Efficient, Selective, and Recyclable Palladium Catalysts in Carbon−Carbon Coupling Reactions

Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

Miyaura, N., & Suzuki, A. (1995) · Chemical Reviews · doi:10.1021/cr00039a007 · Cited by 12,817

A new family of mesoporous molecular sieves prepared with liquid crystal templates

Beck, J. S., Vartuli, J. C., Roth, W. J., Leonowicz, M. E., Kresge, C. T., Schmitt, K. D., Chu, C. T. W., Olson, D. H., Sheppard, E. W., McCullen, S. B., et al. (1992) · Journal of the American Chemical Society · doi:10.1021/ja00053a020 · Cited by 10,967

Nonionic Triblock and Star Diblock Copolymer and Oligomeric Surfactant Syntheses of Highly Ordered, Hydrothermally Stable, Mesoporous Silica Structures

Zhao, D., Huo, Q., Feng, J., Chmelka, B. F., & Stucky, G. D. (1998) · Journal of the American Chemical Society · doi:10.1021/ja974025i · Cited by 6,697

A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines

Sonogashira, K., Tohda, Y., & Hagihara, N. (1975) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)91094-3 · Cited by 5,208

The Heck Reaction as a Sharpening Stone of Palladium Catalysis

Beletskaya, I. P., & Cheprakov, A. V. (2000) · Chemical Reviews · doi:10.1021/cr9903048 · Cited by 3,902

Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction

Hassan, J., Sévignon, M., Gozzi, C., Schulz, E., & Lemaire, M. (2002) · Chemical Reviews · doi:10.1021/cr000664r · Cited by 3,663

Asymmetric Transition Metal-Catalyzed Allylic Alkylations

Trost, B. M., & Vranken, D. L. V. (1996) · Chemical Reviews · doi:10.1021/cr9409804 · Cited by 3,205

Nanoparticles as Recyclable Catalysts: The Frontier between Homogeneous and Heterogeneous Catalysis

Astruc, D., Lu, F., & Aranzaes, J. R. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200500766 · Cited by 3,131

The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry

Chinchilla, R., & Nájera, C. (2007) · Chemical Reviews · doi:10.1021/cr050992x · Cited by 2,974

Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998

Suzuki, A. (1999) · Journal of Organometallic Chemistry · doi:10.1016/s0022-328x(98)01055-9 · Cited by 2,916

Palladium‐Catalyzed Cross‐Coupling Reactions in Total Synthesis

Nicolaou, K. C., Bulger, P. G., & Sarlah, D. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200500368 · Cited by 2,708

Palladium-Catalyzed Coupling Reactions of Aryl Chlorides

Littke, A. F., & Fu, G. C. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-u · Cited by 2,700

Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update

Li, C.-J. (2005) · Chemical Reviews · doi:10.1021/cr030009u · Cited by 2,244

Carbon−Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts

Yin, & Liebscher, J. (2007) · Chemical Reviews · doi:10.1021/cr0505674 · Cited by 2,085

On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review

Phan, N. T. S., Van Der Sluys, M., & Jones, C. W. (2006) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200505473 · Cited by 1,905

Ionic liquids and catalysis: Recent progress from knowledge to applications

Olivier-Bourbigou, H., Magna, L., & Morvan, D. (2010) · Applied Catalysis A: General · doi:10.1016/j.apcata.2009.10.008 · Cited by 1,639

Magnetically Separable Nanocatalysts: Bridges between Homogeneous and Heterogeneous Catalysis

Shylesh, S., Schünemann, V., & Thiel, W. R. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905684 · Cited by 1,428

Fabrication of Hollow Palladium Spheres and Their Successful Application to the Recyclable Heterogeneous Catalyst for Suzuki Coupling Reactions

Kim, S.-W., Kim, M., Lee, W. Y., & Hyeon, T. (2002) · Journal of the American Chemical Society · doi:10.1021/ja026032z · Cited by 1,377

