![Organics | Free Full-Text | Palladium Catalyzed Ring-Opening of Diazabicylic Olefins with 4-Halo-1,3-Dicarbonyl Compounds: Accessing 3(2H)-Furanone-Appended Cyclopentenes Organics | Free Full-Text | Palladium Catalyzed Ring-Opening of Diazabicylic Olefins with 4-Halo-1,3-Dicarbonyl Compounds: Accessing 3(2H)-Furanone-Appended Cyclopentenes](https://www.mdpi.com/organics/organics-04-00006/article_deploy/html/images/organics-04-00006-g006.png)
Organics | Free Full-Text | Palladium Catalyzed Ring-Opening of Diazabicylic Olefins with 4-Halo-1,3-Dicarbonyl Compounds: Accessing 3(2H)-Furanone-Appended Cyclopentenes
The Use of Palladium Catalysis for the Formation of Fused Aromatic Compounds and for the Diastereoselective Formate Reduction of
![Molecules | Free Full-Text | Alkyl Levulinates and 2-Methyltetrahydrofuran: Possible Biomass-Based Solvents in Palladium-Catalyzed Aminocarbonylation Molecules | Free Full-Text | Alkyl Levulinates and 2-Methyltetrahydrofuran: Possible Biomass-Based Solvents in Palladium-Catalyzed Aminocarbonylation](https://pub.mdpi-res.com/molecules/molecules-28-00442/article_deploy/html/images/molecules-28-00442-ag.png?1672741960)
Molecules | Free Full-Text | Alkyl Levulinates and 2-Methyltetrahydrofuran: Possible Biomass-Based Solvents in Palladium-Catalyzed Aminocarbonylation
![Oxidative cross-coupling of allyl(trimethyl)silanes with aryl boronic acids by palladium catalysis - ScienceDirect Oxidative cross-coupling of allyl(trimethyl)silanes with aryl boronic acids by palladium catalysis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402018312778-fx1.jpg)
Oxidative cross-coupling of allyl(trimethyl)silanes with aryl boronic acids by palladium catalysis - ScienceDirect
![Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja1030936/asset/images/medium/ja-2010-030936_0012.gif)
Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society
![Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-020-19508-z/MediaObjects/41467_2020_19508_Fig1_HTML.png)
Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications
![Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja1030936/asset/images/medium/ja-2010-030936_0001.gif)
Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2 Catalyst System: Insights into the Effect of Naphthoquinone | Journal of the American Chemical Society
![Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms11806/MediaObjects/41467_2016_Article_BFncomms11806_Fig5_HTML.jpg)
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications
![Sulfonamide- and hydrazine-based palladium catalysts: Stable and efficient catalysts for C–C coupling reactions in aqueous medium - ScienceDirect Sulfonamide- and hydrazine-based palladium catalysts: Stable and efficient catalysts for C–C coupling reactions in aqueous medium - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116906014506-fx1.jpg)
Sulfonamide- and hydrazine-based palladium catalysts: Stable and efficient catalysts for C–C coupling reactions in aqueous medium - ScienceDirect
![Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/35bfa0cb-ad6d-456e-b543-dea1f7404d80/mcontent.jpg)
Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library
Palladium-Catalyzed Carbonylation of (Hetero)Aryl, Alkenyl and Allyl Halides by Means of N-Hydroxysuccinimidyl Formate as CO Surrogate | The Journal of Organic Chemistry
![Palladium-Catalyzed Carbonylation of (Hetero)Aryl, Alkenyl and Allyl Halides by Means of N-Hydroxysuccinimidyl Formate as CO Surrogate | The Journal of Organic Chemistry Palladium-Catalyzed Carbonylation of (Hetero)Aryl, Alkenyl and Allyl Halides by Means of N-Hydroxysuccinimidyl Formate as CO Surrogate | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.5b01119/asset/images/large/jo-2015-01119r_0006.jpeg)