![Tuning the Selectivity of Palladium Catalysts for Hydroformylation and Semihydrogenation of Alkynes: Experimental and Mechanistic Studies - ACS Catal. - X-MOL Tuning the Selectivity of Palladium Catalysts for Hydroformylation and Semihydrogenation of Alkynes: Experimental and Mechanistic Studies - ACS Catal. - X-MOL](https://xpic.x-mol.com/20201006%2F10.1021_acscatal.0c03614.gif)
Tuning the Selectivity of Palladium Catalysts for Hydroformylation and Semihydrogenation of Alkynes: Experimental and Mechanistic Studies - ACS Catal. - X-MOL
![Second-Generation Palladium Catalyst System for Transannular C–H Functionalization of Azabicycloalkanes - J. Am. Chem. Soc. - X-MOL Second-Generation Palladium Catalyst System for Transannular C–H Functionalization of Azabicycloalkanes - J. Am. Chem. Soc. - X-MOL](https://xpic.x-mol.com/paperImg%2F2020_03_12%2FJournal_of_the_American_Chemical_Society_All_img%2F10.1021_jacs.8b02142.gif)
Second-Generation Palladium Catalyst System for Transannular C–H Functionalization of Azabicycloalkanes - J. Am. Chem. Soc. - X-MOL
![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-g001.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
![A highly efficient palladium( ii )/polyoxometalate catalyst system for aerobic oxidation of alcohols - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY01632G A highly efficient palladium( ii )/polyoxometalate catalyst system for aerobic oxidation of alcohols - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY01632G](https://pubs.rsc.org/image/article/2015/CY/c4cy01632g/c4cy01632g-f1_hi-res.gif)
A highly efficient palladium( ii )/polyoxometalate catalyst system for aerobic oxidation of alcohols - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY01632G
![Conversion and yield of hydrogenation with TRISO ®-palladium catalyst... | Download Scientific Diagram Conversion and yield of hydrogenation with TRISO ®-palladium catalyst... | Download Scientific Diagram](https://www.researchgate.net/profile/Matthias_Nuechter/publication/26538381/figure/fig7/AS:669957058723844@1536741618190/Conversion-and-yield-of-hydrogenation-with-TRISO-R-palladium-catalyst-system-of.png)
Conversion and yield of hydrogenation with TRISO ®-palladium catalyst... | Download Scientific Diagram
![J Org Chem/Org Lett a Twitter: "The addition of NaF has enabled the regeneration of hafnocene difluoride and zirconocene difluoride, leading to achievement of a bimetallic catalytic system with a palladium catalyst--a J Org Chem/Org Lett a Twitter: "The addition of NaF has enabled the regeneration of hafnocene difluoride and zirconocene difluoride, leading to achievement of a bimetallic catalytic system with a palladium catalyst--a](https://pbs.twimg.com/media/DqSZyh-WoAAtPFn.jpg)
J Org Chem/Org Lett a Twitter: "The addition of NaF has enabled the regeneration of hafnocene difluoride and zirconocene difluoride, leading to achievement of a bimetallic catalytic system with a palladium catalyst--a
![A new palladium catalyst system for the cyanation of aryl chlorides with K4[Fe(CN)6] | Sigma-Aldrich A new palladium catalyst system for the cyanation of aryl chlorides with K4[Fe(CN)6] | Sigma-Aldrich](https://www.sigmaaldrich.com/content/dam/sigma-aldrich/chemistry/chemical-synthesis/catalysis/35-prd.jpg)
A new palladium catalyst system for the cyanation of aryl chlorides with K4[Fe(CN)6] | Sigma-Aldrich
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig1_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
Development of (quinolinyl)amido-based pincer palladium complexes: a robust and phosphine-free catalyst system for C–H arylation of benzothiazoles - New Journal of Chemistry (RSC Publishing)
![PDF) A Palladium Catalyst System for the Efficient Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid: Synthesis and Biological Activity Evaluation PDF) A Palladium Catalyst System for the Efficient Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid: Synthesis and Biological Activity Evaluation](https://i1.rgstatic.net/publication/328278360_A_Palladium_Catalyst_System_for_the_Efficient_Cross-Coupling_Reaction_of_Aryl_Bromides_and_Chlorides_with_Phenylboronic_Acid_Synthesis_and_Biological_Activity_Evaluation/links/5cfffba9299bf13a384e744b/largepreview.png)
PDF) A Palladium Catalyst System for the Efficient Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid: Synthesis and Biological Activity Evaluation
![Silica Supported Molecular Palladium Catalyst for Selective Hydrodeoxygenation of Aromatic Compounds under Mild Conditions - ACS Catal. - X-MOL Silica Supported Molecular Palladium Catalyst for Selective Hydrodeoxygenation of Aromatic Compounds under Mild Conditions - ACS Catal. - X-MOL](https://xpic.x-mol.com/20190907%2F10.1021_acscatal.9b02460.jpg)
Silica Supported Molecular Palladium Catalyst for Selective Hydrodeoxygenation of Aromatic Compounds under Mild Conditions - ACS Catal. - X-MOL
