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Volumn 14, Issue 2, 2014, Pages 2012-2023

Review on palladium-containing perovskites: Synthesis, physico-chemical properties and applications in catalysis

Author keywords

Catalysts; Palladium Containing Perovskites; Properties; Synthesis

Indexed keywords

CALCIUM DERIVATIVE; NANOMATERIAL; OXIDE; PALLADIUM; PEROVSKITE; TITANIUM;

EID: 84894172067     PISSN: 15334880     EISSN: 15334899     Source Type: Journal    
DOI: 10.1166/jnn.2014.9013     Document Type: Review
Times cited : (10)

References (143)
  • 1
    • 38949179884 scopus 로고    scopus 로고
    • Electrical properties of layered perovskite-type palladium oxides
    • S. Ayukawa, M. Kato, T. Noji, and Y. Koikea, Electrical properties of layered perovskite-type palladium oxides. Mater. Sci. Eng. B 148, 65 (2008).
    • (2008) Mater. Sci. Eng. B , vol.148 , pp. 65
    • Ayukawa, S.1    Kato, M.2    Noji, T.3    Koikea, Y.4
  • 2
    • 58149144579 scopus 로고    scopus 로고
    • Synthesis, structural, magnetic and transport properties of layered perovskite-related titanates, niobates and tantalates of the type A(n)B(n)O(3n + 2), A'A(k - 10B(k)O(3k + 1) and A(m)B(m-1)O(3m)
    • F. Lichtenberg, A. Herrnberger, and K. Wiedenmann, Synthesis, structural, magnetic and transport properties of layered perovskite-related titanates, niobates and tantalates of the type A(n)B(n)O(3n + 2), A'A(k - 10B(k)O(3k + 1) and A(m)B(m-1)O(3m). Prog. Solid State Chem. 36, 253 (2008).
    • (2008) Prog. Solid State Chem. , vol.36 , pp. 253
    • Lichtenberg, F.1    Herrnberger, A.2    Wiedenmann, K.3
  • 3
    • 84871490291 scopus 로고    scopus 로고
    • Resistance degradation in donor-doped PZT ceramic stacks with Ag/Pd electrodes: I. Phenomenology of processes
    • L. Andrejs and J. Fleig, Resistance degradation in donor-doped PZT ceramic stacks with Ag/Pd electrodes: I. Phenomenology of processes. J. Eur. Ceram. Soc. 33, 779 (2013).
    • (2013) J. Eur. Ceram. Soc. , vol.33 , pp. 779
    • Andrejs, L.1    Fleig, J.2
  • 4
    • 44549086574 scopus 로고    scopus 로고
    • Diesel fuel reforming using catalytic membrane reactors
    • M. V. Mundschau, C. G. Burk, and D. A. Gribble, Jr, Diesel fuel reforming using catalytic membrane reactors. Catal. Today 136, 190 (2008).
    • (2008) Catal. Today , vol.136 , pp. 190
    • Mundschau, M.V.1    Burk, C.G.2    Gribble, Jr.D.A.3
  • 8
    • 77950278574 scopus 로고    scopus 로고
    • Strontium-doped perovskites rival platinum catalysts for treating NOx in simulated diesel exhaust
    • C. H. Kim, G. Qi, K. Dahlberg, and W. Li, Strontium-doped perovskites rival platinum catalysts for treating NOx in simulated diesel exhaust. Science 327, 1624 (2010).
    • (2010) Science , vol.327 , pp. 1624
    • Kim, C.H.1    Qi, G.2    Dahlberg, K.3    Li, W.4
  • 10
    • 56949096916 scopus 로고    scopus 로고
    • Synthesis and characterization of Ni-cermet/proton conducting thin film electrolyte symmetrical assemblies
    • A. Essoumhi, G. Taillades, M. Taillades-Jacquin, D. J. Jones, and J. Roziére, Synthesis and characterization of Ni-cermet/proton conducting thin film electrolyte symmetrical assemblies. Solid State Ionics 179, 2155 (2008).
    • (2008) Solid State Ionics , vol.179 , pp. 2155
    • Essoumhi, A.1    Taillades, G.2    Taillades-Jacquin, M.3    Jones, D.J.4    Roziére, J.5
  • 11
    • 71749095989 scopus 로고    scopus 로고
    • Perovskite-type mixed oxides as catalytic material for NO removal
    • J. Zhu and A. Thomas, Perovskite-type mixed oxides as catalytic material for NO removal. Appl. Catal. B-Environ. 92, 225 (2009).
    • (2009) Appl. Catal. B-Environ. , vol.92 , pp. 225
    • Zhu, J.1    Thomas, A.2
  • 14
    • 33746986031 scopus 로고    scopus 로고
    • Fe-based perovskites substituted by copper and palladium for NO+CO reaction
    • R. Zhang, H. Alamdari, and S. Kaliaguine, Fe-based perovskites substituted by copper and palladium for NO+CO reaction. J. Catal. 242, 241 (2006).
    • (2006) J. Catal. , vol.242 , pp. 241
    • Zhang, R.1    Alamdari, H.2    Kaliaguine, S.3
  • 16
    • 33748466901 scopus 로고    scopus 로고
    • -3 monolithic catalysts for the combustion of methane under fuel-rich conditions
    • -3 monolithic catalysts for the combustion of methane under fuel-rich conditions. Catal. Today 117, 454 (2006).
    • (2006) Catal. Today , vol.117 , pp. 454
    • Cimino, S.1    Landi, G.2    Lisi, L.3    Russo, G.4
  • 17
    • 84876252203 scopus 로고    scopus 로고
    • Photocatalytic decomposition of methyl orange over nanosized perovskite-type oxides under visible light irradiation
    • M. W. Ha, W. Y. Jung, K. T. Lim, M. S. Lee, and S. S. Hong, Photocatalytic decomposition of methyl orange over nanosized perovskite-type oxides under visible light irradiation. J. Nanosci. Nanotechnol. 13, 2330 (2013).
    • (2013) J. Nanosci. Nanotechnol. , vol.13 , pp. 2330
    • Ha, M.W.1    Jung, W.Y.2    Lim, K.T.3    Lee, M.S.4    Hong, S.S.5
  • 19
    • 0011717658 scopus 로고
    • Selective catalytic activity reduction of NOx with N-free reductants
    • M. Shelef, Selective catalytic activity reduction of NOx with N-free reductants. Chem. Rev. 95, 209 (1995).