Palladium Reagents and Catalysts: New Perspectives for the 21st Century

Tsuji, J. (2004) · Wiley eBooks · doi:10.1002/0470021209 · Cited by 1,322

Design and Preparation of Organic−Inorganic Hybrid Catalysts

Wight, A. P., & Davis, M. E. (2002) · Chemical Reviews · doi:10.1021/cr010334m · Cited by 1,265

A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions

Widegren, J. A., & Finke, R. G. (2003) · Journal of Molecular Catalysis A: Chemical · doi:10.1016/s1381-1169(02)00728-8 · Cited by 1,245

Fabrication of Titania Nanofibers by Electrospinning

Li, D., & Xia, Y. (2003) · Nano Letters · doi:10.1021/nl034039o · Cited by 1,239

Organotrifluoroborates: Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction

Molander, G. A., & Ellis, N. (2007) · Accounts of Chemical Research · doi:10.1021/ar050199q · Cited by 935

Beiträge zur Kenntniss des Acetenylbenzols

Glaser, C. (1869) · Berichte der deutschen chemischen Gesellschaft · doi:10.1002/cber.186900201183 · Cited by 865

Palladium‐Based Catalytic Systems for the Synthesis of Conjugated Enynes by Sonogashira Reactions and Related Alkynylations

Doucet, H., & Hierso, J. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200602761 · Cited by 854

Palladium Nanoparticles as Efficient Green Homogeneous and Heterogeneous Carbon−Carbon Coupling Precatalysts: A Unifying View

Astruc, D. (2007) · Inorganic Chemistry · doi:10.1021/ic062183h · Cited by 779

Comprehensive Organic Name Reactions and Reagents

Wang, Z. (2010) · Wiley eBooks · doi:10.1002/9780470638859 · Cited by 769

Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji–Trost Reactions

Lamblin, M., Nassar‐Hardy, L., Hierso, J., Fouquet, É., & Felpin, F. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200900765 · Cited by 649

Ligand-free Heck reactions using low Pd-loading

Reetz, M. T., & de Vries, J. G. (2004) · Chemical Communications · doi:10.1039/b406719n · Cited by 644

A unifying mechanism for all high-temperature Heck reactions. The role of palladium colloids and anionic species

de Vries, J. G. (2006) · Dalton Trans. · doi:10.1039/b506276b · Cited by 624

Formation of Carbon−Carbon Bonds under Catalysis by Transition-Metal Nanoparticles

Moreno-Mañas, M., & Pleixats, R. (2003) · Accounts of Chemical Research · doi:10.1021/ar020267y · Cited by 612

Advances in the Heck chemistry of aryl bromides and chlorides

Whitcombe, N. J., Hii, K. K. (., & Gibson, S. E. (2001) · Tetrahedron · doi:10.1016/s0040-4020(01)00665-2 · Cited by 588

Homeopathic Ligand-Free Palladium as a Catalyst in the Heck Reaction. A Comparison with a Palladacycle

de Vries, A. H. M., Mulders, J. M. C. A., Mommers, J. H. M., Henderickx, H. J. W., & de Vries, J. G. (2003) · Organic Letters · doi:10.1021/ol035184b · Cited by 551

Silica-supported palladium: Sustainable catalysts for cross-coupling reactions

Polshettiwar, V., Len, C., & Fihri, A. (2009) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2009.06.001 · Cited by 512

Variations on a theme—recent developments on the mechanism of the Heck reaction and their implications for synthesis

T. Crisp, G. (1998) · Chemical Society Reviews · doi:10.1039/a827427z · Cited by 503

Continuous Flow Techniques in Organic Synthesis

Jas, G., & Kirschning, A. (2003) · Chemistry – A European Journal · doi:10.1002/chem.200305212 · Cited by 466

Palladium Nanoparticles Supported on Polyaniline Nanofibers as a Semi‐Heterogeneous Catalyst in Water

