • Zhao, F.; Shirai, M.; Ikushima, Y.; Arai, M. The leaching and re-deposition of metal species from and onto conventional supported palladium catalysts in the Heck reaction of iodobenzene and methyl acrylate in N-methylpyrrolidone. J. Mol. Catal. A: Chem. 2002, 180, 211-219. (Pubitemid 34203958)
    • (2002) Journal of Molecular Catalysis A: Chemical , vol.180 , Issue.1-2 , pp. 211-219
    • Zhao, F.1    Shirai, M.2    Ikushima, Y.3    Arai, M.4
  • 33
    • 3142594439 scopus 로고    scopus 로고
    • Pd-catalyzed Heck arylation of cycloalkenes- studies on selectivity comparing homogeneous and heterogeneous catalysts
    • Wagner, M.; Hartung, G.G.; Beller, M.; Köhler, K. Pd-catalyzed Heck arylation of cycloalkenes- studies on selectivity comparing homogeneous and heterogeneous catalysts. J. Mol. Catal. A: Chem. 2004, 219, 121-130.
    • (2004) J. Mol. Catal. A: Chem. , vol.219 , pp. 121-130
    • Wagner, M.1    Hartung, G.G.2    Beller, M.3    Köhler, K.4
  • 34
    • 0001637540 scopus 로고    scopus 로고
    • Highly selective palladium - Catalyzed Heck reaction of aryl bromides with cycloalkenes
    • Hartung, G.; Koehler, K.; Beller, M. Highly selective palladium - catalyzed Heck reaction of aryl bromides with cycloalkenes. Org. Lett. 1999, 1, 709-711.
    • (1999) Org. Lett. , vol.1 , pp. 709-711
    • Hartung, G.1    Koehler, K.2    Beller, M.3
  • 35
    • 54249150361 scopus 로고    scopus 로고
    • New trans-chelating ligands and their complexes and catalytic properties in the mizoroki - Heck arylation of cyclohexene
    • Kaganovsky, L.; Cho, K.-B.; Gelman, D. New trans-chelating ligands and their complexes and catalytic properties in the Mizoroki - Heck arylation of cyclohexene. Organometallics 2008, 27, 5139-5145.
    • (2008) Organometallics , vol.27 , pp. 5139-5145
    • Kaganovsky, L.1    Cho, K.-B.2    Gelman, D.3
  • 36
    • 33646525172 scopus 로고    scopus 로고
    • Model intermolecular, asymmetric Heck reactions catalyzed by chiral pyridyloxazoline palladium(II) complexes
    • Dodd, D.W.; Toews, H.E.; Carneiro, F.D.S.; Jennings, M.C.; Jones, N.D. Model intermolecular, asymmetric Heck reactions catalyzed by chiral pyridyloxazoline palladium(II) complexes. Inorg. Chim. Acta 2006, 329, 2850-2858.
    • (2006) Inorg. Chim. Acta , vol.329 , pp. 2850-2858
    • Dodd, D.W.1    Toews, H.E.2    Carneiro, F.D.S.3    Jennings, M.C.4    Jones, N.D.5
  • 37
    • 0037415535 scopus 로고    scopus 로고
    • Heck reaction of aryl halides with linear or cyclic alkenes catalysed by a tetraphosphine/palladium catalyst
    • DOI 10.1016/S0040-4039(02)02788-0, PII S0040403902027880
    • Berthiol, F.; Doucet, H.; Santelli, M. Heck reaction of aryl halides with linear or cyclic alkenes catalysed by tetraphosphine/palladium catalyst. Tetrahedron Lett. 2003, 44, 1221-1225. (Pubitemid 36144140)
    • (2003) Tetrahedron Letters , vol.44 , Issue.6 , pp. 1221-1225
    • Berthiol, F.1    Doucet, H.2    Santelli, M.3
  • 38
    • 17444399684 scopus 로고    scopus 로고
    • 1'-Carbopalladated-4-ferrocenyl-1,3-oxazolines as catalysts for Heck reactions: Further evidence in support of the Pd(0)/Pd(II) mechanism
    • DOI 10.1016/j.jorganchem.2005.02.035, PII S0022328X05001622
    • Rosol, M.; Moyano, A. 1,-carbopalladated-4-ferrocenyl-1,3-oxazolines as catalysts for Heck reactions: Further evidence in support of the Pd(0)/Pd(II) mechanism. J. Organomet. Chem. 2005, 690, 2291-2296. (Pubitemid 40539177)
    • (2005) Journal of Organometallic Chemistry , vol.690 , Issue.9 , pp. 2291-2296
    • Rosol, M.1    Moyano, A.2
  • 39
    • 34548774476 scopus 로고    scopus 로고
    • Use of deuterium labelling studies to determine the stereochemical outcome of palladium migration during an asymmetric intermolecular Heck reaction
    • Wheatley, B.M.M.; Keay, B.A. Use of deuterium labelling studies to determine the stereochemical outcome of palladium migration during an asymmetric intermolecular Heck reaction. J. Org. Chem. 2007, 72, 7253-7259.