    • (1995) Chem. Rev. , vol.95 , pp. 209
    • Shelef, M.1
  • 20
    • 0028768016 scopus 로고
    • Selective reduction of NO by hydrocarbons and oxygenated hydrocarbons over metal-oxides catalysts
    • H. Hamada, Selective reduction of NO by hydrocarbons and oxygenated hydrocarbons over metal-oxides catalysts. Catal. Today 22, 21 (1994).
    • (1994) Catal. Today , vol.22 , pp. 21
    • Hamada, H.1
  • 21
    • 0001370131 scopus 로고
    • Selective reduction of nitrogenoxides by hydrocarbons under lear-burn conditions using supported ptatinium-group metal-catalysts
    • R. Burch and P. J. Millington, Selective reduction of nitrogenoxides by hydrocarbons under Lear-Burn conditions using supported ptatinium-group metal-catalysts. Catal. Today 26, 185 (1995).
    • (1995) Catal. Today , vol.26 , pp. 185
    • Burch, R.1    Millington, P.J.2
  • 22
    • 84876245602 scopus 로고    scopus 로고
    • Influence of a surfactant and reducing agent on preparation of palladium
    • S. C. Kim, S. C. Jung, Y. K. Park, H. G. Ahn, and S. G. Seo, Influence of a surfactant and reducing agent on preparation of palladium. J. Nanosci. Nanotechnol. 13, 1961 (2013).
    • (2013) J. Nanosci. Nanotechnol. , vol.13 , pp. 1961
    • Kim, S.C.1    Jung, S.C.2    Park, Y.K.3    Ahn, H.G.4    Seo, S.G.5
  • 23
    • 33749515284 scopus 로고    scopus 로고
    • Recent advances in Pd/C-catalyzed coupling reactions
    • M. Seki, Recent advances in Pd/C-catalyzed coupling reactions. Synthesis 2975 (2006).
    • (2006) Synthesis , vol.2975
    • Seki, M.1
  • 25
    • 0034689553 scopus 로고    scopus 로고
    • Palladium-catalyzed homogeneous and heterogeneous Heck reactions in NMP and water-mixed solvents using organic, inorganic and mixed bases
    • F. Zhao, M. Shirai, and M. Arai, Palladium-catalyzed homogeneous and heterogeneous Heck reactions in NMP and water-mixed solvents using organic, inorganic and mixed bases. J. Mol. Catal. A: Chem. 154, 39 (2000).
    • (2000) J. Mol. Catal. A: Chem. , vol.154 , pp. 39
    • Zhao, F.1    Shirai, M.2    Arai, M.3
  • 27
    • 0032477347 scopus 로고    scopus 로고
    • Heterogeneous Heck catalysis with palladium-grafted molecular sieves
    • C. P. Mehnert, D. W. Weaver, and J. Y. Ying, Heterogeneous Heck catalysis with palladium-grafted molecular sieves. J. Am. Chem. Soc. 120, 12289 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 12289
    • Mehnert, C.P.1    Weaver, D.W.2    Ying, J.Y.3
  • 28
    • 0034832488 scopus 로고    scopus 로고
    • Heck reaction catalyzed by Pdmodified zeolites
    • L. Djakovitch and K. Koehler, Heck reaction catalyzed by Pdmodified zeolites. J. Am. Chem. Soc. 123, 5990 (2001).
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5990
    • Djakovitch, L.1    Koehler, K.2
  • 29
    • 0035029450 scopus 로고    scopus 로고
    • Metallic palladium in the Heck reaction: Active catalyst or convenient precursor?
    • A. Biffis, M. Zecca, and M. Basato, Metallic palladium in the Heck reaction: Active catalyst or convenient precursor? Eur. J. Inorg. Chem. 1131 (2001).
    • (2001) Eur. J. Inorg. Chem. , vol.1131
    • Biffis, A.1    Zecca, M.2    Basato, M.3
  • 30
    • 0034253330 scopus 로고    scopus 로고
    • Heck reactions catalyzed by oxide-supported palladiumstructure- activity relationships
    • M. Wagner, K. Köhler, L. Djakovitch, S. Weinkauf, V. Hagen, and M. Muhler, Heck reactions catalyzed by oxide-supported palladiumstructure- activity relationships. Top. Catal. 13, 319 (2000).
    • (2000) Top. Catal. , vol.13 , pp. 319
    • Wagner, M.1    Köhler, K.2    Djakovitch, L.3    Weinkauf, S.4    Hagen, V.5    Muhler, M.6
  • 31
    • 0035866481 scopus 로고    scopus 로고
    • Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis
    • K. Köhler, M. Wagner, and L. Djakovitch, Supported palladium as catalyst for carbon-carbon bond construction (Heck reaction) in organic synthesis. Catal. Today 66, 105 (2001).
    • (2001) Catal. Today , vol.66 , pp. 105
    • Köhler, K.1    Wagner, M.2    Djakovitch, L.3
  • 32
    • 0002569103 scopus 로고    scopus 로고
    • Pd-Cu-exchanged montmorillonite K10 clay: An efficient and reusable heterogeneous catalyst for vinylation of aryl halides
    • R. K. Ramchandani, B. S. Uphade, M. P. Vinod, R. D. Wakharkar, V. R. Choudhary, and A. Sudalai, Pd-Cu-exchanged montmorillonite K10 clay: an efficient and reusable heterogeneous catalyst for vinylation of aryl halides. Chem. Commun. 2071 (1997).
    • (1997) Chem. Commun. , vol.2071
    • Ramchandani, R.K.1    Uphade, B.S.2    Vinod, M.P.3    Wakharkar, R.D.4    Choudhary, V.R.5    Sudalai, A.6
  • 33
    • 0033548447 scopus 로고    scopus 로고
    • Palladium chloride and tetraphenylphosphonium bromide intercalated clay as a new catalyst for the heck reaction
    • R. S. Varma, K. P. Naicker, and P. J. Liesen, Palladium chloride and tetraphenylphosphonium bromide intercalated clay as a new catalyst for the Heck reaction. Tetrahedron Lett. 40, 2075 (1999).
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2075
    • Varma, R.S.1    Naicker, K.P.2    Liesen, P.J.3
  • 34
    • 0000849514 scopus 로고    scopus 로고
    • The use of palladium on porous glass for catalytic coupling reactions
    • J. Li, A. W. H. Mau, and C. R. Strauss, The use of palladium on porous glass for catalytic coupling reactions. Chem. Commun. 1275 (1997).
