Palladium| BLD Pharm
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
Chelation assistance as a tool for the selective preparation of an imidazole-based mesoionic palladium carbene complex - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC07732F
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion
Table 1 from Interaction Between Pd(RaaiR/)Cl2 and HQ: Reaction Dynamics and Mechanism (RaaiR/ = 1-alkyl-2-(arylazo)imidazole; HQ = 8-Quinolinol) | Semantic Scholar
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect
Tetranuclear Palladium Complexes of Abnormal N‐Heterocyclic Carbene Ligands and their Catalytic Activities in Mizoroki‐Heck Coupling Reaction of Electron‐Rich Aryl Chlorides - Lee - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
PDF) Efficient hydroarylation of terminal alkynes with sodium tetraphenylborate performed in water under mild conditions
![Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones - Tetrahedron Lett. - X-MOL](https://xpic.x-mol.com/20190826%2F10.1016_j.tetlet.2019.151080.jpg "Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones - Tetrahedron Lett. - X-MOL")
Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones - Tetrahedron Lett. - X-MOL
![Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML](https://www.mdpi.com/molecules/molecules-22-00399/article_deploy/html/images/molecules-22-00399-sch021.png "Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML")
Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
3-Methylpyridine | (C5H4N)CH3 - PubChem
Regiocontrolled Synthesis of 1,2‐Diaryl‐1H‐imidazoles by Palladium‐ and Copper‐Mediated Direct Coupling of 1‐Aryl‐1H‐imidazoles with Aryl Halides under Ligandless Conditions - Bellina - 2006 - European Journal of Organic Chemistry - Wiley Online Library
Palladium‐Based Catalysts Supported by Unsymmetrical XYC–1 Type Pincer Ligands: C5 Arylation of Imidazoles and Synthesis of Octinoxate Utilizing the Mizoroki–Heck Reaction - Eur. J. Inorg. Chem. - X-MOL
Palladium‐ and Copper‐Mediated Direct C‐2 Arylation of Azoles — Including Free (NH)‐Imidazole, ‐Benzimidazole and ‐Indole — Under Base‐Free and Ligandless Conditions - Bellina - 2006 - European Journal of Organic Chemistry - Wiley Online Library
![Synthesis, Structural Characterization, and Coordination Chemistry of (Trineopentylphosphine)palladium(aryl)bromide Dimer Complexes ([(Np3P)Pd(Ar)Br]2) - Inorg. Chem. - X-MOL](https://xpic.x-mol.com/20190926%2F10.1021_acs.inorgchem.9b02164.jpg "Synthesis, Structural Characterization, and Coordination Chemistry of (Trineopentylphosphine)palladium(aryl)bromide Dimer Complexes ([(Np3P)Pd(Ar)Br]2) - Inorg. Chem. - X-MOL")
Synthesis, Structural Characterization, and Coordination Chemistry of (Trineopentylphosphine)palladium(aryl)bromide Dimer Complexes ([(Np3P)Pd(Ar)Br]2) - Inorg. Chem. - X-MOL
Imidazole-aryl coupling reaction via CH bond activation catalyzed by palladium supported on modified magnetic reduced graphene oxide in alkaline deep eutectic solvent - ScienceDirect
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion
US20170240515A1 - A one pot process for synthesis of oxazoline and imidazole compounds from glycerol - Google Patents
![Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML](https://www.mdpi.com/molecules/molecules-22-00399/article_deploy/html/images/molecules-22-00399-sch013.png "Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML")
Molecules | Free Full-Text | Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives | HTML
New platinum(II) and palladium(II) quinoline-imine-pyridine, quinoline-imine-thiazole and quinoline-imine-imidazole complexes by metal-assisted condensation reactions - ScienceDirect
![Direct arylation and Suzuki-Miyaura coupling of imidazo[1,2-a]pyridines catalyzed by (SIPr)Pd(allyl)Cl complex under microwave-irradiation | El Abbouchi | Mediterranean Journal of Chemistry](http://medjchem.com/public/journals/1/cover_article_1124_en_US.png "Direct arylation and Suzuki-Miyaura coupling of imidazo[1,2-a]pyridines catalyzed by (SIPr)Pd(allyl)Cl complex under microwave-irradiation | El Abbouchi | Mediterranean Journal of Chemistry")