Magnetic nanoparticles supported N-heterocyclic palladium complex: Synthesis and catalytic evaluations in Suzuki cross-coupling reaction - ScienceDirect
BJOC - A novel 4-aminoantipyrine-Pd(II) complex catalyzes Suzuki–Miyaura cross-coupling reactions of aryl halides
Palladium-Schiff Base Complex Immobilized Covalently on Magnetic Nanoparticles as an Efficient and Recyclable Catalyst for Heck and Suzuki Cross-Coupling Reactions | SpringerLink
Suzuki–Miyaura cross coupling reaction: recent advancements in catalysis and organic synthesis - Catalysis Science & Technology (RSC Publishing)
Application of Palladium-Catalyzed Cross-Coupling Reactions in Organic Synthesis | Bentham Science
![Synthesis of Phenanthro[9,10‐d]imidazoles and their Potential Applications in Solution Processable Bottom‐Gated OFETs,Asian Journal of Organic Chemistry - X-MOL](https://xpic.x-mol.com/20200610%2F10.1002_ajoc.202000156.jpg "Synthesis of Phenanthro[9,10‐d]imidazoles and their Potential Applications in Solution Processable Bottom‐Gated OFETs,Asian Journal of Organic Chemistry - X-MOL")
Synthesis of Phenanthro[9,10‐d]imidazoles and their Potential Applications in Solution Processable Bottom‐Gated OFETs,Asian Journal of Organic Chemistry - X-MOL
Palladium supported on phosphinite functionalized Fe3O4 nanoparticles as a new magnetically separable catalyst for Suzuki–Miyaura coupling reactions in aqueous media - Catalysis Science & Technology (RSC Publishing)
Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update - Bhattacherjee - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library
PDF) Palladium(0) catalyzed Suzuki cross-coupling reaction of 2,5-dibromo-3-methylthiophene: selectivity, characterization, DFT studies and their biological evaluations
A thiosemicarbazone–palladium(II)–imidazole complex as an efficient pre- catalyst for Suzuki–Miyaura cross-coupling reactions at room temperature in aqueous media | SpringerLink
Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides | Nature Communications
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Suzuki–Miyaura cross coupling reaction: recent advancements in catalysis and organic synthesis - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/D0CY02059A
Suzuki-Miyaura Coupling Enabled by Aryl to Vinyl 1,4-Palladium Migration - ScienceDirect
A highly controllable, effective, and recyclable magnetic-nanoparticle-supported palladium catalyst for the Suzuki–Miyaura cross-coupling reaction - ScienceDirect
Visible-light-driven Photocatalytic N-arylation of Imidazole Derivatives and Arylboronic Acids on Cu/graphene catalyst | Scientific Reports
A robust polyfunctional Pd(II)-based magnetic amphiphilic nanocatalyst for the Suzuki–Miyaura coupling reaction | Scientific Reports
Imidazole containing palladium(II) complexes as efficient pre-catalyst systems for Heck and Suzuki coupling reaction: Synthesis, structural characterization and catalytic properties - ScienceDirect
The Suzuki-Miyaura coupling reactions of aryl halides with... | Download Table
Scheme 8 NHC-Pd(II) complexes were compared in Suzuki-Miyaura... | Download Scientific Diagram
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Molecules | Free Full-Text | Synthesis, Characterization and Microwave-Promoted Catalytic Activity of Novel N-phenylbenzimidazolium Salts in Heck-Mizoroki and Suzuki-Miyaura Cross-Coupling Reactions under Mild Conditions | HTML
Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update - Bhattacherjee - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library
NiFe2O4@SiO2@ZrO2/SO42−/Cu/Co nanoparticles: a novel, efficient, magnetically recyclable and bimetallic catalyst for Pd-free Suzuki, Heck and C–N cross-coupling reactions in aqueous media - New Journal of Chemistry (RSC Publishing)
Recent applications of the Suzuki–Miyaura cross-coupling reaction ...