    • (1997) Chem. Commun. , vol.1275
    • Li, J.1    Mau, A.W.H.2    Strauss, C.R.3
  • 36
    • 0035840198 scopus 로고    scopus 로고
    • Palladium metal catalysts in Heck C-C coupling reactions
    • A. Biffis, M. Zecca, and M. Basato, Palladium metal catalysts in Heck C-C coupling reactions. J. Mol. Catal. A: Chem. 173, 249 (2001).
    • (2001) J. Mol. Catal. A: Chem. , vol.173 , pp. 249
    • Biffis, A.1    Zecca, M.2    Basato, M.3
  • 40
    • 17844380034 scopus 로고    scopus 로고
    • Redox behavior of palladium at startup in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function
    • M. Uenishia, M. Taniguchi, H. Tanaka, M. Kimura, Y. Nishihata, J. Mizuki, and T. Kobayashie, Redox behavior of palladium at startup in the Perovskite-type LaFePdOx automotive catalysts showing a self-regenerative function. Appl. Catal. B-Environ. 57, 267 (2005).
    • (2005) Appl. Catal. B-Environ. , vol.57 , pp. 267
    • Uenishia, M.1    Taniguchi, M.2    Tanaka, H.3    Kimura, M.4    Nishihata, Y.5    Mizuki, J.6    Kobayashie, T.7
  • 45
    • 48049090695 scopus 로고    scopus 로고
    • 3-based catalysts for methane combustion
    • 3-based catalysts for methane combustion. Catal. Today 137, 318 (2008).
    • (2008) Catal. Today , vol.137 , pp. 318
    • Kucharczyk, B.1    Tylus, W.2
  • 47
    • 79955409892 scopus 로고    scopus 로고
    • Perovskite oxide nanowires: Syn thesis, property and structural characterization
    • X. Zhu, Z. Liu, and N. Ming, Perovskite oxide nanowires: synthesis, property and structural characterization. J. Nanosci. Nanotechol. 10, 4109 (2010).
    • (2010) J. Nanosci. Nanotechol. , vol.10 , pp. 4109
    • Zhu, X.1    Liu, Z.2    Ming, N.3
  • 56
    • 73649115997 scopus 로고    scopus 로고
    • Elucidation of structure-activity relationships of model three way catalysts for the combustion of methane
    • X. Wei, P. Hug, R. Figi, M. Trottmann, A. Weidenkaff, and D. Ferri, Elucidation of structure-activity relationships of model three way catalysts for the combustion of methane. Appl. Catal. B-Environ. 94, 27 (2010).
    • (2010) Appl. Catal. B-Environ. , vol.94 , pp. 27
    • Wei, X.1    Hug, P.2    Figi, R.3    Trottmann, M.4    Weidenkaff, A.5    Ferri, D.6
  • 59
    • 30144442157 scopus 로고    scopus 로고
    • Cuand Pd-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene
    • R. Zhang, A. Villanueva, H. Alamdari, and S. Kaliaguine, Cuand Pd-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene. J. Catal. 237, 368 (2006).
    • (2006) J. Catal. , vol.237 , pp. 368
    • Zhang, R.1    Villanueva, A.2    Alamdari, H.3    Kaliaguine, S.4
  • 64
    • 3142772702 scopus 로고    scopus 로고
    • 3 perovskites for catalytic combustion of methane
    • 3 perovskites for catalytic combustion of methane. Catal. Today 90, 121 (2004).
    • (2004) Catal. Today , vol.90 , pp. 121
    • Kucharczyk, B.1    Tylus, W.2
  • 66
    • 80052261515 scopus 로고    scopus 로고
    • Pd-integrated lanthanumtransition metal perovskites for methanol partial oxidation
    • C.-L. Li, C.-L. Wang, and Y.-C. Lin, Pd-integrated lanthanumtransition metal perovskites for methanol partial oxidation. Catal. Today 174, 135 (2011).
    • (2011) Catal. Today , vol.174 , pp. 135
    • Li, C.-L.1    Wang, C.-L.2    Lin, Y.-C.3
  • 68
    • 84862065162 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize
    • C. C. C. J. Seechurn, M. O. Kitching, T. J. Colacot, and V. Snieckus, Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize. Angew. Chem. Int. Ed. 51, 5062 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5062
    • Seechurn, C.C.C.J.1    Kitching, M.O.2    Colacot, T.J.3    Snieckus, V.4
  • 69
    • 84878638599 scopus 로고    scopus 로고
    • Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: A remarkable advance from palladium to nickel catalysts
    • F.-S. Han, Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: a remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 42, 5270 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 5270
    • Han, F.-S.1
  • 70
    • 0001758225 scopus 로고    scopus 로고
    • Theoretical studies in palladium and platinum molecular chemistry
    • A. Dedieu, Theoretical studies in palladium and platinum molecular chemistry. Chem. Rev. 100, 543 (2000).
    • (2000) Chem. Rev. , vol.100 , pp. 543
    • Dedieu, A.1
  • 71
    • 77349109953 scopus 로고    scopus 로고
    • Emergence of palladium (IV) chemistry in synthesis and catalysis
    • P. Sehnal, R. J. K. Taylor, and I. J. S. Fairlamb, Emergence of palladium (IV) chemistry in synthesis and catalysis. Chem. Rev. 110, 824 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 824
    • Sehnal, P.1    Taylor, R.J.K.2    Fairlamb, I.J.S.3
  • 72
    • 4043123499 scopus 로고    scopus 로고
    • Enantioselective palladiumcatalyzed transformations
    • L. F. Tietze, H. Ila, and H. P. Bell, Enantioselective palladiumcatalyzed transformations. Chem. Rev. 104, 3453 (2004).
    • (2004) Chem. Rev. , vol.104 , pp. 3453
    • Tietze, L.F.1    Ila, H.2    Bell, H.P.3
  • 73
    • 79954531716 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed alkene functionalization via nucleopalladation: Stereochemical pathways and enantioselective catalytic applications
    • R. I. McDonald, G. Liu, and S. S. Stahl, Palladium(II)-catalyzed alkene functionalization via nucleopalladation: Stereochemical pathways and enantioselective catalytic applications. Chem. Rev. 111, 2981 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 2981
    • McDonald, R.I.1    Liu, G.2    Stahl, S.S.3
  • 74
    • 84875818323 scopus 로고    scopus 로고
    • Enantioselective palladium-catalyzed decarboxylative allylation of carbazolones: Total synthesis of (-)-aspidospermidine and (+)-kopsihainanine A
    • Z. Q. Li, S. X. Zhang, S. T. Wu, X. L. Shen, L. W. Zou, F. Q. Wang, X. Li, F. Z. Peng, H. B. Zhang, and Z. H. Shao, Enantioselective palladium-catalyzed decarboxylative allylation of carbazolones: total synthesis of (-)-aspidospermidine and (+)-kopsihainanine A. Angw. Chem. Int. Ed. 52, 4117 (2013).