Gallon, B. J., Kojima, R. W., Kaner, R. B., & Diaconescu, P. L. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200701389 · Cited by 441

Palladium metal catalysts in Heck CC coupling reactions

Biffis, A., Zecca, M., & Basato, M. (2001) · Journal of Molecular Catalysis A Chemical · doi:10.1016/s1381-1169(01)00153-4 · Cited by 417

A Reassessment of the Transition-Metal Free Suzuki-Type Coupling Methodology

Arvela, R. K., Leadbeater, N. E., Sangi, M. S., Williams, V. A., Granados, P., & Singer, R. D. (2005) · The Journal of Organic Chemistry · doi:10.1021/jo048531j · Cited by 384

Nitrile-Functionalized Pyridinium Ionic Liquids: Synthesis, Characterization, and Their Application in Carbon−Carbon Coupling Reactions

Zhao, D., Fei, Z., Geldbach, T. J., Scopelliti, R., & Dyson, P. J. (2004) · Journal of the American Chemical Society · doi:10.1021/ja0463482 · Cited by 377

The Heck reaction in the production of fine chemicals

de Vries, J. G. (2001) · Canadian Journal of Chemistry · doi:10.1139/cjc-79-5-6-1086 · Cited by 356

Recent Advances in Functionalization of Mesoporous Silica

Vinu, A., Hossain, K. Z., & Ariga, K. (2005) · Journal of Nanoscience and Nanotechnology · doi:10.1166/jnn.2005.089 · Cited by 354

Ordered Mesoporous Pd/Silica−Carbon as a Highly Active Heterogeneous Catalyst for Coupling Reaction of Chlorobenzene in Aqueous Media

Wan, Y., Wang, H., Zhao, Q., Klingstedt, M., Terasaki, O., & Zhao, D. (2009) · Journal of the American Chemical Society · doi:10.1021/ja808481g · Cited by 351

A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides

Jin, M., & Lee, D. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905626 · Cited by 323

Heck Reactions of Iodobenzene and Methyl Acrylate with Conventional Supported Palladium Catalysts in the Presence of Organic and/or Inorganic Bases without Ligands

Zhao, F., Bhanage, B. M., Shirai, M., & Arai, M. (2000) · Chemistry - A European Journal · doi:10.1002/(sici)1521-3765(20000303)6:5<843::aid-chem843>3.0.co;2-g · Cited by 290

Pd/C: An Old Catalyst for New Applications – Its Use for the Suzuki–Miyaura Reaction

Felpin, F., Ayad, T., & Mitra, S. (2006) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200501004 · Cited by 284

Recyclable Palladium Catalyst for Highly Selective α Alkylation of Ketones with Alcohols

Kwon, M. S., Kim, N., Seo, S. H., Park, I. S., Cheedrala, R. K., & Park, J. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200502422 · Cited by 259

Toward green catalytic synthesis—Transition metal-catalyzed reactions in non-conventional media

Liu, S., & Xiao, J. (2007) · Journal of Molecular Catalysis A: Chemical · doi:10.1016/j.molcata.2007.01.003 · Cited by 255

Pd/C as a Reusable Catalyst for the Coupling Reaction of Halophenols and Arylboronic Acids in Aqueous Media

Sakurai, H., Tsukuda, T., & Hirao, T. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo016342k · Cited by 249

Heterogeneous Pd/C‐Catalyzed Ligand‐Free, Room‐Temperature Suzuki–Miyaura Coupling Reactions in Aqueous Media

Maegawa, T., Kitamura, Y., Sako, S., Udzu, T., Sakurai, A., Tanaka, A., Kobayashi, Y., Endo, K., Bora, U., Kurita, T., et al. (2007) · Chemistry – A European Journal · doi:10.1002/chem.200601795 · Cited by 241

Palladium Nanoparticles Captured in Microporous Polymers: A Tailor-Made Catalyst for Heterogeneous Carbon Cross-Coupling Reactions

