Oxygen-Promoted Suzuki–Miyaura Reaction for Efficient Construction of Biaryls

DOI: 10.1002/tcr.201500218

Linear scaling relationships and volcano plots in homogeneous catalysis – revisiting the Suzuki reaction

DOI: 10.1039/C5SC02910D

Selection of boron reagents for Suzuki–Miyaura coupling

Suzuki-Miyaura Cross-Coupling of Unprotected, Nitrogen-Rich Heterocycles: Substrate Scope and Mechanistic Investigation

Transmetalation in the Suzuki–Miyaura Coupling: The Fork in the Trail

DOI: 10.1002/anie.201301737

A convenient one-pot access to phenanthridinones via Suzuki-Miyaura cross-coupling reaction

Palladium-Catalyzed Decarboxylative Suzuki and Heck Couplings of Azaindole-2-carboxylic Acids: Synthesis of 2-Aryl/Alkenyl-1-phenylsulfonyl-1 H-pyrrolo-[2,3 b]pyridines

Keep stirring that Suzuki

A wonder full finding: Small thinks make big difference in results!!

Mechanistic Investigations of a Palladium-Diene Catalyzed Suzuki–Miyaura Cross-Coupling Reaction

Regioselective and Stereospecific Cross-Coupling of Primary Allylic Amines with Boronic Acids and Boronates through Palladium-Catalyzed C[BOND]N Bond Cleavage

Use of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalysts

Chem. Commun., 2012, 48, 2912-2914

The Triple Role of Fluoride Ions in Palladium-Catalyzed Suzuki–Miyaura Reactions: Unprecedented Transmetalation from [ArPdFL2] Complexes

Inversion or Retention? Effects of Acidic Additives on the Stereochemical Course in Enantiospecific Suzuki–Miyaura Coupling of α-(Acetylamino)benzylboronic Esters

DOI: 10.1021/ja210025q

Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki–Miyaura Cross-Coupling Reaction

DOI: 10.1002/adsc.201100531

Nickel-Catalyzed Suzuki–Miyaura Reaction of Aryl Fluorides

Naoto Chatani, JACS, 2011, DOI: 10.1021/ja207759e

An efficient and simple protocol for a PdCl2-ligandless and additive-free Suzuki coupling reaction of aryl bromides

doi:10.1016/j.tetlet.2011.09.115