    • (2013) Angw. Chem. Int. Ed. , vol.52 , pp. 4117
    • Li, Z.Q.1    Zhang, S.X.2    Wu, S.T.3    Shen, X.L.4    Zou, L.W.5    Wang, F.Q.6    Li, X.7    Peng, F.Z.8    Zhang, H.B.9    Shao, Z.H.10
  • 75
    • 33846918696 scopus 로고    scopus 로고
    • Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
    • D. Alberico, M. E. Scott, and M. Lautens, Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem. Rev. 107, 174 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 174
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 76
    • 77349104061 scopus 로고    scopus 로고
    • Transition metal-catalyzed direct arylation of substrates with activated sp (3)-hybridized C H bonds and some of their synthetic equivalents with aryl halides and pseudohalides
    • F. Bellina and R. Rossi, Transition metal-catalyzed direct arylation of substrates with activated sp(3)-hybridized C H bonds and some of their synthetic equivalents with aryl halides and pseudohalides. Chem. Rev. 110, 1082 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 1082
    • Bellina, F.1    Rossi, R.2
  • 77
    • 33751424969 scopus 로고    scopus 로고
    • Synthesis of heterocycles via palladiumcatalyzed oxidative addition
    • G. Zeni and R. C. Larock, Synthesis of heterocycles via palladiumcatalyzed oxidative addition. Chem. Rev. 106, 4644 (2006).
    • (2006) Chem. Rev. , vol.106 , pp. 4644
    • Zeni, G.1    Larock, R.C.2
  • 78
    • 80054999158 scopus 로고    scopus 로고
    • Palladium-catalysed hydroxylation and alkoxylation
    • S. Enthaler and A. Company, Palladium-catalysed hydroxylation and alkoxylation. Chem. Soc. Rev. 40, 4912 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4912
    • Enthaler, S.1    Company, A.2
  • 79
    • 84872246718 scopus 로고    scopus 로고
    • Synthesis of heterocycles via palladium-catalyzed carbonylations
    • X.-F. Wu, H. Neumann, and M. Beller, Synthesis of heterocycles via palladium-catalyzed carbonylations. Chem. Rev. 113, 1 (2013).
    • (2013) Chem. Rev. , vol.113 , pp. 1
    • Wu, X.-F.1    Neumann, H.2    Beller, M.3
  • 80
    • 84866742794 scopus 로고    scopus 로고
    • Recent applications of the Suzuki reaction in total synthesis
    • M. M. Heravi and E. Hashemi, Recent applications of the Suzuki reaction in total synthesis. Tetraherdon, 68, 9145 (2012).
    • (2012) Tetraherdon , vol.68 , pp. 9145
    • Heravi, M.M.1    Hashemi, E.2
  • 81
    • 84877577341 scopus 로고    scopus 로고
    • Palladium-mediated total synthesis of bioactive natural products
    • K. C. Majumdar and B. Sinha, Palladium-mediated total synthesis of bioactive natural products. Synthesis 45, 1271 (2013).
    • (2013) Synthesis , vol.45 , pp. 1271
    • Majumdar, K.C.1    Sinha, B.2
  • 83
    • 0037944068 scopus 로고    scopus 로고
    • Palladium-assisted routes to nucleosides
    • L. A. Agrofoglio, I. Gillaizeau, and Y. Saito, Palladium-assisted routes to nucleosides. Chem. Rev. 103, 1875 (2003).
    • (2003) Chem. Rev. , vol.103 , pp. 1875
    • Agrofoglio, L.A.1    Gillaizeau, I.2    Saito, Y.3
  • 84
    • 84856937741 scopus 로고    scopus 로고
    • An efficient mixed-ligand Pd catalytic system to promote C-N coupling for the synthesis of N-arylaminotriazole nucleosides
    • Y. Fan, Y. Xia, J. Tang, F. Ziarelli, F. Qu, P. Rocchi, J. L. Iovanna, and L. Peng, An efficient mixed-ligand Pd catalytic system to promote C-N coupling for the synthesis of N-arylaminotriazole nucleosides. Chem. Eur. J. 18, 2221 (2012).
    • (2012) Chem. Eur. J. , vol.18 , pp. 2221
    • Fan, Y.1    Xia, Y.2    Tang, J.3    Ziarelli, F.4    Qu, F.5    Rocchi, P.6    Iovanna, J.L.7    Peng, L.8
  • 85
    • 80051754936 scopus 로고    scopus 로고
    • General and modular synthesis of isomeric 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides bearing diverse alkyl, aryl, hetaryl, amino, carbamoyl, and hydroxy groups
    • M. Štefko, L. Slavětínská B. Klepetářová and M. Hocek, General and modular synthesis of isomeric 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides bearing diverse alkyl, aryl, hetaryl, amino, carbamoyl, and hydroxy groups. J. Org. Chem. 76, 6619 (2011).
    • (2011) J. Org. Chem. , vol.76 , pp. 6619
    • Štefko, M.1    Slavětínská, L.2    Klepetá řová, B.3    Hocek, M.4
  • 86
    • 84875952816 scopus 로고    scopus 로고
    • Palladiumcatalyzed oxidative insertion of carbon monoxide to N-sulfonyl-2- aminobiaryls through C H bond activation: Access to bioactive phenanthridinone derivatives in one pot
    • V. Rajeshkumar, T. H. Lee, and S. C. Chuang, Palladiumcatalyzed oxidative insertion of carbon monoxide to N-sulfonyl-2- aminobiaryls through C H bond activation: Access to bioactive phenanthridinone derivatives in one pot. Org. Lett. 15, 1468 (2013).
