![PDF) Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols | Vishal Purohit - Academia.edu PDF) Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols | Vishal Purohit - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/47399290/mini_magick20190206-25682-1nngxlm.png?1549524805)
PDF) Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols | Vishal Purohit - Academia.edu
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)
Tuning the Catalytic Activity and Selectivity of Pd Nanoparticles Using Ligand-Modified Supports and Surfaces
![Palladium/Nucleophilic Carbene Catalysts for Cross-Coupling Reactions | Johnson Matthey Technology Review Palladium/Nucleophilic Carbene Catalysts for Cross-Coupling Reactions | Johnson Matthey Technology Review](https://www.technology.matthey.com/images/articles/46/2/pmr0046-fig1.gif)
Palladium/Nucleophilic Carbene Catalysts for Cross-Coupling Reactions | Johnson Matthey Technology Review
![Catalysts | Free Full-Text | Oxidation of Thiol Using Ionic Liquid-Supported Organotelluride as a Recyclable Catalyst | HTML Catalysts | Free Full-Text | Oxidation of Thiol Using Ionic Liquid-Supported Organotelluride as a Recyclable Catalyst | HTML](https://www.mdpi.com/catalysts/catalysts-10-00398/article_deploy/html/images/catalysts-10-00398-g001-550.jpg)
Catalysts | Free Full-Text | Oxidation of Thiol Using Ionic Liquid-Supported Organotelluride as a Recyclable Catalyst | HTML
![Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science](https://science.sciencemag.org/content/sci/356/6342/1059/F1.large.jpg?width=800&height=600&carousel=1)
Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science
![Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402016300126-fx1.jpg)
Palladium N-heterocyclic carbene catalyzed regioselective thiolation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using aryl thiols - ScienceDirect
![Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S245192941830072X-gr3.jpg)
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect
![Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing) Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)](https://pubs.rsc.org/image/article/2018/cy/c8cy00173a/c8cy00173a-s4_hi-res.gif)
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)
![Catalysts | Free Full-Text | The Combination of Lewis Acid with N-Heterocyclic Carbene (NHC) Catalysis | HTML Catalysts | Free Full-Text | The Combination of Lewis Acid with N-Heterocyclic Carbene (NHC) Catalysis | HTML](https://www.mdpi.com/catalysts/catalysts-09-00863/article_deploy/html/images/catalysts-09-00863-sch001.png)
Catalysts | Free Full-Text | The Combination of Lewis Acid with N-Heterocyclic Carbene (NHC) Catalysis | HTML
![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-sch034.png)
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![Application of Thiol-Modified Dual-Pore Silica Beads as a Practical Scavenger of Leached Palladium Catalyst in C–C Coupling Reactions - Org. Process Res. Dev. - X-MOL Application of Thiol-Modified Dual-Pore Silica Beads as a Practical Scavenger of Leached Palladium Catalyst in C–C Coupling Reactions - Org. Process Res. Dev. - X-MOL](https://xpic.x-mol.com/20190207%2F10.1021_acs.oprd.8b00291.jpg)
Application of Thiol-Modified Dual-Pore Silica Beads as a Practical Scavenger of Leached Palladium Catalyst in C–C Coupling Reactions - Org. Process Res. Dev. - X-MOL
![Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S245192941830072X-fx1.jpg)
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect
![A novel tetrazole functionalized polymer-supported palladium nano-catalyst for the synthesis of various N-benzylated arylcyanamides - J. Alloys Compd. - X-MOL A novel tetrazole functionalized polymer-supported palladium nano-catalyst for the synthesis of various N-benzylated arylcyanamides - J. Alloys Compd. - X-MOL](https://xpic.x-mol.com/20180525%2F10.1016_j.jallcom.2018.05.271.jpg)
A novel tetrazole functionalized polymer-supported palladium nano-catalyst for the synthesis of various N-benzylated arylcyanamides - J. Alloys Compd. - X-MOL
![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-gf11.jpg)
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
![Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium: Selective Formation of cis‐Configured Vinyl Thioethers - Gerber - 2012 - Chemistry – A European Journal - Wiley Online Library Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium: Selective Formation of cis‐Configured Vinyl Thioethers - Gerber - 2012 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/4e68c49e-bdc7-4a6f-b8a9-907904e36461/mcontent.jpg)
Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium: Selective Formation of cis‐Configured Vinyl Thioethers - Gerber - 2012 - Chemistry – A European Journal - Wiley Online Library
![PDF) Polymer-Supported Palladium(II) Carbene Complexes: Catalytic Activity, Recyclability, and Selectivity in C-H Acetoxylation of Arenes PDF) Polymer-Supported Palladium(II) Carbene Complexes: Catalytic Activity, Recyclability, and Selectivity in C-H Acetoxylation of Arenes](https://i1.rgstatic.net/publication/316266086_Polymer-Supported_PalladiumII_Carbene_Complexes_Catalytic_Activity_Recyclability_and_Selectivity_in_C-H_Acetoxylation_of_Arenes/links/5abb5fdaa6fdcc716470a51b/largepreview.png)
PDF) Polymer-Supported Palladium(II) Carbene Complexes: Catalytic Activity, Recyclability, and Selectivity in C-H Acetoxylation of Arenes
![Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry - Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/37e541f1-e9bd-4b25-95f4-0ccd086d28fc/mfig000.jpg)
Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -
![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)