The diimine ligand is coordinated to the palladium atom in a chelating,... | Download Scientific Diagram
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
![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
A thiosemicarbazone–palladium(II)–imidazole complex as an efficient pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room temperature in aqueous media | SpringerLink
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect
New protocols to access imidazoles and their ring fused analogues: synthesis from N -propargylamines - RSC Advances (RSC Publishing) DOI:10.1039/C6RA25816F
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - ScienceDirect
![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
Electrooxidative para -selective C–H/N–H cross-coupling with hydrogen evolution to synthesize triarylamine derivatives | Nature Communications
![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
US20110028733A1 - Process for the preparation of 5-(2-ethyl-dihydro-1h-inden-2-yl)-1h-imidazole and salts thereof - Google Patents
Palladium‐Catalyzed C3 or C4 Direct Arylation of Heteroaromatic Compounds with Aryl Halides by CH Bond Activation - Roger - 2010 - ChemCatChem - Wiley Online Library
US20170240515A1 - A one pot process for synthesis of oxazoline and imidazole compounds from glycerol - Google Patents
Palladium| BLD Pharm
![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")
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
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
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
3-Methylpyridine | (C5H4N)CH3 - PubChem
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
The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink
An optimized and versatile synthesis to pyridinylimidazole-type p38α mitogen activated protein kinase inhibitors - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01505G
Exploring Green Solvents Associated to Pd/C as Heterogeneous Catalyst for Direct Arylation of Heteroaromatics with Aryl Bromides - Mao - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
Molecular structure of C2. Selected bond distances (Å): Pd(1)−C(11)... | Download Scientific Diagram
