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Journal articles on the topic 'Palladium catalyzed C-C bond forming'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Liu, Yang, Zhongyi Mao, Alexandre Pradal, Pei-Qiang Huang, Julie Oble, and Giovanni Poli. "Palladium-Catalyzed [3 + 2]-C–C/N–C Bond-Forming Annulation." Organic Letters 20, no. 13 (2018): 4057–61. http://dx.doi.org/10.1021/acs.orglett.8b01616.

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2

Korwar, Sudha, Michael Burkholder, Stanley E. Gilliland, Kendra Brinkley, B. Frank Gupton, and Keith C. Ellis. "Chelation-directed C–H activation/C–C bond forming reactions catalyzed by Pd(ii) nanoparticles supported on multiwalled carbon nanotubes." Chemical Communications 53, no. 52 (2017): 7022–25. http://dx.doi.org/10.1039/c7cc02122d.

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3

Punia, Lavisha, Karu Ramesh, and Gedu Satyanarayana. "Palladium mediated domino reaction: synthesis of isochromenes under aqueous medium." RSC Advances 10, no. 1 (2020): 338–49. http://dx.doi.org/10.1039/c9ra08792c.

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4

Pilgrim, Ben S., Alice E. Gatland, Carlos H. A. Esteves, et al. "Palladium-catalyzed enolate arylation as a key C–C bond-forming reaction for the synthesis of isoquinolines." Organic & Biomolecular Chemistry 14, no. 3 (2016): 1065–90. http://dx.doi.org/10.1039/c5ob02320c.

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5

Kanchana, U. S., Elizabeth J. Diana, Thomas V. Mathew, and Gopinathan Anilkumar. "Palladium‐ Catalyzed C−P Bond Forming Reactions: An Overview." ChemistrySelect 6, no. 7 (2021): 1579–88. http://dx.doi.org/10.1002/slct.202004433.

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6

Rathin, Jana. "Synthesis of 1-Methoxyphenanthrene by Palladium-Catalyzed Heck Reaction." International Journal of HIT Transaction on ECCN Vol. 7, no. 2A (2021) (2021): 12–17. https://doi.org/10.5281/zenodo.5893120.

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Department of Chemistry, ShahidMatanginiHazra Govt. General Degree College for Women, Nimtouri, West Bengal A novel methodology for the synthesis of 1-methoxy phenanthrene has been developed via a palladium-assisted 6π electrocyclic reaction followed by formaldehyde elimination.

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7

Shaikh, Azam M., Bharat K. Sharma, Sajeev Chacko, and Rajesh M. Kamble. "Synthesis and opto-electrochemical properties of tribenzo[a,c,i]phenazine derivatives for hole transport materials." RSC Advances 6, no. 96 (2016): 94218–27. http://dx.doi.org/10.1039/c6ra20964e.

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In this work, five novel 3,6-disubstituted-tribenzo[a,c,i]phenazine (2–6) derivatives were synthesized in good yield by employing a palladium catalyzed C–N bond forming amination reaction and fully characterized.

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8

Cribbin, Liam, Brendan Twamley, Nicolae Buga, et al. "C–C Coupling in sterically demanding porphyrin environments." Beilstein Journal of Organic Chemistry 20 (November 4, 2024): 2784–98. http://dx.doi.org/10.3762/bjoc.20.234.

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Unlike their planar counterparts, classic synthetic protocols for C–C bond forming reactions on nonplanar porphyrins are underdeveloped. The development of C–C bond forming reactions on nonplanar porphyrins is critical in advancing this field of study for more complex porphyrin architectures, which could be used in supramolecular assemblies, catalysis, or sensing. In this work a library of arm-extended dodecasubstituted porphyrins was synthesized through the optimization of the classic Suzuki–Miyaura coupling of peripheral haloaryl substituents with a range of boronic acids. We report on palla

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9

Xie, Hujun, Ting Fan, Qunfang Lei, and Wenjun Fang. "New progress in theoretical studies on palladium-catalyzed C−C bond-forming reaction mechanisms." Science China Chemistry 59, no. 11 (2016): 1432–47. http://dx.doi.org/10.1007/s11426-016-0018-2.

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10

Shaikh, Azam M., Bharat K. Sharma, Sajeev Chacko, and Rajesh M. Kamble. "Synthesis and optoelectronic investigations of triarylamines based on naphtho[2,3-f]quinoxaline-7,12-dione core as donor–acceptors for n-type materials." RSC Advances 6, no. 65 (2016): 60084–93. http://dx.doi.org/10.1039/c6ra11149a.

