Home

Praktický Lechtání Kloktadlo methyl pyridine imidazole palladium Roucho morálka postupně

An optimized and versatile synthesis to pyridinylimidazole-type p38α  mitogen activated protein kinase inhibitors - Organic & Biomolecular  Chemistry (RSC Publishing) DOI:10.1039/C5OB01505G
An optimized and versatile synthesis to pyridinylimidazole-type p38α mitogen activated protein kinase inhibitors - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01505G

Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in  the Synthesis of Pharmaceutical Compounds
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

US20110028733A1 - Process for the preparation of  5-(2-ethyl-dihydro-1h-inden-2-yl)-1h-imidazole and salts thereof - Google  Patents
US20110028733A1 - Process for the preparation of 5-(2-ethyl-dihydro-1h-inden-2-yl)-1h-imidazole and salts thereof - Google Patents

Palladium–imidazole derivatives as highly active catalysts for Heck  reactions - ScienceDirect
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect

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‐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

Electrooxidative para -selective C–H/N–H cross-coupling with hydrogen  evolution to synthesize triarylamine derivatives | Nature Communications
Electrooxidative para -selective C–H/N–H cross-coupling with hydrogen evolution to synthesize triarylamine derivatives | Nature Communications

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
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

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

3-Methylpyridine | (C5H4N)CH3 - PubChem
3-Methylpyridine | (C5H4N)CH3 - PubChem

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
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

Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates?  Insights from the Case of Parathion
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion

The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling  of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink
The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink

Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in  the Synthesis of Pharmaceutical Compounds
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

Palladium| BLD Pharm
Palladium| BLD Pharm

A thiosemicarbazone–palladium(II)–imidazole complex as an efficient  pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room  temperature in aqueous media | SpringerLink
A thiosemicarbazone–palladium(II)–imidazole complex as an efficient pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room temperature in aqueous media | SpringerLink

US20170240515A1 - A one pot process for synthesis of oxazoline and imidazole  compounds from glycerol - Google Patents
US20170240515A1 - A one pot process for synthesis of oxazoline and imidazole compounds from glycerol - Google Patents

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
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

Imidazole-aryl coupling reaction via CH bond activation catalyzed by  palladium supported on modified magnetic reduced graphene oxide in alkaline  deep eutectic solvent - ScienceDirect
Imidazole-aryl coupling reaction via CH bond activation catalyzed by palladium supported on modified magnetic reduced graphene oxide in alkaline deep eutectic solvent - ScienceDirect

Molecular structure of C2. Selected bond distances (Å): Pd(1)−C(11)... |  Download Scientific Diagram
Molecular structure of C2. Selected bond distances (Å): Pd(1)−C(11)... | Download Scientific Diagram

The diimine ligand is coordinated to the palladium atom in a chelating,...  | Download Scientific Diagram
The diimine ligand is coordinated to the palladium atom in a chelating,... | Download Scientific Diagram

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

Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed  Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML

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
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

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
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

New platinum(II) and palladium(II) quinoline-imine-pyridine,  quinoline-imine-thiazole and quinoline-imine-imidazole complexes by  metal-assisted condensation reactions - ScienceDirect
New platinum(II) and palladium(II) quinoline-imine-pyridine, quinoline-imine-thiazole and quinoline-imine-imidazole complexes by metal-assisted condensation reactions - ScienceDirect

New protocols to access imidazoles and their ring fused analogues:  synthesis from N -propargylamines - RSC Advances (RSC Publishing)  DOI:10.1039/C6RA25816F
New protocols to access imidazoles and their ring fused analogues: synthesis from N -propargylamines - RSC Advances (RSC Publishing) DOI:10.1039/C6RA25816F

Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates?  Insights from the Case of Parathion
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion