![Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X1300867X-fx1.jpg)
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - 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](https://pubs.rsc.org/image/article/2017/RA/c6ra25816f/c6ra25816f-s8_hi-res.gif)
New protocols to access imidazoles and their ring fused analogues: synthesis from N -propargylamines - RSC Advances (RSC Publishing) DOI:10.1039/C6RA25816F
![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](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
![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](https://pubs.rsc.org/image/article/2015/OB/c5ob01505g/c5ob01505g-s4_hi-res.gif)
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](http://www.scielo.br/img/revistas/jbchs/v25n12//0103-5053-jbchs-25-12-2186-gf32.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![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](https://www.researchgate.net/publication/336598288/figure/fig2/AS:864356392767491@1583090031981/The-palladium-imidazole-complexes-I-V-used-in-these-studies_Q320.jpg)
PDF) Efficient hydroarylation of terminal alkynes with sodium tetraphenylborate performed in water under mild conditions
![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](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/c1417aa0-7aa0-406c-b59b-6e22c58f3b0f/mfig000.jpg)
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
![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](https://www.scielo.br/img/revistas/jbchs/v30n10//0103-5053-jbchs-30-10-2114-gf02.jpg)
Are Imidazoles Versatile or Promiscuous in Reactions with Organophosphates? Insights from the Case of Parathion
![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](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
![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](https://ars.els-cdn.com/content/image/1-s2.0-S1566736719303516-t1.jpg)
Imidazole-aryl coupling reaction via CH bond activation catalyzed by palladium supported on modified magnetic reduced graphene oxide in alkaline deep eutectic solvent - 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 platinum(II) and palladium(II) quinoline-imine-pyridine, quinoline-imine-thiazole and quinoline-imine-imidazole complexes by metal-assisted condensation reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X11002476-fx1.jpg)
New platinum(II) and palladium(II) quinoline-imine-pyridine, quinoline-imine-thiazole and quinoline-imine-imidazole complexes by metal-assisted condensation reactions - ScienceDirect
![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](https://onlinelibrary.wiley.com/cms/asset/4d2b7199-cf7a-449d-8a5a-bdb03754a0cb/adsc201901189-toc-0001-m.jpg)
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
![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](http://www.scielo.br/img/revistas/jbchs/v25n12//0103-5053-jbchs-25-12-2186-gf09.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11243-017-0174-4/MediaObjects/11243_2017_174_Figa_HTML.gif)
A thiosemicarbazone–palladium(II)–imidazole complex as an efficient pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room temperature in aqueous media | 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](http://www.scielo.br/img/revistas/jbchs/v25n12//0103-5053-jbchs-25-12-2186-gf04.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![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](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-019-08414-8/MediaObjects/41467_2019_8414_Fig1_HTML.png)
Electrooxidative para -selective C–H/N–H cross-coupling with hydrogen evolution to synthesize triarylamine derivatives | Nature Communications
![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-019-02536-z/MediaObjects/10593_2019_2536_Figa_HTML.jpg)
The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink
![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](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
![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 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](https://pubs.rsc.org/image/article/2014/CC/c4cc07732f/c4cc07732f-s1_hi-res.gif)
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
![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](https://d3i71xaburhd42.cloudfront.net/fc55128389dcbec126d99bbd16b1822023ac6d80/4-Table1-1.png)