    • (2013) Org. Lett. , vol.15 , pp. 1468
    • Rajeshkumar, V.1    Lee, T.H.2    Chuang, S.C.3
  • 89
    • 0142133661 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of novel erythrofuranosyl imidazo[1,2-A]pyridine C-nucleosides constructed via palladium coupling of iodoimidazo[12-A]pyridines and dihydrofuran
    • K. S. Gudmundsson, J. D. Williams, J. C. Drach, and L. B. Townsend, Synthesis and antiviral activity of novel erythrofuranosyl imidazo[1,2-A] pyridine C-nucleosides constructed via palladium coupling of iodoimidazo[1,2-A]pyridines and dihydrofuran. J. Med. Chem. 46, 1449 (2003).
    • (2003) J. Med. Chem. , vol.46 , pp. 1449
    • Gudmundsson, K.S.1    Williams, J.D.2    Drach, J.C.3    Townsend, L.B.4
  • 90
    • 80051736898 scopus 로고    scopus 로고
    • N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: A perfect union
    • G. C. Fortman and S. P. Nolan, N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union. Chem. Soc. Rev. 40, 5151 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 5151
    • Fortman, G.C.1    Nolan, S.P.2
  • 91
    • 84871993508 scopus 로고    scopus 로고
    • Homogeneous palladium-catalyzed asymmetric hydrogenation
    • Q.-A. Chen, Z.-S. Ye, Y. Duan, and Y.-G. Zhou, Homogeneous palladium-catalyzed asymmetric hydrogenation. Chem. Soc. Rev. 42, 497 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 497
    • Chen, Q.-A.1    Ye, Z.-S.2    Duan, Y.3    Zhou, Y.-G.4
  • 92
    • 65949122326 scopus 로고    scopus 로고
    • Application of the solvent water in twophase telomerisation reactions and recycling of the homogeneous palladium catalysts
    • A. Behr and J. Leschinski, Application of the solvent water in twophase telomerisation reactions and recycling of the homogeneous palladium catalysts. Green Chem. 11, 609 (2009).
    • (2009) Green Chem. , vol.11 , pp. 609
    • Behr, A.1    Leschinski, J.2
  • 94
    • 33846893890 scopus 로고    scopus 로고
    • Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
    • L. Yin and J. Liebscher, Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 107, 133 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 133
    • Yin, L.1    Liebscher, J.2
  • 95
    • 77954063984 scopus 로고    scopus 로고
    • Engineering metal organic frameworks for heterogeneous catalysis
    • A. Corma, H. Garcia, and F. X. Llabrés i Xamena, Engineering metal organic frameworks for heterogeneous catalysis. Chem. Rev. 110, 4606 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 4606
    • Corma, A.1    Garcia, H.2    Llabrés I Xamena, F.X.3
  • 96
    • 84877043533 scopus 로고    scopus 로고
    • Palladium nanoparticles supported on polymer: An efficient and reusable heterogeneous catalyst for the Suzuki cross-coupling reactions and aerobic oxidation of alcohols
    • K. Karami, M. Ghasemi, and N. H. Naeini, Palladium nanoparticles supported on polymer: An efficient and reusable heterogeneous catalyst for the Suzuki cross-coupling reactions and aerobic oxidation of alcohols. Catal. Comm. 38, 10 (2013).
    • (2013) Catal. Comm. , vol.38 , pp. 10
    • Karami, K.1    Ghasemi, M.2    Naeini, N.H.3
  • 97
    • 84879182649 scopus 로고    scopus 로고
    • Palladium nanoparticles supported on zif-8 as an efficient heterogeneous catalyst for aminocarbonylation
    • T. T. Dang, Y. H. Zhu, J. S. Y. Ngiam, S. C. Ghosh, A. Q. Chen, and A. M. Seayad, Palladium nanoparticles supported on ZIF-8 as an efficient heterogeneous catalyst for aminocarbonylation. ASC Catal. 3, 1406 (2013).
    • (2013) ASC Catal. , vol.3 , pp. 1406
    • Dang, T.T.1    Zhu, Y.H.2    Ngiam, J.S.Y.3    Ghosh, S.C.4    Chen, A.Q.5    Seayad, A.M.6
  • 98
    • 33947727055 scopus 로고    scopus 로고
    • The sonogashira reaction: A booming methodology in synthetic organic chemistry
    • R. Chinchilla and C. Nájera, The sonogashira reaction: A booming methodology in synthetic organic chemistry. Chem. Rev. 107, 922 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 922
    • Chinchilla, R.1    Nájera, C.2
  • 99
    • 80053319803 scopus 로고    scopus 로고
    • Copper-free Sonogashira cross-coupling for functionalization of alkyne-encoded proteins in aqueous medium and in bacterial cells
    • N. Li, R. K. V. Lim, S. Edwardraja, and Q. Lin, Copper-free Sonogashira cross-coupling for functionalization of alkyne-encoded proteins in aqueous medium and in bacterial cells. J. Am. Chem. Soc. 133, 15316 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15316
    • Li, N.1    Lim, R.K.V.2    Edwardraja, S.3    Lin, Q.4
  • 100
    • 84877123349 scopus 로고    scopus 로고
    • One-pot and regiospecific synthesis of 2,3-disubstituted indoles from 2-bromoanilides via consecutive palladium-catalyzed Sonogashira coupling, amidopalladation, and reductive elimination
    • B. Z. Lu, H. X. Wei, Y. D. Zhang, W. Y. Zhao, M. Dufour, G. S. Li, V. Farina, and C. H. Senanayake, One-pot and regiospecific synthesis of 2,3-disubstituted indoles from 2-bromoanilides via consecutive palladium-catalyzed Sonogashira coupling, amidopalladation, and reductive elimination. J. Org. Chem. 78, 4558 (2013).
    • (2013) J. Org. Chem. , vol.78 , pp. 4558
    • Lu, B.Z.1    Wei, H.X.2    Zhang, Y.D.3    Zhao, W.Y.4    Dufour, M.5    Li, G.S.6    Farina, V.7    Senanayake, C.H.8
  • 101
    • 0034249671 scopus 로고    scopus 로고
    • The heck reaction as a sharpening stone of palladium catalysis
    • I. P. Beletskaya and A. V. Cheprakov, The heck reaction as a sharpening stone of palladium catalysis. Chem. Rev. 100, 3009 (2000).
    • (2000) Chem. Rev. , vol.100 , pp. 3009
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 102
    • 0042379984 scopus 로고    scopus 로고
    • The asymmetric intramolecular Heck reaction in natural product total synthesis
    • A. B. Dounay and L. E. Overman, The asymmetric intramolecular Heck reaction in natural product total synthesis. Chem. Rev. 103, 2945 (2003).
    • (2003) Chem. Rev. , vol.103 , pp. 2945
    • Dounay, A.B.1    Overman, L.E.2
  • 103
    • 84880526269 scopus 로고    scopus 로고
    • Solar energy assisted starchstabilized palladium nanoparticles and their application in C-C coupling reactions
    • A. B. Patil and B. M. Bhanage, Solar energy assisted starchstabilized palladium nanoparticles and their application in C-C coupling reactions. J. Nanosci. Nanotechnol. 13, 5061 (2013).
    • (2013) J. Nanosci. Nanotechnol. , vol.13 , pp. 5061
    • Patil, A.B.1    Bhanage, B.M.2
  • 104
    • 79952677383 scopus 로고    scopus 로고
    • Intermolecular dehydrogenative Heck reactions
    • J. Le Bras and J. Muzart, Intermolecular dehydrogenative Heck reactions. Chem. Rev. 111, 1170 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 1170
    • Le Bras, J.1    Muzart, J.2
  • 105
    • 79952657415 scopus 로고    scopus 로고
    • Stille polycondensation for synthesis of functional materials
    • B. Carsten, F. He, H. J. Son, T. Xu, and L. Yu, Stille polycondensation for synthesis of functional materials. Chem. Rev. 111, 1493 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 1493
    • Carsten, B.1    He, F.2    Son, H.J.3    Xu, T.4    Yu, L.5
  • 106
    • 80054730816 scopus 로고    scopus 로고
    • Palladium nanoparticles immobilized on chemically modified silica gel: Efficient heterogeneous catalyst for Suzuki, Stille and Sonogashira cross-coupling reactions
    • P. Dutta and A. Sarkar, Palladium nanoparticles immobilized on chemically modified silica gel: Efficient heterogeneous catalyst for Suzuki, Stille and Sonogashira cross-coupling reactions. Adv. Synth. Catal. 353, 2814 (2011).
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 2814
    • Dutta, P.1    Sarkar, A.2
  • 107
    • 80051748635 scopus 로고    scopus 로고
    • Palladium-catalyzed alkynylation of secondary α-bromo carbonyl compounds via Stille coupling
    • J. Y. Kang and B. T. Connell, Palladium-catalyzed alkynylation of secondary α-bromo carbonyl compounds via Stille coupling. J. Org. Chem. 76, 6856 (2011).
    • (2011) J. Org. Chem. , vol.76 , pp. 6856
    • Kang, J.Y.1    Connell, B.T.2
  • 108
    • 57549099215 scopus 로고    scopus 로고
    • Palladium-catalyzed Suzuki- Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands
    • R. Martin and S. L. Buchwald, Palladium-catalyzed Suzuki- Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Acc. Chem. Res. 41, 1461 (2008).
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1461
    • Martin, R.1    Buchwald, S.L.2
  • 109
    • 34848907405 scopus 로고    scopus 로고
    • Synthesis of polysubstituted imidazo [1,2- a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation
    • J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, Synthesis of polysubstituted imidazo[1,2- a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation. J. Org. Chem. 72, 7650 (2007).
    • (2007) J. Org. Chem. , vol.72 , pp. 7650
    • Koubachi, J.1    El Kazzouli, S.2    Berteina-Raboin, S.3    Mouaddib, A.4    Guillaumet, G.5
  • 110
    • 23244451883 scopus 로고    scopus 로고
    • Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions
    • S. El Kazzouli, L. Bouissane, M. Khouili, and G. Guillaumet, Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions. Tetrahedron Lett. 46, 6163 (2005).
    • (2005) Tetrahedron Lett. , vol.46 , pp. 6163
    • El Kazzouli, S.1    Bouissane, L.2    Khouili, M.3    Guillaumet, G.4
  • 112
    • 84863011479 scopus 로고    scopus 로고
    • Microwave-assisted facile synthesis of palladium nanoparticles in HEPES solution and their size-dependent catalytic activities to Suzuki reaction
    • W. Zhang, Q. Wang, F. Qin, H. M. Zhou, Z. Lu, and R. Chen, Microwave-assisted facile synthesis of palladium nanoparticles in HEPES solution and their size-dependent catalytic activities to Suzuki reaction. J. Nanosci. Nanotechnol. 11, 7794 (2011).
    • (2011) J. Nanosci. Nanotechnol. , vol.11 , pp. 7794
    • Zhang, W.1    Wang, Q.2    Qin, F.3    Zhou, H.M.4    Lu, Z.5    Chen, R.6
  • 113
    • 69249123855 scopus 로고    scopus 로고
    • Nickel-catalysed Negishi cross-coupling reactions: Scope and mechanisms
    • V. B. Phapale and D. J. Cardenas, Nickel-catalysed Negishi cross-coupling reactions: Scope and mechanisms. Chem. Soc. Rev. 38, 1598 (2009).
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 1598
    • Phapale, V.B.1    Cardenas, D.J.2
  • 115
    • 34547943706 scopus 로고    scopus 로고
    • Investigations on the suzuki-miyaura and negishi couplings with alkenyl phosphates: Application to the synthesis of 1,1-disubstituted alkenes
    • A. L. Hansen, J. P. Ebran, T. M. Gogsig, and T. Skrydstrup, Investigations on the Suzuki-Miyaura and Negishi couplings with alkenyl phosphates: Application to the synthesis of 1,1-disubstituted alkenes. J. Org. Chem. 72, 6464 (2007).
    • (2007) J. Org. Chem. , vol.72 , pp. 6464
    • Hansen, A.L.1    Ebran, J.P.2    Gogsig, T.M.3    Skrydstrup, T.4
  • 116
    • 76249124052 scopus 로고    scopus 로고
    • Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resinsupported palladium complexes
    • Y. Hirai and Y. Uozumi, Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resinsupported palladium complexes. Chem. Comm. 46, 1103 (2010).
    • (2010) Chem. Comm. , vol.46 , pp. 1103
    • Hirai, Y.1    Uozumi, Y.2
  • 117
    • 84859970121 scopus 로고    scopus 로고
    • Ligand-free Buchwald-Hartwig aromatic aminations of aryl halides catalyzed by low-leaching and highly recyclable sulfur-modified gold-supported palladium
    • M. Al-Amin, T. Honma, N. Hoshiya, S. Shuto, and M. Arisawa, Ligand-free Buchwald-Hartwig aromatic aminations of aryl halides catalyzed by low-leaching and highly recyclable sulfur-modified gold-supported palladium. Adv. Synth. Catal. 354, 1061 (2012).