![Palladium catalyzed methoxycarbonylation of 1-dodecene in biphasic systems – Optimization of catalyst recycling - ScienceDirect Palladium catalyzed methoxycarbonylation of 1-dodecene in biphasic systems – Optimization of catalyst recycling - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2468823117303218-fx1.jpg)
Palladium catalyzed methoxycarbonylation of 1-dodecene in biphasic systems – Optimization of catalyst recycling - ScienceDirect
![Sustainable and recyclable heterogenous palladium catalysts from rice husk-derived biosilicates for Suzuki-Miyaura cross-couplings, aerobic oxidations and stereoselective cascade carbocyclizations | Scientific Reports Sustainable and recyclable heterogenous palladium catalysts from rice husk-derived biosilicates for Suzuki-Miyaura cross-couplings, aerobic oxidations and stereoselective cascade carbocyclizations | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-020-63083-8/MediaObjects/41598_2020_63083_Fig1_HTML.png)
Sustainable and recyclable heterogenous palladium catalysts from rice husk-derived biosilicates for Suzuki-Miyaura cross-couplings, aerobic oxidations and stereoselective cascade carbocyclizations | Scientific Reports
![PDF) Green Chemistry Adapting a Wacker-type catalyst system to the palladium-catalyzed oxidative carbonylation of aliphatic polyols | Thomas E Müller - Academia.edu PDF) Green Chemistry Adapting a Wacker-type catalyst system to the palladium-catalyzed oxidative carbonylation of aliphatic polyols | Thomas E Müller - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/46713951/mini_magick20190209-10589-1ust6gq.png?1549700807)
PDF) Green Chemistry Adapting a Wacker-type catalyst system to the palladium-catalyzed oxidative carbonylation of aliphatic polyols | Thomas E Müller - Academia.edu
Tailored Cationic Palladium( 11) Compounds as Catalysts for Highly Selective Dimerization and Polymerization of Vinylic Monomers
Pd-PEPPSI-IPentCl: a new highly efficient ligand-free and recyclable catalyst system for the synthesis of 2-substituted indoles via domino copper-free Sonogashira coupling/cyclization - New Journal of Chemistry (RSC Publishing)
![Catalysts | Free Full-Text | Recent Advances in Metal-Catalyzed Alkyl–Boron (C(sp3)–C(sp2)) Suzuki-Miyaura Cross-Couplings | HTML Catalysts | Free Full-Text | Recent Advances in Metal-Catalyzed Alkyl–Boron (C(sp3)–C(sp2)) Suzuki-Miyaura Cross-Couplings | HTML](https://www.mdpi.com/catalysts/catalysts-10-00296/article_deploy/html/images/catalysts-10-00296-sch001.png)
Catalysts | Free Full-Text | Recent Advances in Metal-Catalyzed Alkyl–Boron (C(sp3)–C(sp2)) Suzuki-Miyaura Cross-Couplings | HTML
![Active catalyst system in carboxytelomerisation of 1,3-butadiene with... | Download Scientific Diagram Active catalyst system in carboxytelomerisation of 1,3-butadiene with... | Download Scientific Diagram](https://www.researchgate.net/publication/337390844/figure/fig2/AS:883324029526016@1587612268216/Active-catalyst-system-in-carboxytelomerisation-of-1-3-butadiene-with-methanol-comprising.png)
Active catalyst system in carboxytelomerisation of 1,3-butadiene with... | Download Scientific Diagram
![Supported Palladium on Magnetic Nanoparticles–Starch Substrate (Pd-MNPSS): Highly Efficient Magnetic Reusable Catalyst for C–C Coupling Reactions in Water - ACS Sustainable Chem. Eng. - X-MOL Supported Palladium on Magnetic Nanoparticles–Starch Substrate (Pd-MNPSS): Highly Efficient Magnetic Reusable Catalyst for C–C Coupling Reactions in Water - ACS Sustainable Chem. Eng. - X-MOL](https://xpic.x-mol.com/20171216%2F10.1021_acssuschemeng.7b03923.jpg)
Supported Palladium on Magnetic Nanoparticles–Starch Substrate (Pd-MNPSS): Highly Efficient Magnetic Reusable Catalyst for C–C Coupling Reactions in Water - ACS Sustainable Chem. Eng. - X-MOL
![A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling | Nature Nanotechnology A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling | Nature Nanotechnology](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41565-018-0167-2/MediaObjects/41565_2018_167_Fig1_HTML.jpg)
A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling | Nature Nanotechnology
![Catalytic Transfer Hydrodebenzylation with Low Palladium Loading - Yakukhnov - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library Catalytic Transfer Hydrodebenzylation with Low Palladium Loading - Yakukhnov - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/0212f797-4138-4843-989c-a786196e4558/adsc201900686-toc-0001-m.jpg)
Catalytic Transfer Hydrodebenzylation with Low Palladium Loading - Yakukhnov - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
![UV-irradiation-mediated palladium nanoparticle catalytic system: Heck and decarboxylative coupling reactions - ScienceDirect UV-irradiation-mediated palladium nanoparticle catalytic system: Heck and decarboxylative coupling reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2468823117304054-fx1.jpg)