Ogasawara, S., & Kato, S. (2010) · Journal of the American Chemical Society · doi:10.1021/ja9062053 · Cited by 205

Oxime Carbapalladacycle Covalently Anchored to High Surface Area Inorganic Supports or Polymers as Heterogeneous Green Catalysts for the Suzuki Reaction in Water

Baleizão, C., Corma, A., García, H., & Leyva, A. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo030302u · Cited by 205

Structural investigations of functionalized mesoporous silica-supported palladium catalyst for Heck and Suzuki coupling reactions

SHIMIZU, K., KOIZUMI, S., HATAMACHI, T., YOSHIDA, H., KOMAI, S., KODAMA, T., & KITAYAMA, Y. (2004) · Journal of Catalysis · doi:10.1016/j.jcat.2004.09.005 · Cited by 196

Immobilization of Pd(OAc)2 in Ionic Liquid on Silica: Application to Sustainable Mizoroki−Heck Reaction

Hagiwara, H., Sugawara, Y., Isobe, K., Hoshi, T., & Suzuki, T. (2004) · Organic Letters · doi:10.1021/ol049343i · Cited by 196

Nanoparticles and Catalysis

(2008) · Focus on Catalysts · doi:10.1016/s1351-4180(08)70340-4 · Cited by 192

Recent Advances in Pd/C-Catalyzed Coupling Reactions

Seki, M. (2006) · Synthesis · doi:10.1055/s-2006-950197 · Cited by 191

Stabilisation of Pd(0) on surface functionalised Fe3O4 nanoparticles: magnetically recoverable and stable recyclable catalyst for hydrogenation and Suzuki–Miyaura reactions

Amali, A. J., & Rana, R. K. (2009) · Green Chemistry · doi:10.1039/b916261p · Cited by 189

A highly active and reusable heterogeneous catalyst for the Suzuki reaction: synthesis of biaryls and polyaryls

Paul, S., & Clark, J. H. (2003) · Green Chemistry · doi:10.1039/b306097g · Cited by 179

Heck Reaction Catalyzed by Nanosized Palladium on Chitosan in Ionic Liquids

Calò, V., Nacci, A., Monopoli, A., Fornaro, A., Sabbatini, L., Cioffi, N., & Ditaranto, N. (2004) · Organometallics · doi:10.1021/om049586e · Cited by 178

Highly Active Thermomorphic Fluorous Palladacycle Catalyst Precursors for the Heck Reaction; Evidence for a Palladium Nanoparticle Pathway

Rocaboy, C., & Gladysz, J. A. (2002) · Organic Letters · doi:10.1021/ol025790r · Cited by 176

Supported Ultra Small Palladium on Magnetic Nanoparticles Used as Catalysts for Suzuki Cross‐Coupling and Heck Reactions

Yinghuai, Z., Peng, S. C., Emi, A., Zhenshun, S., Monalisa, & Kemp, R. A. (2007) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200700021 · Cited by 167

Synthesis of Noble Metal Nanoparticles Embedded in the Shell Layer of Core−Shell Poly(styrene-co-4-vinylpyridine) Micospheres and Their Application in Catalysis

Wen, F., Zhang, W., Wei, G., Wang, Y., Zhang, J., Zhang, M., & Shi, L. (2008) · Chemistry of Materials · doi:10.1021/cm703378c · Cited by 165

Palladium Nanoparticles Stabilized by an Ionic Polymer and Ionic Liquid: A Versatile System for C−C Cross-Coupling Reactions

Yang, X., Fei, Z., Zhao, D., Ang, W. H., Li, Y., & Dyson, P. J. (2008) · Inorganic Chemistry · doi:10.1021/ic702305t · Cited by 158

A novel Suzuki reaction system based on a supported palladium catalyst

Mubofu, E. B., Clark, J. H., & Macquarrie, D. J. (2001) · Green Chemistry · doi:10.1039/b009190l · Cited by 150

