307
61. Kishore R, Kantam ML, Yadav J, Sudhakar M, Laha S, Venugopal A (2013) Pd/Mg–La
mixed oxide catalyzed oxidative sp2 Csingle bondH bond acylation with alcohols. J. Mol.
Catal. A: Chem. 379:213
62. Kishore R, Yadav J, Venu B, Venugopal A, Kantam ML (2015) A Pd(ii)/Mg–La mixed oxide
catalyst for cyanation of aryl C–H bonds and tandem Suzuki–cyanation reactions. New
J. Chem. 39:5259
63. Fei H, Cohen SM (2015) Metalation of a Thiocatechol-Functionalized Zr(IV)-Based Metal–
Organic Framework for Selective C–H Functionalization. J. Am. Chem. Soc. 137:2191
64. Bai C, Yao X, Li Y (2015) Easy Access to Amides through Aldehydic C–H Bond
Functionalization Catalyzed by Heterogeneous Co-Based Catalysts. ACS Catal. 5:884
65. Pascanu V, Carson F, Solano MV, Su J, Zou X, Johansson MJ, Martín-Matute B (2016)
Selective Heterogeneous C−H Activation/Halogenation Reactions Catalyzed by Pd@MOF
Nanocomposites. Chem. – Eur. J. 22:3729
66. Chng LL, Zhang J, Yang J, Amoura M, Ying JY (2011) C–C Bond Formation via C–H
Activation and C–N Bond Formation via Oxidative Amination Catalyzed by Palladium‐
Polyoxometalate Nanomaterials Using Dioxygen as the Terminal Oxidant. Adv. Synth. Catal.
353:2988
67. Chen J, He L, Natte K, Neuman H, Beller M, Wu X-F (2014) Palladium@Cerium(IV) Oxide‐
Catalyzed Oxidative Synthesis of N‐(2‐Pyridyl)indoles via C–H Activation Reaction. Adv.
Synth. Catal. 356:2955
68. Zahmakiran M, Özkar S (2011) Metal nanoparticles in liquid phase catalysis; from recent
advances to future goals. Nanoscale 3:3462
69. Guo Z, Liu B, Zhang Q, Deng W, Wang Y, Yang Y (2014) Recent advances in heterogeneous
selective oxidation catalysis for sustainable chemistry. Chem. Soc. Rev. 43:3480
70. Bhaduri S, Mukesh D (2014) Homogeneous Catalysis: Mechanisms, Industrial Applications,
2nd Edition, Wiley
71. Blaser H-U (2003) Enantioselective catalysis in fine chemicals production. Chem
Commun: 293
72. Benaglia M (2009) Recoverable, Recyclable Catalysts; John Wiley & Sons: Chichester
73. Wittmann S, Schatz A, Grass R, Stark W, Reiser O (2010) A Recyclable Nanoparticle‐
Supported Palladium Catalyst for the Hydroxycarbonylation of Aryl Halides in Water.
Angew. Chem. Int. Ed. 49:1867
74. Basset J-M, Copéret C, Soulivong D, Taoufik M, Thivolle-Cazat (2010) Metathesis of
Alkanes and Related Reactions. J. Acc. Chem. Res. 43:323
75. Collis AEC, Horvath IT (2011) Heterogenization of homogeneous catalytic systems. Catal.
Sci. Technol. 1:912Collis AEC, Horvath IT (2011) Heterogenization of homogeneous catalytic systems. Catal. Sci. Technol. 1:912
76. Cole-Hamilton DJ (2003) Homogeneous Catalysis--New Approaches to Catalyst Separation,
Recovery, and Recycling. Science 299:1702
77. Carmichael AJ, Earle MJ, Holbrey JD, McCormac PB, Seddon KR (1999) The Heck Reaction
in Ionic Liquids: A Multiphasic Catalyst System. Org. Lett. 1:997
78. Pozzi G, Shepperson I (2003) Fluorous chiral ligands for novel catalytic systems. Coord
Chem Rev 242:115
79. Herrmann WA, Kohlpainter CW (1993) Water‐Soluble Ligands, Metal Complexes, and
Catalysts: Synergism of Homogeneous and Heterogeneous Catalysis. Angew Chem Int Ed
Engl 32:1524
80. De Vos DE, Vankelecom IFJ, Jacobs PA (eds) (2005) Chiral catalyst immobilization and
recycling. Wiley-VCH, Weinheim
81. Olmos A, Asensio G, Pérez PJ (2016) Homogeneous Metal-Based Catalysis in Supercritical
Carbon Dioxide as Reaction Medium. ACS Catal. 6:4265
82. Gava R, Olmos A, Noverges B, Varea T, Funes-Ardoiz I, Belderrain TR, Caballero A,
Maseras F, Asensio G, Pérez PJ (2015) Functionalization of CnH2n+2 Alkanes: Supercritical
Insights into Sustainable C–H Bond Activation
61. Kishore R, Kantam ML, Yadav J, Sudhakar M, Laha S, Venugopal A (2013) Pd/Mg–La
mixed oxide catalyzed oxidative sp2 Csingle bondH bond acylation with alcohols. J. Mol.
