Modern Approaches in the Synthesis of Noble Metal Porphyrins for Their Practical Application (Review) | SpringerLink
Palladium-Catalyzed Coupling of Hydroxylamines with Aryl Bromides, Chlorides, and Iodides | Organic Letters
Hyper-stable organo-EuIII luminophore under high temperature for photo-industrial application | Scientific Reports
Phosphine Oxides from a Medicinal Chemist's Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery | Journal of Medicinal Chemistry
Acronyms
Physical properties of porphyrin-based crystalline metal‒organic frameworks | Communications Chemistry
Catalysts | Free Full-Text | Synthesis of Indoles via Intermolecular and Intramolecular Cyclization by Using Palladium-Based Catalysts | HTML
Catalysts | Free Full-Text | Heck Reaction—State of the Art | HTML
NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides | Journal of the American Chemical Society
Phosphines
ABC‐Type meso‐Triaryl‐Substituted Subporphyrins - Yoshida - 2014 - European Journal of Organic Chemistry - Wiley Online Library
Catalysts | Free Full-Text | Heck Reaction—State of the Art | HTML
Bis(triphenylphosphine)palladium chloride - Wikipedia
Cocrystallization-driven stabilization of metastable nanoclusters: a case study of Pd 1 Au 9 - Nanoscale (RSC Publishing) DOI:10.1039/D1NR00721A
Bis tris(2-methylphenyl)phosphine palladium 97 69861-71-8
Bis tris(2-methylphenyl)phosphine palladium 97 69861-71-8
Molecules | Free Full-Text | Porphyrin/Chlorin Derivatives as Promising Molecules for Therapy of Colorectal Cancer | HTML
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
Metal–Organic Frameworks with Low‐Valent Metal Nodes - Sikma - Angewandte Chemie - Wiley Online Library
NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides | Journal of the American Chemical Society
Tertiary phosphines: preparation and reactivity (RSC Publishing) DOI:10.1039/9781788019491-00001