Supported palladium as catalyst for carbon–carbon bond construction (Heck reaction) in organic synthesis

Köhler, K., Wagner, M., & Djakovitch, L. (2001) · Catalysis Today · doi:10.1016/s0920-5861(00)00610-6 · Cited by 148

Hybrid materials: versatile matrices for supporting homogeneous catalysts

Zamboulis, A., Moitra, N., Moreau, J. J. E., Cattoën, X., & Man, M. W. C. (2010) · Journal of Materials Chemistry · doi:10.1039/c000334d · Cited by 143

Transition Metal-Catalyzed Carbon−Carbon Bond Formation Suzuki, Heck, and Sonogashira Reactions Using Microwave and Microtechnology

Singh, B. K., Kaval, N., Tomar, S., der Eycken, E. V. V., & Parmar, V. S. (2008) · Organic Process Research & Development · doi:10.1021/op800047f · Cited by 135

NC-palladacycles as highly effective cheap precursors for the phosphine-free Heck reactions

Beletskaya, I. P., Kashin, A. N., Karlstedt, N. B., Mitin, A. V., Cheprakov, A. V., & Kazankov, G. M. (2001) · Journal of Organometallic Chemistry · doi:10.1016/s0022-328x(00)00876-7 · Cited by 134

Review on green chemistry Suzuki cross coupling in aqueous media

Franzén, R. G., & Xu, Y. (2005) · Canadian Journal of Chemistry · doi:10.1139/v05-048 · Cited by 127

Polyethyleneglycol as scaffold and solvent for reusable C C coupling homogeneous Pd catalysts

Corma, A., Garcı́a, H., & Leyva‐Pérez, A. (2006) · Journal of Catalysis · doi:10.1016/j.jcat.2006.03.007 · Cited by 124

Palladium Nanoclusters Supported on Propylurea‐Modified Siliceous Mesocellular Foam for Coupling and Hydrogenation Reactions

Erathodiyil, N., Ooi, S., Seayad, A. M., Han, Y., Lee, S. S., & Ying, J. Y. (2008) · Chemistry - A European Journal · doi:10.1002/chem.200701361 · Cited by 121

Synthesis and characteristics of carbon encapsulated magnetic nanoparticles produced by a hydrothermal reaction

Wang, Z., Xiao, P., & He, N. (2006) · Carbon · doi:10.1016/j.carbon.2006.06.026 · Cited by 119

Continuous Microflow Synthesis of Butyl Cinnamate by a Mizoroki−Heck Reaction Using a Low-Viscosity Ionic Liquid as the Recycling Reaction Medium

Liu, S., Fukuyama, T., Sato, M., & Ryu, I. (2004) · Organic Process Research & Development · doi:10.1021/op034200h · Cited by 119

A Mild and Versatile Method for Palladium‐Catalyzed Cross‐Coupling of Aryl Halides in Water and Surfactants

Arcadi, A., Cerichelli, G., Chiarini, M., Correa, N. M., & Zorzan, D. H. (2003) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200300356 · Cited by 117

A Microcapillary System for Simultaneous, Parallel Microwave‐Assisted Synthesis

Comer, E., & Organ, M. G. (2005) · Chemistry - A European Journal · doi:10.1002/chem.200500820 · Cited by 112

Synthesis of Pd/Fe3O4 nanoparticle-based catalyst for the cross-coupling of acrylic acid with iodobenzene

Wang, Z., Shen, B. Q., Aihua, Z., & He, N. (2005) · Chemical Engineering Journal · doi:10.1016/j.cej.2005.08.003 · Cited by 111

The synthesis and applications of a micro-pine-structured nanocatalyst

Polshettiwar, V., Nadagouda, M. N., & Varma, R. S. (2008) · Chemical Communications · doi:10.1039/b814715a · Cited by 111

Monodisperse noble metal nanoparticles stabilized in SBA-15: Synthesis, characterization and application in microwave-assisted Suzuki–Miyaura coupling reaction