Catal. A: Chem. 379:213
62. Kishore R, Yadav J, Venu B, Venugopal A, Kantam ML (2015) A Pd(ii)/Mg–La mixed oxide
catalyst for cyanation of aryl C–H bonds and tandem Suzuki–cyanation reactions. New
J. Chem. 39:5259
63. Fei H, Cohen SM (2015) Metalation of a Thiocatechol-Functionalized Zr(IV)-Based Metal–
Organic Framework for Selective C–H Functionalization. J. Am. Chem. Soc. 137:2191
64. Bai C, Yao X, Li Y (2015) Easy Access to Amides through Aldehydic C–H Bond
Functionalization Catalyzed by Heterogeneous Co-Based Catalysts. ACS Catal. 5:884
65. Pascanu V, Carson F, Solano MV, Su J, Zou X, Johansson MJ, Martín-Matute B (2016)
Selective Heterogeneous C−H Activation/Halogenation Reactions Catalyzed by Pd@MOF
Nanocomposites. Chem. – Eur. J. 22:3729
66. Chng LL, Zhang J, Yang J, Amoura M, Ying JY (2011) C–C Bond Formation via C–H
Activation and C–N Bond Formation via Oxidative Amination Catalyzed by Palladium‐
Polyoxometalate Nanomaterials Using Dioxygen as the Terminal Oxidant. Adv. Synth. Catal.
353:2988
67. Chen J, He L, Natte K, Neuman H, Beller M, Wu X-F (2014) Palladium@Cerium(IV) Oxide‐
Catalyzed Oxidative Synthesis of N‐(2‐Pyridyl)indoles via C–H Activation Reaction. Adv.
Synth. Catal. 356:2955
68. Zahmakiran M, Özkar S (2011) Metal nanoparticles in liquid phase catalysis; from recent
advances to future goals. Nanoscale 3:3462
69. Guo Z, Liu B, Zhang Q, Deng W, Wang Y, Yang Y (2014) Recent advances in heterogeneous
selective oxidation catalysis for sustainable chemistry. Chem. Soc. Rev. 43:3480
70. Bhaduri S, Mukesh D (2014) Homogeneous Catalysis: Mechanisms, Industrial Applications,
2nd Edition, Wiley
71. Blaser H-U (2003) Enantioselective catalysis in fine chemicals production. Chem
Commun: 293
72. Benaglia M (2009) Recoverable, Recyclable Catalysts; John Wiley & Sons: Chichester
73. Wittmann S, Schatz A, Grass R, Stark W, Reiser O (2010) A Recyclable Nanoparticle‐
Supported Palladium Catalyst for the Hydroxycarbonylation of Aryl Halides in Water.
Angew. Chem. Int. Ed. 49:1867
74. Basset J-M, Copéret C, Soulivong D, Taoufik M, Thivolle-Cazat (2010) Metathesis of
Alkanes and Related Reactions. J. Acc. Chem. Res. 43:323
75. Collis AEC, Horvath IT (2011) Heterogenization of homogeneous catalytic systems. Catal.
Sci. Technol. 1:912Collis AEC, Horvath IT (2011) Heterogenization of homogeneous catalytic systems. Catal. Sci. Technol. 1:912
76. Cole-Hamilton DJ (2003) Homogeneous Catalysis--New Approaches to Catalyst Separation,
Recovery, and Recycling. Science 299:1702
77. Carmichael AJ, Earle MJ, Holbrey JD, McCormac PB, Seddon KR (1999) The Heck Reaction
in Ionic Liquids: A Multiphasic Catalyst System. Org. Lett. 1:997
78. Pozzi G, Shepperson I (2003) Fluorous chiral ligands for novel catalytic systems. Coord
Chem Rev 242:115
79. Herrmann WA, Kohlpainter CW (1993) Water‐Soluble Ligands, Metal Complexes, and
Catalysts: Synergism of Homogeneous and Heterogeneous Catalysis. Angew Chem Int Ed
Engl 32:1524
80. De Vos DE, Vankelecom IFJ, Jacobs PA (eds) (2005) Chiral catalyst immobilization and
recycling. Wiley-VCH, Weinheim
81. Olmos A, Asensio G, Pérez PJ (2016) Homogeneous Metal-Based Catalysis in Supercritical
Carbon Dioxide as Reaction Medium. ACS Catal. 6:4265
82. Gava R, Olmos A, Noverges B, Varea T, Funes-Ardoiz I, Belderrain TR, Caballero A,
Maseras F, Asensio G, Pérez PJ (2015) Functionalization of CnH2n+2 Alkanes: Supercritical
Insights into Sustainable C–H Bond Activation