![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-gf21.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions - Reaction Chemistry & Engineering (RSC Publishing) Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions - Reaction Chemistry & Engineering (RSC Publishing)](https://pubs.rsc.org/image/article/2019/re/c8re00235e/c8re00235e-s1_hi-res.gif)
Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions - Reaction Chemistry & Engineering (RSC Publishing)
DMSO-mediated palladium-catalyzed cyclization of two isothiocyanates via C–H sulfurization: a new route to 2-aminobenzothiazol
![Oxidative and Reductive Cross-Coupling Reactions Catalyzed by an Anionic “Ligandless” Palladium Complex - Org. Process Res. Dev. - X-MOL Oxidative and Reductive Cross-Coupling Reactions Catalyzed by an Anionic “Ligandless” Palladium Complex - Org. Process Res. Dev. - X-MOL](https://xpic.x-mol.com/20181206%2F10.1021_acs.oprd.8b00274.jpg)
Oxidative and Reductive Cross-Coupling Reactions Catalyzed by an Anionic “Ligandless” Palladium Complex - Org. Process Res. Dev. - X-MOL
![Figure 1 from On the mechanism of the palladium(II)-catalyzed decarboxylative olefination of arene carboxylic acids. Crystallographic characterization of non-phosphine palladium(II) intermediates and observation of their stepwise transformation in Heck ... Figure 1 from On the mechanism of the palladium(II)-catalyzed decarboxylative olefination of arene carboxylic acids. Crystallographic characterization of non-phosphine palladium(II) intermediates and observation of their stepwise transformation in Heck ...](https://d3i71xaburhd42.cloudfront.net/163ea142ccf3f831d1579f83352ecc45f7dcd733/2-Figure1-1.png)
Figure 1 from On the mechanism of the palladium(II)-catalyzed decarboxylative olefination of arene carboxylic acids. Crystallographic characterization of non-phosphine palladium(II) intermediates and observation of their stepwise transformation in Heck ...
![Table 1 from Palladium(II)-catalyzed oxidative dearomatization of free naphthols with two alkyne units. | Semantic Scholar Table 1 from Palladium(II)-catalyzed oxidative dearomatization of free naphthols with two alkyne units. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8417084044064b457c798a577f2b71c46a7d3170/2-Table1-1.png)
Table 1 from Palladium(II)-catalyzed oxidative dearomatization of free naphthols with two alkyne units. | Semantic Scholar
![Scheme 1 Synthesis of the chelating ligand 1 starting from commercially... | Download Scientific Diagram Scheme 1 Synthesis of the chelating ligand 1 starting from commercially... | Download Scientific Diagram](https://www.researchgate.net/profile/Christiane_Lang/publication/232273798/figure/fig6/AS:670548333969412@1536882589417/Scheme-1-Synthesis-of-the-chelating-ligand-1-starting-from-commercially-available.png)
Scheme 1 Synthesis of the chelating ligand 1 starting from commercially... | Download Scientific Diagram
DMSO-mediated palladium-catalyzed cyclization of two isothiocyanates via C–H sulfurization: a new route to 2-aminobenzothiazol
![Dimethyl Sulfoxide: Yesterday's Solvent, Today's Reagent - Tashrifi - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library Dimethyl Sulfoxide: Yesterday's Solvent, Today's Reagent - Tashrifi - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2eb219ed-efef-47aa-9f3d-fcf7f90942dc/adsc201901021-toc-0001-m.jpg)
Dimethyl Sulfoxide: Yesterday's Solvent, Today's Reagent - Tashrifi - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
![Synthesis and Catalytic Activity of Palladium Mediated Metallodendrimer for the Sonogashira and Heck Coupling Reactions Synthesis and Catalytic Activity of Palladium Mediated Metallodendrimer for the Sonogashira and Heck Coupling Reactions](http://article.sapub.org/image/10.5923.j.chemistry.20190902.03_010.gif)
Synthesis and Catalytic Activity of Palladium Mediated Metallodendrimer for the Sonogashira and Heck Coupling Reactions
Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in t
![C–N Cross-coupling Reactions of Amines with Aryl Halides Using Amide-Based Pincer Nickel(II) Catalyst | SpringerLink C–N Cross-coupling Reactions of Amines with Aryl Halides Using Amide-Based Pincer Nickel(II) Catalyst | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10562-019-03062-5/MediaObjects/10562_2019_3062_Figa_HTML.png)
C–N Cross-coupling Reactions of Amines with Aryl Halides Using Amide-Based Pincer Nickel(II) Catalyst | SpringerLink
![Influence of water/DMSO ratio on reaction rate in palladium-catalyzed... | Download Scientific Diagram Influence of water/DMSO ratio on reaction rate in palladium-catalyzed... | Download Scientific Diagram](https://www.researchgate.net/profile/Gerd_Jan_Ten_Brink/publication/303237422/figure/fig1/AS:366698319368192@1464439100629/Influence-of-water-DMSO-ratio-on-reaction-rate-in-palladium-catalyzed-oxidation-of.png)
Influence of water/DMSO ratio on reaction rate in palladium-catalyzed... | Download Scientific Diagram
![Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML](https://www.mdpi.com/catalysts/catalysts-10-00111/article_deploy/html/images/catalysts-10-00111-sch014-550.jpg)
Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML
![PDF) Reaction-Activated Palladium Catalyst for Dehydrogenation of Substituted Cyclohexanones to Phenols and H2 without Oxidants and Hydrogen Acceptors PDF) Reaction-Activated Palladium Catalyst for Dehydrogenation of Substituted Cyclohexanones to Phenols and H2 without Oxidants and Hydrogen Acceptors](https://www.researchgate.net/publication/277023994/figure/fig1/AS:614119296229418@1523428858574/Scheme-1-Dehydrogenation-of-substituted-cyclohexanones-to-phenols-The-reactions-of-both_Q320.jpg)
PDF) Reaction-Activated Palladium Catalyst for Dehydrogenation of Substituted Cyclohexanones to Phenols and H2 without Oxidants and Hydrogen Acceptors
![Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML](https://www.mdpi.com/catalysts/catalysts-10-00111/article_deploy/html/images/catalysts-10-00111-sch009.png)
Catalysts | Free Full-Text | The Reims Journey Towards Discovery and Understanding of Pd-Catalyzed Oxidations | HTML
![Regioselective synthesis of 2,3-disubstituted 1-alkyl pyrrolo[2,3-b] quinoxalines through palladium-catalyzed Heck reaction of chalcones and evaluation of their anti-bacterial activities - ScienceDirect Regioselective synthesis of 2,3-disubstituted 1-alkyl pyrrolo[2,3-b] quinoxalines through palladium-catalyzed Heck reaction of chalcones and evaluation of their anti-bacterial activities - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402018303284-fx1.jpg)
Regioselective synthesis of 2,3-disubstituted 1-alkyl pyrrolo[2,3-b] quinoxalines through palladium-catalyzed Heck reaction of chalcones and evaluation of their anti-bacterial activities - ScienceDirect
![Mild aromatic palladium-catalyzed protodecarboxylation: kinetic assessment of the decarboxylative palladation and the protodepalladation steps. - Abstract - Europe PMC Mild aromatic palladium-catalyzed protodecarboxylation: kinetic assessment of the decarboxylative palladation and the protodepalladation steps. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3686493/bin/nihms471691f16.jpg)
Mild aromatic palladium-catalyzed protodecarboxylation: kinetic assessment of the decarboxylative palladation and the protodepalladation steps. - Abstract - Europe PMC
![Design and Syntheses of Palladium Complexes of NNN/CNN Pincer Ligands: Catalyst for Cross Dehydrogenative Coupling Reaction of Heteroarenes - Organometallics - X-MOL Design and Syntheses of Palladium Complexes of NNN/CNN Pincer Ligands: Catalyst for Cross Dehydrogenative Coupling Reaction of Heteroarenes - Organometallics - X-MOL](https://xpic.x-mol.com/20200114%2F10.1021_acs.organomet.9b00695.gif)