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vzhůru nohama šperky vejít se methyl pyridine imidazole palladium Ložiskový kruh Hlavní sídlo obrubník

Dimetallic Palladium‐NHC Complexes: Synthesis, Characterization, and  Catalytic Application for Direct C−H Arylation Reaction of Heteroaromatics  with Aryl Chlorides - Lee - 2020 - Advanced Synthesis & Catalysis -  Wiley Online Library
Dimetallic Palladium‐NHC Complexes: Synthesis, Characterization, and Catalytic Application for Direct C−H Arylation Reaction of Heteroaromatics with Aryl Chlorides - Lee - 2020 - Advanced Synthesis & Catalysis - 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

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

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

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

PDF) Efficient hydroarylation of terminal alkynes with sodium  tetraphenylborate performed in water under mild conditions
PDF) Efficient hydroarylation of terminal alkynes with sodium tetraphenylborate performed in water under mild conditions

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

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

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

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

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

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

Palladium‐Catalyzed C3 or C4 Direct Arylation of Heteroaromatic Compounds  with Aryl Halides by CH Bond Activation - Roger - 2010 - ChemCatChem -  Wiley Online Library
Palladium‐Catalyzed C3 or C4 Direct Arylation of Heteroaromatic Compounds with Aryl Halides by CH Bond Activation - Roger - 2010 - ChemCatChem - 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

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

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

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

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

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
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