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 1061
    • Al-Amin, M.1    Honma, T.2    Hoshiya, N.3    Shuto, S.4    Arisawa, M.5
  • 118
    • 84866364612 scopus 로고    scopus 로고
    • Domino aziridine ring opening and Buchwald-Hartwig type coupling-cyclization by palladium catalyst
    • R. K. Rao, I. Karthikeyan, and G. Sekar, Domino aziridine ring opening and Buchwald-Hartwig type coupling-cyclization by palladium catalyst. Tetrahedron 68, 9090 (2012).
    • (2012) Tetrahedron , vol.68 , pp. 9090
    • Rao, R.K.1    Karthikeyan, I.2    Sekar, G.3
  • 119
    • 33845602612 scopus 로고    scopus 로고
    • Regioselective palladium-catalyzed arylation and heteroarylation of imidazo [1,2-A]pyridines
    • J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, Regioselective palladium-catalyzed arylation and heteroarylation of imidazo[1,2-A]pyridines. Synlett 3237 (2006).
    • (2006) Synlett , vol.3237
    • Koubachi, J.1    El Kazzouli, S.2    Berteina-Raboin, S.3    Mouaddib, A.4    Guillaumet, G.5
  • 121
    • 74849140182 scopus 로고    scopus 로고
    • Metal-catalyzed alphaarylation of carbonyl and related molecules: Novel trends in C C bond formation by C H bond functionalization
    • C. C. C. Johansson and T. J. Colacot, Metal-catalyzed alphaarylation of carbonyl and related molecules: Novel trends in C C bond formation by C H bond functionalization. Angw. Chem. Int. Ed. 49, 676 (2010).
    • (2010) Angw. Chem. Int. Ed. , vol.49 , pp. 676
    • Johansson, C.C.C.1    Colacot, T.J.2
  • 122
    • 80054972215 scopus 로고    scopus 로고
    • Transition metal-catalyzed arylation of unactivated C(sp(3)) H bonds
    • O. Baudoin, Transition metal-catalyzed arylation of unactivated C(sp(3)) H bonds. Chem. Soc. Rev. 40, 4902 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4902
    • Baudoin, O.1
  • 124
    • 78649612564 scopus 로고    scopus 로고
    • Transition-metalcatalyzed direct C-H alkenylation, alkynylation, benzylation, and alkylation of (hetero)arenes
    • S. Messaoudi, J. D. Brion, and M. Alami, Transition-metalcatalyzed direct C-H alkenylation, alkynylation, benzylation, and alkylation of (hetero)arenes. Eur. J. Org. Chem. 34, 6495 (2010).
    • (2010) Eur. J. Org. Chem. , vol.34 , pp. 6495
    • Messaoudi, S.1    Brion, J.D.2    Alami, M.3
  • 125
    • 84869403542 scopus 로고    scopus 로고
    • Free-amine-directed alkenylation of C(sp(2))-H and cycloamination by palladium catalysis
    • Z. J. Liang, L. Ju, Y. J. Xie, L. H. Huang, and Y. H. Zhang, Free-amine-directed alkenylation of C(sp(2))-H and cycloamination by palladium catalysis. Chem. Eur. J. 49, 15816 (2012).
    • (2012) Chem. Eur. J. , vol.49 , pp. 15816
    • Liang, Z.J.1    Ju, L.2    Xie, Y.J.3    Huang, L.H.4    Zhang, Y.H.5
  • 126
    • 50849118498 scopus 로고    scopus 로고
    • New and efficient palladium (0)-mediated microwave-assisted direct c3 alkenylation of imidazo[1,2-A]pyridines
    • J. Koubachi, S. El Kazzouli, S. Berteina-Raboin, A. Mouaddib, and G. Guillaumet, New and efficient palladium(0)-mediated microwave-assisted direct C3 alkenylation of imidazo[1,2- a]pyridines. Synthesis 2537 (2008).
    • (2008) Synthesis , vol.2537
    • Koubachi, J.1    El Kazzouli, S.2    Berteina-Raboin, S.3    Mouaddib, A.4    Guillaumet, G.5
  • 127
    • 84874025350 scopus 로고    scopus 로고
    • C2-selective direct alkynylation of indoles
    • G. L. Tolnai, S. Ganss, J. P. Brand, and J. Waser, C2-selective direct alkynylation of indoles. Org. Lett. 15, 112 (2013).
    • (2013) Org. Lett. , vol.15 , pp. 112
    • Tolnai, G.L.1    Ganss, S.2    Brand, J.P.3    Waser, J.4
  • 128
    • 84862572654 scopus 로고    scopus 로고
    • Palladium-catalyzed C H bond direct alkynylation of 5-membered heteroarenes: A well-defined synthetic route to azole derivatives containing two different alkynyl groups
    • F. Shibahara, Y. Dohke, and T. J. Murai, Palladium-catalyzed C H bond direct alkynylation of 5-membered heteroarenes: A well-defined synthetic route to azole derivatives containing two different alkynyl groups. J. Org. Chem. 77, 5381 (2013).
    • (2013) J. Org. Chem. , vol.77 , pp. 5381
    • Shibahara, F.1    Dohke, Y.2    Murai, T.J.3
  • 129
    • 0242694953 scopus 로고    scopus 로고
    • Palladium-containing perovskites: Recoverable and reuseable catalysts for Suzuki couplings
    • M. D. Smith, A. F. Stepan, C. Ramarao, P. E. Brennan, and S. V. Ley, Palladium-containing perovskites: Recoverable and reuseable catalysts for Suzuki couplings. Chem. Comm. 2652 (2003).
    • (2003) Chem. Comm. , vol.2652
    • Smith, M.D.1    Stepan, A.F.2    Ramarao, C.3    Brennan, P.E.4    Ley, S.V.5
  • 130
    • 18244366860 scopus 로고    scopus 로고
    • Heterogeneous or homogeneous? A case study involving palladiumcontaining perovskites in the Suzuki reaction
    • S. P. Andrews, A. F. Stepan, H. Tanaka, S. V. Ley, and M. D. Smith, Heterogeneous or homogeneous? A case study involving palladiumcontaining perovskites in the Suzuki reaction. Adv. Synth. Catal. 347, 647 (2005).
