![The Palladium Acetate‐Catalyzed Microwave‐Assisted Hirao Reaction without an Added Phosphorus Ligand as a “Green” Protocol: A Quantum Chemical Study on the Mechanism - Keglevich - 2017 - Advanced Synthesis & Catalysis - The Palladium Acetate‐Catalyzed Microwave‐Assisted Hirao Reaction without an Added Phosphorus Ligand as a “Green” Protocol: A Quantum Chemical Study on the Mechanism - Keglevich - 2017 - Advanced Synthesis & Catalysis -](https://onlinelibrary.wiley.com/cms/asset/1f89e28f-55cf-4928-b6fe-ee08deb994dd/adsc201700895-toc-0001-m.jpg)
The Palladium Acetate‐Catalyzed Microwave‐Assisted Hirao Reaction without an Added Phosphorus Ligand as a “Green” Protocol: A Quantum Chemical Study on the Mechanism - Keglevich - 2017 - Advanced Synthesis & Catalysis -
![EP0921212A1 - Composition for electroplating palladium alloys and electroplating process using that composition - Google Patents EP0921212A1 - Composition for electroplating palladium alloys and electroplating process using that composition - Google Patents](https://patentimages.storage.googleapis.com/95/06/8e/62eec901f1f9c3/00090001.png)
EP0921212A1 - Composition for electroplating palladium alloys and electroplating process using that composition - Google Patents
![Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | HTML Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | HTML](https://www.mdpi.com/catalysts/catalysts-10-00136/article_deploy/html/images/catalysts-10-00136-g002.png)
Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | 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](http://www.scielo.br/img/revistas/jbchs/v25n12//0103-5053-jbchs-25-12-2186-gf44.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![logo A Publication of Reliable Methods for the Preparation of Organic Compounds Search Citation Search Text Annual Volume 97 96 95 94 93 92 91 90 89 88 87 86 85 84 83 82 81 80 79 78 77 76 75 74 73 72 71 70 69 68 67 66 65 64 63 62 61 60 59 58 57 ... logo A Publication of Reliable Methods for the Preparation of Organic Compounds Search Citation Search Text Annual Volume 97 96 95 94 93 92 91 90 89 88 87 86 85 84 83 82 81 80 79 78 77 76 75 74 73 72 71 70 69 68 67 66 65 64 63 62 61 60 59 58 57 ...](http://www.orgsyn.org/content/figures/v88p0377-4.gif)
logo A Publication of Reliable Methods for the Preparation of Organic Compounds Search Citation Search Text Annual Volume 97 96 95 94 93 92 91 90 89 88 87 86 85 84 83 82 81 80 79 78 77 76 75 74 73 72 71 70 69 68 67 66 65 64 63 62 61 60 59 58 57 ...
![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-gf01.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![Pd(OAc) 2 -catalyzed asymmetric hydrogenation of sterically hindered N -tosylimines | Nature Communications Pd(OAc) 2 -catalyzed asymmetric hydrogenation of sterically hindered N -tosylimines | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-018-07462-w/MediaObjects/41467_2018_7462_Fig1_HTML.png)
Pd(OAc) 2 -catalyzed asymmetric hydrogenation of sterically hindered N -tosylimines | Nature Communications
![Speciation of Pd(OAc)2 in ligandless Suzuki–Miyaura reactions - Catalysis Science & Technology (RSC Publishing) Speciation of Pd(OAc)2 in ligandless Suzuki–Miyaura reactions - Catalysis Science & Technology (RSC Publishing)](https://pubs.rsc.org/image/article/2012/cy/c1cy00241d/c1cy00241d-s4.gif)
Speciation of Pd(OAc)2 in ligandless Suzuki–Miyaura reactions - Catalysis Science & Technology (RSC Publishing)
![A mechanistic study of cross-coupling reactions catalyzed by palladium nanoparticles supported on polyaniline nanofibers - Inorganic Chemistry Frontiers (RSC Publishing) A mechanistic study of cross-coupling reactions catalyzed by palladium nanoparticles supported on polyaniline nanofibers - Inorganic Chemistry Frontiers (RSC Publishing)](https://pubs.rsc.org/image/article/2015/qi/c4qi00130c/c4qi00130c-f6_hi-res.gif)
A mechanistic study of cross-coupling reactions catalyzed by palladium nanoparticles supported on polyaniline nanofibers - Inorganic Chemistry Frontiers (RSC Publishing)
![The ubiquitous cross-coupling catalyst system 'Pd(OAc) 2 '/2PPh 3 forms a unique dinuclear Pd I complex: an important entry point into catalytically c ... - Chemical Science (RSC Publishing) DOI:10.1039/C9SC01847F The ubiquitous cross-coupling catalyst system 'Pd(OAc) 2 '/2PPh 3 forms a unique dinuclear Pd I complex: an important entry point into catalytically c ... - Chemical Science (RSC Publishing) DOI:10.1039/C9SC01847F](https://pubs.rsc.org/image/article/2019/SC/c9sc01847f/c9sc01847f-f6_hi-res.gif)
The ubiquitous cross-coupling catalyst system 'Pd(OAc) 2 '/2PPh 3 forms a unique dinuclear Pd I complex: an important entry point into catalytically c ... - Chemical Science (RSC Publishing) DOI:10.1039/C9SC01847F
![Ammonium Formate/Palladium on Carbon: A Versatile System for Catalytic Hydrogen Transfer Reductions of Carbon-Carbon Double Bonds Ammonium Formate/Palladium on Carbon: A Versatile System for Catalytic Hydrogen Transfer Reductions of Carbon-Carbon Double Bonds](https://www.organic-chemistry.org/abstracts/literature/250m.gif)
Ammonium Formate/Palladium on Carbon: A Versatile System for Catalytic Hydrogen Transfer Reductions of Carbon-Carbon Double Bonds
![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](https://www.mdpi.com/catalysts/catalysts-10-00004/article_deploy/html/images/catalysts-10-00004-sch001.png)
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/8c5b4a3e-4417-4dbb-aea2-5f84cd987f1d/chem201900451-fig-5001-m.jpg)
Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library
![Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/7f03d982-4216-47a2-81c7-ec1f4d660b42/chem201900451-fig-5003-m.jpg)
Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions - Wagschal - 2019 - Chemistry – A European Journal - Wiley Online Library
![Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | HTML Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | HTML](https://www.mdpi.com/catalysts/catalysts-10-00136/article_deploy/html/images/catalysts-10-00136-g013.png)
Catalysts | Free Full-Text | Recent Developments in the Immobilization of Palladium Complexes on Renewable Polysaccharides for Suzuki–Miyaura Cross-Coupling of Halobenzenes and Phenylboronic Acids | HTML
![Metal catalyzed defunctionalization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01949D Metal catalyzed defunctionalization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01949D](https://pubs.rsc.org/image/article/2016/OB/c5ob01949d/c5ob01949d-s32_hi-res.gif)