    • (2007) J. Org. Chem. , vol.72 , pp. 7253-7259
    • Wheatley, B.M.M.1    Keay, B.A.2
  • 40
    • 0033534340 scopus 로고    scopus 로고
    • Tailoring aqueous solvents for organic reactions: Heck coupling reactions in high temperature water
    • Gron, L.U.; Tinsley, A.S. Tailoring aqueous solvents for organic reactions: Heck coupling reactions in high temperature water. Tetrahedron Lett. 1999, 40, 227-230.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 227-230
    • Gron, L.U.1    Tinsley, A.S.2
  • 41
    • 38649104126 scopus 로고    scopus 로고
    • Palladium nanoparticles supported on alumina-based oxides as heterogeneous catalysts of the suzuki-miyaura reaction
    • Gniewek, A.; Ziółkowski, J.J.; Trzeciak, A.M.; Zawadzki, M.; Grabowska, H.; Wrzyszcz, J. Palladium nanoparticles supported on alumina-based oxides as heterogeneous catalysts of the Suzuki-Miyaura reaction. J. Catal. 2008, 254, 121-130.
    • (2008) J. Catal. , vol.254 , pp. 121-130
    • Gniewek, A.1    Ziółkowski, J.J.2    Trzeciak, A.M.3    Zawadzki, M.4    Grabowska, H.5    Wrzyszcz, J.6
  • 42
    • 77951844472 scopus 로고    scopus 로고
    • The Heck arylation of mono- And disubstituted olefins catalyzed by palladium supported on alumina-based oxides
    • 2010, submitted
    • Mieczyńska, E.; Pryjomska-Ray, I.; Trzeciak, A.M.; Grabowska, H.; Zawadzki, M. The Heck arylation of mono- and disubstituted olefins catalyzed by palladium supported on alumina-based oxides. New J. Chem. 2010, submitted.
    • New J. Chem.
    • Mieczyńska, E.1    Pryjomska-Ray, I.2    Trzeciak, A.M.3    Grabowska, H.4    Zawadzki, M.5
  • 44
    • 33645347922 scopus 로고    scopus 로고
    • A unifying mechanism for all high-temperature Heck reactions. the role of palladium colloids and anionic species
    • De Vries, J.G. A unifying mechanism for all high-temperature Heck reactions. The role of palladium colloids and anionic species. Dalton Trans. 2006, 421-429.
    • (2006) Dalton Trans. , pp. 421-429
    • De Vries, J.G.1
  • 47
    • 33644857817 scopus 로고    scopus 로고
    • Acid-base surface propertis of binary systems based on aluminum and zirconium oxides
    • Romanova, R.G.; Petrova, E.V. Acid-base surface propertis of binary systems based on aluminum and zirconium oxides. Kinet. Catal. 2006, 47, 138-147.
    • (2006) Kinet. Catal. , vol.47 , pp. 138-147
    • Romanova, R.G.1    Petrova, E.V.2


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