Zheng, Z., Li, H., Liu, T., & Cao, R. (2010) · Journal of Catalysis · doi:10.1016/j.jcat.2010.01.004 · Cited by 110

Chitosan-supported palladium(0) catalyst for microwave-prompted Suzuki cross-coupling reaction in water

Yi, S., Lee, D.-H., Sin, E., & Lee, Y. (2007) · Tetrahedron Letters · doi:10.1016/j.tetlet.2007.07.093 · Cited by 104

Hydroxyapatite-supported palladium (0) as a highly efficient catalyst for the Suzuki coupling and aerobic oxidation of benzyl alcohols in water

Jamwal, N., Gupta, M., & Paul, S. (2008) · Green Chemistry · doi:10.1039/b802135j · Cited by 99

Functionalization of electrospun ceramic nanofibre membranes with noble-metal nanostructures for catalytic applications

Formo, E. V., Yavuz, M. S., Lee, E. P., Lane, L. A., & Younan Xia, A. (2009) · Journal of Materials Chemistry · doi:10.1039/b901509d · Cited by 97

Palladium(0) Nanoparticles Stabilized by Phosphorus Dendrimers Containing Coordinating 15-Membered Triolefinic Macrocycles in Periphery

Badetti, E., Caminade, A., Majoral, J., Moreno‐Mañas, M., & Sebastián, R. M. (2008) · Langmuir · doi:10.1021/la7013418 · Cited by 90

Introduction to Cross-Coupling Reactions

Kohei, T., & Miyaura, N. (2002) · Topics in current chemistry · doi:10.1007/3-540-45313-x_1 · Cited by 87

Palladium-containing perovskites: recoverable and reuseable catalysts for Suzuki couplingsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b308465e/

Smith, M. D., Stepan, A. F., Ramarao, C., Brennan, P. E., & Ley, S. V. (2003) · Chemical Communications · doi:10.1039/b308465e · Cited by 85

Palladium Nanoparticles Supported on an Organic−Inorganic Fluorinated Hybrid Material. Application to Microwave-Based Heck Reaction

Niembro, S., Shafir, A., Vallribera, A., & Alibés, R. (2008) · Organic Letters · doi:10.1021/ol801091u · Cited by 78

Homogeneous Nanosize Palladium Catalysts

Tsuji, Y., & Fujihara, T. (2007) · Inorganic Chemistry · doi:10.1021/ic061872q · Cited by 76

Efficient Heck reactions catalyzed by a highly recyclable palladium(ii) complex of a pyridyl-functionalized imidazolium-based ionic liquid

Wang, R., Xiao, J., Twamley, B., & Shreeve, J. M. (2007) · Organic & Biomolecular Chemistry · doi:10.1039/b616529j · Cited by 75

Palladium on Activated Carbon - A Recyclable Catalyst for Suzuki-Miyaura Cross-Coupling of Aryl Chlorides in Water

Lysén, M., & Köhler, K. (2006) · Synthesis · doi:10.1055/s-2006-926305 · Cited by 71

Organotin Compounds

Fugami, K., & Kosugi, M. (2002) · Topics in current chemistry · doi:10.1007/3-540-45313-x_4 · Cited by 66

Nanosized metallic particles embedded in silica and carbon aerogels as catalysts in the Mizoroki–Heck coupling reaction

Martı́nez, S., Vallribera, A., Coteț, L. C., Popovici, M. I., Martín, L., Roig, A., Moreno‐Mañas, M., & Molins, E. (2005) · New Journal of Chemistry · doi:10.1039/b506784g · Cited by 63

Cobalt and Palladium Reagents in Organic Synthesis: The Beginning

Heck, R. F. (2006) · Synlett · doi:10.1055/s-2006-951536 · Cited by 62

An efficient and reusable catalyst based on Pd/CeO2 for the room temperature aerobic Suzuki–Miyaura reaction in water/ethanol

