Emerging Trends in Cross-Coupling: Twelve-Electron-Based L1Pd(0) Catalysts, Their Mechanism of Action, and Selected Applications

SJ Firsan, V Sivakumar, TJ Colacot - Chemical Reviews, 2022 - ACS Publications
Monoligated palladium (0) species, L1Pd (0), have emerged as the most active catalytic
species in the cross-coupling cycle. Today, there are methods available to generate the …

Buchwald-Hartwig reaction: an overview

MM Heravi, Z Kheilkordi, V Zadsirjan, M Heydari… - Journal of …, 2018 - Elsevier
Pd-catalyzed amination reaction of aryl halides has attracted much attention in recent years.
This review underscores selected important recent developments in the catalysis of one of …

Recent developments in the Suzuki-Miyaura reaction: 2010–2014

I Maluenda, O Navarro - Molecules, 2015 - mdpi.com
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and
an organic halide or pseudo-halide in the presence of a palladium or nickel catalyst and a …

Electrochemical synthesis of biaryls by reductive extrusion from N,N'-diarylureas

E Stammers, CD Parsons, J Clayden… - Nature …, 2023 - nature.com
The synthesis of biaryl compounds by the transition-metal free coupling of arenes is an
important contemporary challenge, aiming to avoid the toxicity and cost profiles associated …

Generating active “L-Pd (0)” via neutral or cationic π-allylpalladium complexes featuring biaryl/bipyrazolylphosphines: synthetic, mechanistic, and structure–activity …

AJ DeAngelis, PG Gildner, R Chow… - The Journal of organic …, 2015 - ACS Publications
Two new classes of highly active yet air-and moisture-stable π-R-allylpalladium complexes
containing bulky biaryl-and bipyrazolylphosphines with extremely broad ligand scope have …

Virtual ligand strategy in transition metal catalysis toward highly efficient elucidation of reaction mechanisms and computational catalyst design

W Matsuoka, Y Harabuchi, S Maeda - ACS Catalysis, 2023 - ACS Publications
In the development of transition metal catalysis, the process of ligand screening, where an
optimal ligand for a reaction of interest is identified from a large variety of candidate …

Green Suzuki–Miyaura coupling reaction catalyzed by palladium nanoparticles supported on graphitic carbon nitride

J Sun, Y Fu, G He, X Sun, X Wang - Applied Catalysis B: Environmental, 2015 - Elsevier
The synthesis of biphenyls under mild conditions is really a challenge to green chemistry.
Here we report a facile photodeposition strategy to fabricate a Pd/gC 3 N 4 nanocomposite …

Rational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis

P Ruiz-Castillo, DG Blackmond… - Journal of the American …, 2015 - ACS Publications
We report the Pd-catalyzed arylation of very hindered α, α, α-trisubstituted primary amines.
Kinetics-based mechanistic analysis and rational design have led to the development of two …

It Is Not All about the Ligands: Exploring the Hidden Potentials of tBu3P through Its Oxidative Addition Complex as the Precatalyst

YN Timsina, G Xu, TJ Colacot - ACS Catalysis, 2023 - ACS Publications
A series of oxidative addition complexes with a general formula (t Bu3P) Pd (Ar) X, as a
class of precatalysts, were synthesized for challenging Suzuki–Miyaura coupling involving …

Functionalization of Imidazo[1,2‐a]pyridines by Means of Metal‐Catalyzed Cross‐Coupling Reactions

J Koubachi, S El Kazzouli, M Bousmina… - European Journal of …, 2014 - Wiley Online Library
This review surveys recent developments (reported in the last fifteen years) in
organometallic‐chemistry‐based methods for the functionalization of imidazo [1, 2‐a] …