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We have synthesized a new series of fully characterized donor–acceptor systems (2–7) involving electron donor triarylamines and electron acceptor naphtho[2,3-f]quinoxaline-7,12-dione by employing palladium catalyzed C–N bond forming amination reactions in good yields.

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11

Baranano, David, Grace Mann, and John F. Hartwig. "Nickel and Palladium-Catalyzed Cross-Couplings that Form Carbon-Heteroatom and Carbon-Element Bonds." Current Organic Chemistry 1, no. 3 (1997): 287–305. http://dx.doi.org/10.2174/1385272801666220124194647.

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The transition-metal catalyzed addition of heteroatom nucleophiles to aryl and vinyl halides is reviewed. This chemistry typically involves a nickel- or palladium-based catalyst containing phosphine ligands. In recently developed palladium-catalyzed chemistry, aryl halides react with amines in the presence of base to form arylamines. In similar chemistry catalyzed by both nickel and palladium, aryl and vinyl halides react with alkali metal or tin thiolates or selenides to form aryl and vinyl sulfides, while the reaction of different phosphorus compounds, such as phosphides, phosphonates, and

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12

Mori, Miwako, and Kazuyuki Doi. "Short Step Synthesis of 4-Substituted Indoles Using Palladium-catalyzed C-C Bond Forming Reaction." HETEROCYCLES 42, no. 1 (1996): 113. http://dx.doi.org/10.3987/com-95-s34.

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13

Dubbaka, Srinivas Reddy, and Pierre Vogel. "Palladium-catalyzed desulfinylative Negishi C–C bond forming cross-couplings of sulfonyl and organozinc chlorides." Tetrahedron Letters 47, no. 20 (2006): 3345–48. http://dx.doi.org/10.1016/j.tetlet.2006.03.101.

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14

Ho, Danny, Jonas Calleja та Matthew Gaunt. "Palladium(II)-Catalyzed C(sp3)–H Activation of N,O-Ketals towards a Method for the β-Functionalization of Ketones". Synlett 30, № 04 (2019): 454–58. http://dx.doi.org/10.1055/s-0037-1611664.

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A method for the formal β-functionalization of aliphatic ketones via a palladium-catalyzed sp3 C–H activation pathway is reported. An N,O-ketal directs an aliphatic C–H carbonylation to form γ-lactams which upon hydrolysis generate γ-keto carboxylic acids. This C–C bond-forming reaction is tolerant of a range of functional groups, enabling the synthesis of a range of synthetically important building blocks. Furthermore, the concepts underlying this transformation have also enabled the development of a related C–H alkenylation process to highly functionalised heterocycles.

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15

Kataoka, Noriyasu, Quinetta Shelby, James P. Stambuli, and John F. Hartwig. "Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings." Journal of Organic Chemistry 67, no. 16 (2002): 5553–66. http://dx.doi.org/10.1021/jo025732j.

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16

McErlain, Holly, Leanne M. Riley, and Andrew Sutherland. "Palladium-Catalyzed C–P Bond-Forming Reactions of Aryl Nonaflates Accelerated by Iodide." Journal of Organic Chemistry 86, no. 23 (2021): 17036–49. http://dx.doi.org/10.1021/acs.joc.1c02172.

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17

Palucki, Michael, John P. Wolfe, and Stephen L. Buchwald. "Synthesis of Oxygen Heterocycles via a Palladium-Catalyzed C−O Bond-Forming Reaction." Journal of the American Chemical Society 118, no. 42 (1996): 10333–34. http://dx.doi.org/10.1021/ja962408v.

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18

Tessema, Eskedar, Vijayanath Elakkat, Chiao-Fan Chiu, et al. "Recoverable Palladium-Catalyzed Carbon-Carbon Bond Forming Reactions under Thermomorphic Mode: Stille and Suzuki-Miyaura Reactions." Molecules 26, no. 5 (2021): 1414. http://dx.doi.org/10.3390/molecules26051414.

