PDF) Palladium-Catalyzed Dehydrogenative C-2 Alkenylation of 5-Arylimidazoles and Related Azoles with Styrenes
Fabrication of a metal free catalyst for chemical reactions through decoration of chitosan with ionic liquid terminated dendritic moiety | Scientific Reports
Efficient and Recyclable Solid-Supported Pd(II) Catalyst for Microwave-Assisted Suzuki Cross-Coupling in Aqueous Medium | ACS Omega
1-Butyl-3-Methylimidazolium - an overview | ScienceDirect Topics
A suitable modified palladium immobilized on imidazolium supported ionic liquid catalysed transfer hydrogenation of nitroarenes - ScienceDirect
Ligand‐Controlled Palladium‐Catalyzed Carbonylation of Alkynols: Highly Selective Synthesis of α‐Methylene‐β‐Lactones - Ge - 2020 - Angewandte Chemie International Edition - Wiley Online Library
Palladium-catalyzed ionic liquid-accelerated oxidative annulation of acetylenic oximes with unactivated long-chain enols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC02037K
![Kinetics, mechanism and density functional theory calculations on base hydrolysis of α-amino acid esters catalyzed by [Pd(AEMP)(H2O)2]2+ (AEMP = 2-(2-aminoethyl)-1-methylpyrrolidine) | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11144-020-01734-7/MediaObjects/11144_2020_1734_Figa_HTML.png "Kinetics, mechanism and density functional theory calculations on base hydrolysis of α-amino acid esters catalyzed by [Pd(AEMP)(H2O)2]2+ (AEMP = 2-(2-aminoethyl)-1-methylpyrrolidine) | SpringerLink")
Kinetics, mechanism and density functional theory calculations on base hydrolysis of α-amino acid esters catalyzed by [Pd(AEMP)(H2O)2]2+ (AEMP = 2-(2-aminoethyl)-1-methylpyrrolidine) | SpringerLink
Tuning the Size and Geometry of Pd(II)-Based Metallacalixarenes by Varying the N-Containing Ligands: Synthesis, Structure, and Sensing Properties | Crystal Growth & Design
A suitable modified palladium immobilized on imidazolium supported ionic liquid catalysed transfer hydrogenation of nitroarenes - ScienceDirect
1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols | ACS Sustainable Chemistry & Engineering
Direct fluorogenic detection of palladium and platinum organometallic complexes with proteins and nucleic acids in polyacrylamide gels | Scientific Reports
Shape-Controllable Formation of Poly-imidazolium Salts for Stable Palladium N-Heterocyclic Carbene Polymers | Scientific Reports
26218-78-0|Methyl 6-bromonicotinate| Ambeed
A suitable modified palladium immobilized on imidazolium supported ionic liquid catalysed transfer hydrogenation of nitroarenes - ScienceDirect
Crystal structure of 1,1′-(hexane-1,6-diyl)bis(3-methyl-1H-imidazol-3-ium) bis(hexafluoro phosphate), C14H24F12N4P2
Imidazolium-urea low transition temperature mixtures for the UHP-promoted oxidation of boron compounds - ScienceDirect
N-Heterocyclic Carbene–Palladium(II)–1-Methylimidazole Complex-Catalyzed Suzuki–Miyaura Coupling of Aryl Sulfonates with Arylboronic Acids | The Journal of Organic Chemistry
1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols | ACS Sustainable Chemistry & Engineering
6153-44-2|Methyl 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate| Ambeed
Recent Advances in Pd‐Catalyzed Cross‐Coupling Reaction in Ionic Liquids - Li - 2018 - European Journal of Organic Chemistry - Wiley Online Library
Palladium-Catalyzed Transformations of Alkyl C–H Bonds | Chemical Reviews
Recent Advances in Pd‐Catalyzed Cross‐Coupling Reaction in Ionic Liquids - Li - 2018 - European Journal of Organic Chemistry - Wiley Online Library
Catalysts | Free Full-Text | Immobilized Palladium Nanoparticles on Zirconium Carboxy-Aminophosphonates Nanosheets as an Efficient Recoverable Heterogeneous Catalyst for Suzuki–Miyaura and Heck Coupling
Polymer-Supported N-Heterocyclic Carbene−Palladium Complex for Heterogeneous Suzuki Cross-Coupling Reaction | The Journal of Organic Chemistry