Amoroso, F., Colussi, S., Zotto, A. D., et al. (2009) · Journal of Molecular Catalysis A Chemical · doi:10.1016/j.molcata.2009.09.012 · Cited by 59

A Polymer-Supported Nickel(II) Catalyst for Room Temperature Tamao–Kumada–Corriu Coupling Reactions

Styring, P., Grindon, C., & Fisher, C. M. (2001) · Catalysis Letters · doi:10.1023/a:1013209202418 · Cited by 55

Hollow palladium–cobalt bimetallic nanospheres as an efficient and reusable catalyst for Sonogashira-type reactions

Li, H., Zhu, Z., Liu, J., Xie, S., & Li, H. (2010) · Journal of Materials Chemistry · doi:10.1039/b926347k · Cited by 40

Star-shaped heavily fluorinated aromatic sulfurs: stabilization of palladium nanoparticles active as catalysts in cross-coupling reactions

Niembro, S., Vallribera, A., & Moreno‐Mañas, M. (2007) · New Journal of Chemistry · doi:10.1039/b707776a · Cited by 33

Importance of the Conditioning of the Chitosan Support in a Catalyst‐Containing Ionic Liquid Phase Immobilised on Chitosan: The Palladium‐Catalysed Allylation Reaction Case

Moucel, R., Perrigaud, K., Goupil, J., Madec, P., Marinel, S., Guibal, E., Gaumont, A., & Dez, I. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200900515 · Cited by 32

Palladium supported on functionalized mesoporous silica as an efficient catalyst for Heck reaction

Wang, P., Lu, Q., & Li, J. (2009) · Materials Research Bulletin · doi:10.1016/j.materresbull.2009.09.034 · Cited by 31

On the Involvement of Palladium Nanoparticles in the Heck and Suzuki Reactions

Tsvelikhovsky, D., Popov, I., Gutkin, V., Rozin, A., Shvartsman, A., & Blum, J. (2008) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200800852 · Cited by 25

A Practical Synthesis of α,β-Unsaturated Imides, Useful Substrates For Asymmetric Conjugate Addition Reactions

Goodman, S. N., & Jacobsen, E. N. (2002) · Advanced Synthesis & Catalysis · doi:10.1002/1615-4169(200210)344:9<996::aid-adsc996>3.0.co;2-j · Cited by 22

Pd colloid grafted mesoporous silica and its extraordinarily high catalytic activity for Mizoroki–Heck reactions

Feng, Y., Li, L., Li, Y., Zhao, W., Gu, J., & Shi, J. (2010) · Journal of Molecular Catalysis A Chemical · doi:10.1016/j.molcata.2010.02.014 · Cited by 18

Konjac glucomannan supported palladium complex: An efficient and recyclable catalyst for Heck reaction

Liu, P., Yang, Y., Liu, Y., & Wang, X. (2007) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2007.07.031 · Cited by 8

Metal Catalysts for Heterogeneous Catalysis: From Single Atoms to Nanoclusters and Nanoparticles

Liu, L., & Corma, A. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00776 · Cited by 4,777

Nanocatalysts for Suzuki cross-coupling reactions

Fihri, A., Bouhrara, M., Nekoueishahraki, B., Basset, J.-M., & Polshettiwar, V. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15079k · Cited by 803

Which Metals are Green for Catalysis? Comparison of the Toxicities of Ni, Cu, Fe, Pd, Pt, Rh, and Au Salts

Egorova, K. S., & Ananikov, V. P. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201603777 · Cited by 490

Nanostructured Catalysts for Organic Transformations

Chng, L. L., Erathodiyil, N., & Ying, J. Y. (2013) · Accounts of Chemical Research · doi:10.1021/ar300197s · Cited by 450

Toward the Ideal Catalyst: From Atomic Centers to a “Cocktail” of Catalysts

Ananikov, V. P., & Beletskaya, I. P. (2012) · Organometallics · doi:10.1021/om201120n · Cited by 308