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The reaction of [PdCl2(CH3CN)2] and bis-4,4′-(RfCH2OCH2)-2,2′-bpy (1a–d), where Rf = n-C11F23 (a), n-C10F21 (b), n-C9F19 (c) and n-C8F17 (d), respectively, in the presence of dichloromethane (CH2Cl2) resulted in the synthesis of Pd complex, [PdCl2[4,4′-bis-(RfCH2OCH2)-2,2′-bpy] (2a–d). The Pd-catalyzed Stille arylations of vinyl tributyltin with aryl halides were selected to demonstrate the feasibility of recycling usage with 2a as the catalyst using NMP (N-methyl-2-pyrrolidone) as the solvent at 120–150 °C. Additionally, recycling and electronic effect studies of 2a–c were also carried out fo

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19

Pinto, Artur, Luc Neuville, Pascal Retailleau, and Jieping Zhu. "Synthesis of 3-(Diarylmethylenyl)oxindole by a Palladium-Catalyzed Domino Carbopalladation/C−H Activation/C−C Bond-Forming Process." Organic Letters 8, no. 21 (2006): 4927–30. http://dx.doi.org/10.1021/ol062022h.

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20

Naidu, Veluru Ramesh, and Jan-E. Bäckvall. "Synthesis of Cross-Conjugated Polyenes via Palladium-Catalyzed Oxidative C–C Bond Forming Cascade Reactions of Allenes." Journal of Organic Chemistry 85, no. 8 (2020): 5428–37. http://dx.doi.org/10.1021/acs.joc.0c00186.

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21

DOI, K., and M. MORI. "ChemInform Abstract: Short Step Synthesis of 4-Substituted Indoles Using Palladium- Catalyzed C-C Bond Forming Reaction." ChemInform 27, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199617100.

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22

Hirai, Yoshinori, and Yasuhiro Uozumi. "Preparation of Aryl(dicyclohexyl)phosphines by C–P Bond-Forming Cross-Coupling in Water Catalyzed by an Amphiphilic-Resin-Supported Palladium Complex." Synlett 28, no. 20 (2017): 2966–70. http://dx.doi.org/10.1055/s-0036-1590926.

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Aryl(dicyclohexyl)phosphines were prepared by a catalytic C–P bond-forming cross-coupling reaction of haloarenes with dicyclohexylphosphine under heterogeneous conditions in water containing an immobilized palladium complex coordinated to an amphiphilic polystyrene–poly(ethylene glycol) resin supported di(tert-butyl)phosphine ligand.

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23

Ramachandiran, Krishnan, Thonthula Sreelatha, Neelakandan Lakshmi, Thelagathoti Babu, Doraiswamy Muralidharan, and Paramasiram Perumal. "Palladium Catalyzed C–H Activation and its Application to Multi-bond Forming Reactions." Current Organic Chemistry 17, no. 18 (2013): 2001–24. http://dx.doi.org/10.2174/13852728113179990094.

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24

Lemen, Georgia S., and John P. Wolfe. "ChemInform Abstract: Palladium-Catalyzed Sp2 C-N Bond Forming Reactions: Recent Developments and Applications." ChemInform 46, no. 34 (2015): no. http://dx.doi.org/10.1002/chin.201534298.

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25

Chen, Li, Jiang-Bo Huang, Zheng Xu, et al. "Palladium-catalyzed Si–C bond-forming silylation of aryl iodides with hydrosilanes: an enhanced enantioselective synthesis of silicon-stereogenic silanes by desymmetrization." RSC Advances 6, no. 71 (2016): 67113–17. http://dx.doi.org/10.1039/c6ra12873d.

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An enantioselective Pd-catalyzed silicon–carbon bond-forming silylation reaction of aryl iodides with hydrosilanes for the synthesis of silicon-stereogenic silanes has been developed with good enantioselectivity under mild conditions.

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26

Mengue Me Ndong, Karen-Pacelye, Mina Hariri, Gabin Mwande-Maguene, et al. "Palladium-Catalyzed C-H Functionalization and Flame-Retardant Properties of Isophosphinolines." Molecules 29, no. 21 (2024): 5104. http://dx.doi.org/10.3390/molecules29215104.

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C-H activation is a powerful strategy for forming C-C bonds without the need for prefunctionalization. In this paper, we present a general, direct, and regioselective palladium-catalyzed functionalization of a phosphorus heterocycle, 2-phenyl-1H-isophosphinoline 2-oxide. The mild reaction conditions enabled the introduction of various functionalized alkenes. Moreover, the flame-retardant properties of selected products clearly highlighted the synergy between the phosphine oxide and another heteroatom-based group, even in the condensed phase.

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27

Ramachandiran, Krishnan, Thonthula Sreelatha, Neelakandan V. Lakshmi, Thelagathoti H. Babu, Doraiswamy Muralidharan, and Paramasiram T. Perumal. "ChemInform Abstract: Palladium Catalyzed C-H Activation and Its Application to Multi-Bond Forming Reactions." ChemInform 45, no. 42 (2014): no. http://dx.doi.org/10.1002/chin.201442286.