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 647
    • Andrews, S.P.1    Stepan, A.F.2    Tanaka, H.3    Ley, S.V.4    Smith, M.D.5
  • 131
    • 35348969025 scopus 로고    scopus 로고
    • Palladium-doped mixed oxides as 'slow-release' catalysts for Suzuki couplings
    • U. Kazmaier, S. Hähn, T. D. Weiss, R. Kautenburger, and W. F. Maier, Palladium-doped mixed oxides as 'slow-release' catalysts for Suzuki couplings. Synlett. 16, 2579 (2007).
    • (2007) Synlett. , vol.16 , pp. 2579
    • Kazmaier, U.1    Hähn, S.2    Weiss, T.D.3    Kautenburger, R.4    Maier, W.F.5
  • 132
    • 84878638599 scopus 로고    scopus 로고
    • Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: A remarkable advance from palladium to nickel catalysts
    • F.-S. Han, Transition-metal-catalyzed Suzuki-Miyaura crosscoupling reactions: a remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 42, 5270 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 5270
    • Han, F.-S.1
  • 133
    • 84872563127 scopus 로고    scopus 로고
    • Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations
    • S. L. Zultanski and G. C. Fu, Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations. J. Am. Chem. Soc. 135, 624 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 624
    • Zultanski, S.L.1    Fu, G.C.2
  • 134
    • 84865643904 scopus 로고    scopus 로고
    • Multifunctional mesoporous silica supported palladium nanoparticles as efficient and reusable catalyst for water-medium Ullmann reaction
    • J. L. Huang, J. W. Yin, W. Chai, C. Liang, J. Shen, and F. Zhang, Multifunctional mesoporous silica supported palladium nanoparticles as efficient and reusable catalyst for water-medium Ullmann reaction. New J. Chem. 36, 1378 (2012).
    • (2012) New J. Chem. , vol.36 , pp. 1378
    • Huang, J.L.1    Yin, J.W.2    Chai, W.3    Liang, C.4    Shen, J.5    Zhang, F.6
  • 135
    • 79951933560 scopus 로고    scopus 로고
    • New role of graphene oxide as active hydrogen donor in the recyclable palladium nanoparticles catalyzed ullmann reaction in environmental friendly ionic liquid/supercritical carbon dioxide system
    • J. S. Cheng, G. C. Zhang, J. H. Du, L. Y. Tang, J. Y. Xu, and J. H. Li, New role of graphene oxide as active hydrogen donor in the recyclable palladium nanoparticles catalyzed ullmann reaction in environmental friendly ionic liquid/supercritical carbon dioxide system. J. Mat. Chem. 21, 3485 (2011).
    • (2011) J. Mat. Chem. , vol.21 , pp. 3485
    • Cheng, J.S.1    Zhang, G.C.2    Du, J.H.3    Tang, L.Y.4    Xu, J.Y.5    Li, J.H.6
  • 137
    • 0242459935 scopus 로고    scopus 로고
    • First examples of transition-metal free Sonogashira-type couplings
    • N. E. Leadbeater, M. Marco, and B. J. Tominack, First examples of transition-metal free Sonogashira-type couplings. Org. Lett. 5, 3919 (2003).
    • (2003) Org. Lett. , vol.5 , pp. 3919
    • Leadbeater, N.E.1    Marco, M.2    Tominack, B.J.3
  • 138
    • 2342583283 scopus 로고    scopus 로고
    • Palladium-free and ligand-free Sonogashira cross-coupling
    • M. B. Thathagar, J. Beckers, and G. Rothenberg, Palladium-free and ligand-free Sonogashira cross-coupling. Green Chem. 6, 215 (2004).
    • (2004) Green Chem. , vol.6 , pp. 215
    • Thathagar, M.B.1    Beckers, J.2    Rothenberg, G.3
  • 139
    • 0347992908 scopus 로고    scopus 로고
    • Transitionmetal- free Sonogashira-type coupling reactions in water
    • P. Appukkuttan, W. Dehaen, and E. Van der Eycken, Transitionmetal- free Sonogashira-type coupling reactions in water. Eur. J. Org. Chem. 4713 (2003).
    • (2003) Eur. J. Org. Chem. , vol.4713
    • Appukkuttan, P.1    Dehaen, W.2    Eycken Der E.Van3
  • 140
    • 80054995660 scopus 로고    scopus 로고
    • 35 years of palladium-catalyzed cross-coupling with Grignard reagents: How far have we come?
    • C. E. I. Knappke and A. J. von Wangelin, and J. von Wangelin, 35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come? Chem. Soc. Rev. 40, 4948 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4948
    • Knappke, C.E.I.1    Von Wangelin, A.J.2    Von Wangelin, J.3
  • 141
    • 84870879744 scopus 로고    scopus 로고
    • Palladiumcatalyzed Kumada coupling reaction of bromoporphyrins with silylmethyl Grignard reagents: Preparation of silylmethyl-substituted porphyrins as a multipurpose synthon for fabrication of porphyrin systems
    • N. Sugita, S. Hayashi, F. Hino, and T. Takanami, Palladiumcatalyzed Kumada coupling reaction of bromoporphyrins with silylmethyl Grignard reagents: Preparation of silylmethyl-substituted porphyrins as a multipurpose synthon for fabrication of porphyrin systems. J. Org. Chem. 77, 10488 (2012).
    • (2012) J. Org. Chem. , vol.77 , pp. 10488
    • Sugita, N.1    Hayashi, S.2    Hino, F.3    Takanami, T.4
  • 142
    • 74849133511 scopus 로고    scopus 로고
    • DHTP Ligands for the highly ortho-selective, palladium-catalyzed cross-coupling of dihaloarenes with Grignard reagents: A Conformational Approach for Catalyst Improvement
    • S. Ishikawa and K. Manabe, DHTP Ligands for the highly ortho-selective, palladium-catalyzed cross-coupling of dihaloarenes with Grignard reagents: A Conformational Approach for Catalyst Improvement. Angew. Chem. Int. Ed. 49, 779 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 779
    • Ishikawa, S.1    Manabe, K.2
  • 143
    • 78651386712 scopus 로고    scopus 로고
    • Cross-coupling of Grignard reagents with alkyl halides or tosylates by the use of nickel or palladium containing perovskite
    • S. P. Singh, T. Iwasaki, J. Terao, and N. Kambe, Cross-coupling of Grignard reagents with alkyl halides or tosylates by the use of nickel or palladium containing perovskite. Tetrahedron Lett. 52, 774 (2011).
    • (2011) Tetrahedron Lett. , vol.52 , pp. 774
    • Singh, S.P.1    Iwasaki, T.2    Terao, J.3    Kambe, N.4


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