Triphenylphosphine chalcogenides as efficient ligands for room temperature palladium(II)-catalyzed Suzuki–Miyaura reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference42 articles.
1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
2. Ligand-free Suzuki–Miyaura reaction catalysed by Pd/C at room temperature
3. Efficient Protocol for the Phosphine-Free Suzuki-Miyaura Reaction Catalyzed by Palladium on Carbon at Room Temperature
4. Pd/C: An Old Catalyst for New Applications – Its Use for the Suzuki–Miyaura Reaction
5. Ion- and Atom-Leaching Mechanisms from Palladium Nanoparticles in Cross-Coupling Reactions
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1. A tertiary phosphine oxide ligand-based recyclable system for the Suzuki–Miyaura and Negishi reactions: evidence for pseudo-homogeneous catalysis;Catalysis Science & Technology;2023
2. Catalyst‐ and Solvent‐Free Hydrophosphorylation of Aldimines with Secondary Phosphine Chalcogenides: Synthesis of Tertiary α ‐Aminophosphine Oxides, Sulfides and Selenides;ChemistrySelect;2022-12
3. Efficient and Recyclable Solid-Supported Pd(II) Catalyst for Microwave-Assisted Suzuki Cross-Coupling in Aqueous Medium;ACS Omega;2022-08-10
4. Magnetically recyclable Schiff-based palladium nanocatalyst [Fe3O4@SiNSB-Pd] and its catalytic applications in Heck reaction;Arabian Journal of Chemistry;2022-07
5. Improved Suzuki–Miyaura reaction conversion efficiency using magnetic nanoparticles and inductive heating;Journal of Materials Science;2022-01
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