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28

PALUCKI, M., J. P. WOLFE, and S. L. BUCHWALD. "ChemInform Abstract: Synthesis of Oxygen Heterocycles via a Palladium-Catalyzed C-O Bond- Forming Reaction." ChemInform 28, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199707150.

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29

Ueda, Satoshi, Siraj Ali, Brett P. Fors, and Stephen L. Buchwald. "Me3(OMe)tBuXPhos: A Surrogate Ligand for Me4tBuXPhos in Palladium-Catalyzed C–N and C–O Bond-Forming Reactions." Journal of Organic Chemistry 77, no. 5 (2012): 2543–47. http://dx.doi.org/10.1021/jo202537e.

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30

Weber, Sven K., Sabrina Bremer, and Oliver Trapp. "Integration of reaction and separation in a micro-capillary column reactor—Palladium nanoparticle catalyzed C–C bond forming reactions." Chemical Engineering Science 65, no. 7 (2010): 2410–16. http://dx.doi.org/10.1016/j.ces.2009.09.006.

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31

Barboza, Amanda Aline, Juliana Arantes Dantas, Guilherme Augusto de Melo Jardim, Marco Antonio Barbosa Ferreira, Mateus Oliveira Costa, and Attilio Chiavegatti. "Recent Advances in Palladium-Catalyzed Oxidative Couplings in the Synthesis/Functionalization of Cyclic Scaffolds Using Molecular Oxygen as the Sole Oxidant." Synthesis 54, no. 09 (2021): 2081–102. http://dx.doi.org/10.1055/a-1701-7397.

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AbstractOver the past years, Pd(II)-catalyzed oxidative couplings have enabled the construction of molecular scaffolds with high structural diversity via C–C, C–N and C–O bond-forming reactions. In contrast to the use of stoichiometric amounts of more common oxidants, such as metal salts (Cu and Ag) and benzoquinone derivatives, the use of molecular oxygen for the direct or indirect regeneration of Pd(II) species presents itself as a more viable alternative in terms of economy and sustainability. In this review, we describe recent advances on the development of Pd-catalyzed oxidative cyclizati

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32

Pinto, Artur, Luc Neuville, and Jieping Zhu. "Palladium-Catalyzed Three-Component Synthesis of 3-(Diarylmethylene)oxindoles through a Domino Sonagashira/Carbopalladation/CH Activation/CC Bond-Forming Sequence." Angewandte Chemie 119, no. 18 (2007): 3355–59. http://dx.doi.org/10.1002/ange.200605192.

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33

Pinto, Artur, Luc Neuville, and Jieping Zhu. "Palladium-Catalyzed Three-Component Synthesis of 3-(Diarylmethylene)oxindoles through a Domino Sonagashira/Carbopalladation/CH Activation/CC Bond-Forming Sequence." Angewandte Chemie International Edition 46, no. 18 (2007): 3291–95. http://dx.doi.org/10.1002/anie.200605192.

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34

Abdulaeva, Inna A., Kirill P. Birin, Yulia G. Gorbunova, Aslan Yu Tsivadze, and Alla Bessmertnykh-Lemeune. "Post-synthetic methods for functionalization of imidazole-fused porphyrins." Journal of Porphyrins and Phthalocyanines 22, no. 08 (2018): 619–31. http://dx.doi.org/10.1142/s1088424618500475.

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Several methods for the post-synthetic modification of imidazo[4,5-[Formula: see text]]porphyrins are reported. First, a synthetic approach to the isomeric difunctionalized porphyrins, containing two [Formula: see text]-fused 2-aryl-1[Formula: see text]-imidazole cycles at adjacent or opposite pyrrole rings of the macrocycle is developed. The core chemistry of this synthetic route is the transformation of 2-aryl-1[Formula: see text]-imidazo[4,5-[Formula: see text]]porphyrins into corresponding imidazodioxochlorins followed by Debus–Radziszewski condensation with aromatic aldehyde. Next, 2-(4-b

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35

Ueda, Satoshi, Siraj Ali, Brett P. Fors, and Stephen L. Buchwald. "ChemInform Abstract: Me3(OMe)tBuXPhos: A Surrogate Ligand for Me4tBuXPhos in Palladium-Catalyzed C-N and C-O Bond-Forming Reactions." ChemInform 43, no. 27 (2012): no. http://dx.doi.org/10.1002/chin.201227035.

