Bis(triphenylphosphine)palladium chloride - Wikipedia
Molecules | Free Full-Text | Porphyrin/Chlorin Derivatives as Promising Molecules for Therapy of Colorectal Cancer | HTML
Phosphines
Palladium-Catalyzed Coupling of Hydroxylamines with Aryl Bromides, Chlorides, and Iodides | Organic Letters
Metal–Organic Frameworks with Low‐Valent Metal Nodes - Sikma - Angewandte Chemie - Wiley Online Library
Recent Developments in the Preparation and Chemistry of Metallacycles and Metallacages via Coordination | Chemical Reviews
Bis tris(2-methylphenyl)phosphine palladium 97 69861-71-8
Phosphine Oxides from a Medicinal Chemist's Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery | Journal of Medicinal Chemistry
Catalysts | Free Full-Text | Heck Reaction—State of the Art | HTML
Physical properties of porphyrin-based crystalline metal‒organic frameworks | Communications Chemistry
Recyclable Heterogeneous Palladium-Catalyzed Cyclocarbonylation of 2-Iodoanilines with Acyl Chlorides in the Biomass-Derived Solvent 2-Methyltetrahydrofuran | The Journal of Organic Chemistry
NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides | Journal of the American Chemical Society
Palladium--tri(propan-2-yl)phosphane (1/2) | C18H42P2Pd - PubChem
Palladium-Catalyzed C(sp3)–H Arylation of Diarylmethanes at Room Temperature: Synthesis of Triarylmethanes via Deprotonative-Cross-Coupling Processes | Journal of the American Chemical Society
NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides | Journal of the American Chemical Society
Modern Approaches in the Synthesis of Noble Metal Porphyrins for Their Practical Application (Review) | SpringerLink
Bis tris(2-methylphenyl)phosphine palladium 97 69861-71-8
Catalog
Hyper-stable organo-EuIII luminophore under high temperature for photo-industrial application | Scientific Reports
Bis(triphenylphosphine)palladium(II) dichloride 13965-03-2
![14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・206-18391・202-18393・204-18392[Detail Information] | [Synthesis & Materials]|Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation](https://labchem-wako.fujifilm.com/sc/01/14221-01-3.png "14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・206-18391・202-18393・204-18392[Detail Information] | [Synthesis & Materials]|Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation")
14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・206-18391・202-18393・204-18392[Detail Information] | [Synthesis & Materials]|Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation
Phosphine Oxides from a Medicinal Chemist's Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery | Journal of Medicinal Chemistry
Cyclometalated group-16 compounds of palladium and platinum: Challenges and opportunities - ScienceDirect
Catalysts | Free Full-Text | Synthesis of Indoles via Intermolecular and Intramolecular Cyclization by Using Palladium-Based Catalysts | HTML
η4-Tetrafluorobenzobarrelene)-η1-((tri-4-fluorophenyl)phosphine)-η1-(2-phenylphenyl)rhodium(I): A Catalyst for the Living Polymerization of Phenylacetylenes | Macromolecules
ABC‐Type meso‐Triaryl‐Substituted Subporphyrins - Yoshida - 2014 - European Journal of Organic Chemistry - Wiley Online Library
Acronyms