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36

Berrino, Roberta, Sandro Cacchi, Giancarlo Fabrizi, Antonella Goggiamani, and Paolo Stabile. "Arenediazonium tetrafluoroborates in palladium-catalyzed C–P bond-forming reactions. Synthesis of arylphosphonates, -phosphine oxides, and -phosphines." Organic & Biomolecular Chemistry 8, no. 20 (2010): 4518. http://dx.doi.org/10.1039/c0ob00243g.

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37

Bhilare, Shatrughn, Harshita Shet, Yogesh S. Sanghvi, and Anant R. Kapdi. "Discovery, Synthesis, and Scale-up of Efficient Palladium Catalysts Useful for the Modification of Nucleosides and Heteroarenes." Molecules 25, no. 7 (2020): 1645. http://dx.doi.org/10.3390/molecules25071645.

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Nucleic acid derivatives are imperative biomolecules and are involved in life governing processes. The chemical modification of nucleic acid is a fascinating area for researchers due to the potential activity exhibited as antiviral and antitumor agents. In addition, these molecules are also of interest toward conducting useful biochemical, pharmaceutical, and mutagenic study. For accessing such synthetically useful structures and features, transition-metal catalyzed processes have been proven over the years to be an excellent tool for carrying out the various transformations with ease and unde

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38

Yamada, Tsuyoshi, Jing Jiang, Naoya Ito, et al. "Development of Facile and Simple Processes for the Heterogeneous Pd-Catalyzed Ligand-Free Continuous-Flow Suzuki–Miyaura Coupling." Catalysts 10, no. 10 (2020): 1209. http://dx.doi.org/10.3390/catal10101209.

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The Suzuki–Miyaura coupling reaction is one of the most widely utilized C–C bond forming methods to create (hetero)biaryl scaffolds. The continuous-flow reaction using heterogeneous catalyst-packed cartridges is a practical and efficient synthetic method to replace batch-type reactions. A continuous-flow ligand-free Suzuki–Miyaura coupling reaction of (hetero)aryl iodides, bromides, and chlorides with (hetero)aryl boronic acids was developed using cartridges packed with spherical resin (tertiary amine-based chelate resin: WA30)-supported palladium catalysts (7% Pd/WA30). The void space in the

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39

Piou, Tiffany, Luc Neuville та Jieping Zhu. "Activation of a C(sp3)H Bond by a Transient σ-Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium-Catalyzed Domino Carbopalladation/C(sp3)C(sp3) Bond-Forming Process". Angewandte Chemie 124, № 46 (2012): 11729–33. http://dx.doi.org/10.1002/ange.201206267.

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40

Piou, Tiffany, Luc Neuville та Jieping Zhu. "Activation of a C(sp3)H Bond by a Transient σ-Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium-Catalyzed Domino Carbopalladation/C(sp3)C(sp3) Bond-Forming Process". Angewandte Chemie International Edition 51, № 46 (2012): 11561–65. http://dx.doi.org/10.1002/anie.201206267.

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41

Raduán, Mónica, Joaquim Padrosa, Anna Pla-Quintana, Teodor Parella, and Anna Roglans. "Functionalization of the 3-Position of Thiophene and Benzo[b]thiophene Moieties by Palladium-Catalyzed CC Bond Forming Reactions using Diazonium Salts." Advanced Synthesis & Catalysis 353, no. 11-12 (2011): 2003–12. http://dx.doi.org/10.1002/adsc.201100226.

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42

Abdul Khader, K. K., Ayyiliath M. Sajith, M. Syed Ali Padusha, H. P. Nagaswarupa, and A. Muralidharan. "ChemInform Abstract: Regioselective Synthesis of C-2 Substituted Imidazo[4,5-b]pyridines Utilizing Palladium Catalyzed C-N Bond Forming Reactions with Enolizable Heterocycles." ChemInform 45, no. 33 (2014): no. http://dx.doi.org/10.1002/chin.201433172.

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43

Iuliis, Marco Zimmer De, Iain DG Watson, Andrei K. Yudin, and Robert H. Morris. "A DFT investigation into the origin of regioselectivity in palladium-catalyzed allylic amination." Canadian Journal of Chemistry 87, no. 1 (2009): 54–62. http://dx.doi.org/10.1139/v08-078.

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The addition of amines or aziridines to prenylacetate is catalyzed by palladium phosphine complexes. The first-formed products have recently been shown to be the branched olefins R2NCMe2CH=CH2, R = alkyl, or R2 = 1,2-C6H10, for example. DFT calculations using the MPW1K functional were performed on reactions of the suspected intermediate η3-prenyl complex [Pd(η3-Me2CCHCH2)(PH3)2]+ with dimethylamine and ethylene imine. The activation barrier for the nucleophilic attack by the amine or the aziridine is calculated to be similar for either the sterically hindered site of the π-allyl ligand to prod

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44

Berrino, Roberta, Sandro Cacchi, Giancarlo Fabrizi, Antonella Goggiamani, and Paolo Stabile. "ChemInform Abstract: Arenediazonium Tetrafluoroborates in Palladium-Catalyzed C-P Bond-Forming Reactions. Synthesis of Arylphosphonates, -phosphine Oxides, and -phosphines." ChemInform 42, no. 7 (2011): no. http://dx.doi.org/10.1002/chin.201107202.

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45

Piou, Tiffany, Luc Neuville та Jieping Zhu. "ChemInform Abstract: Activation of a C(sp3)-H Bond by a Transient σ-Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium-Catalyzed Domino Carbopalladation/C(sp3)-C(sp3) Bond-Forming Process." ChemInform 44, № 14 (2013): no. http://dx.doi.org/10.1002/chin.201314130.

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46

Medvecký, Michal, Igor Linder, Luise Schefzig, Hans-Ulrich Reissig, and Reinhold Zimmer. "Iodination of carbohydrate-derived 1,2-oxazines to enantiopure 5-iodo-3,6-dihydro-2H-1,2-oxazines and subsequent palladium-catalyzed cross-coupling reactions." Beilstein Journal of Organic Chemistry 12 (December 29, 2016): 2898–905. http://dx.doi.org/10.3762/bjoc.12.289.

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Iodination of carbohydrate-derived 3,6-dihydro-2H-1,2-oxazines of type 3 using iodine and pyridine in DMF furnished 5-iodo-substituted 1,2-oxazine derivatives 4 with high efficacy. The alkenyl iodide moiety of 1,2-oxazine derivatives syn-4 and anti-4 was subsequently exploited for the introduction of new functionalities at the C-5 position by applying palladium-catalyzed carbon–carbon bond-forming reactions such as Sonogashira, Heck, or Suzuki coupling reactions as well as a cyanation reaction. These cross-coupling reactions led to a series of 5-alkynyl-, 5-alkenyl-, 5-aryl- and 5-cyano-substi

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47

Damian, Karen, Matthew L. Clarke, and Christopher J. Cobley. "Palladium‐catalysed P&bon;;C bond forming reactions between diphenylphosphine andortho‐substituted aryl bromides." Applied Organometallic Chemistry 23, no. 7 (2009): 272–76. http://dx.doi.org/10.1002/aoc.1510.

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48

Jung, Jong-Yeong, Jaewook Kim, and Hyunjoon Song. "2-Dimensional Palladium Organometallic Framework Generated Via C-H Activation for Electrochemical Syngas Production from CO₂." ECS Meeting Abstracts MA2024-02, no. 37 (2024): 2538. https://doi.org/10.1149/ma2024-02372538mtgabs.

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Noble metal catalysts have been recognized for their exceptional catalytic activity and efficiency, sparking extensive research efforts. Recently, there has been a notable shift towards utilizing noble metal catalysts supported on stable materials, particularly within the realm of heterogeneous catalysts. Metal-Organic Frameworks (MOFs) have emerged as promising candidates in this regard, offering versatile platforms that serve as porous substrates for dispersing external noble metal species. Various methodologies have been developed to fabricate MOF-based noble metal catalysts, including the

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Abdul Khader, K. K., Ayyiliath M. Sajith, M. Syed Ali Padusha, H. P. Nagaswarupa, and A. Muralidharan. "Regioselective synthesis of C-2 substituted imidazo[4,5-b]pyridines utilizing palladium catalysed C–N bond forming reactions with enolizable heterocycles." Tetrahedron Letters 55, no. 10 (2014): 1778–83. http://dx.doi.org/10.1016/j.tetlet.2014.01.114.

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Raduan, Monica, Joaquim Padrosa, Anna Pla-Quintana, Teodor Parella, and Anna Roglans. "ChemInform Abstract: Functionalization of the 3-Position of Thiophene and Benzo[b]thiophene Moieties by Palladium-Catalyzed C-C Bond Forming Reactions Using Diazonium Salts." ChemInform 43, no. 2 (2011): no. http://dx.doi.org/10.1002/chin.201202110.

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