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 …

Transition metal (Ni, Cu, Pd)-catalyzed alkene dicarbofunctionalization reactions

LM Wickham, R Giri - Accounts of chemical research, 2021 - ACS Publications
Conspectus Recently, alkene dicarbofunctionalization, ie, the powerful organic synthesis
method of alkene difunctionalization with two carbon sources, emerged as a formidable …

Recent development of aryl diazonium chemistry for the derivatization of aromatic compounds

F Mo, D Qiu, L Zhang, J Wang - Chemical Reviews, 2021 - ACS Publications
Aryl diazonium salts are versatile building blocks in organic synthesis. In light of the ever-
increasing importance of aryl diazonium salts spanning most disciplines of the chemical …

The Suzuki-Miyaura reaction after the Nobel prize

IP Beletskaya, F Alonso, V Tyurin - Coordination Chemistry Reviews, 2019 - Elsevier
Synthetic organic chemistry experienced a significant advance in the last quarter of the 20th
century with the advent of the transition-metal catalyzed cross-coupling reactions. The utility …

Base-free nickel-catalysed decarbonylative Suzuki–Miyaura coupling of acid fluorides

CA Malapit, JR Bour, CE Brigham, MS Sanford - Nature, 2018 - nature.com
Abstract The Suzuki–Miyaura cross-coupling of organoboron nucleophiles with aryl halide
electrophiles is one of the most widely used carbon–carbon bond-forming reactions in …

Visible‐Light‐Induced Selective Defluoroborylation of Polyfluoroarenes, gem‐Difluoroalkenes, and Trifluoromethylalkenes

W Xu, H Jiang, J Leng, HW Ong, J Wu - Angewandte Chemie, 2020 - Wiley Online Library
Fluorinated organoboranes serve as versatile synthetic precursors for the preparation of
value‐added fluorinated organic compounds. Recent progress has been mainly focused on …

Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions

FX Felpin, S Sengupta - Chemical Society Reviews, 2019 - pubs.rsc.org
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …

Deaminative reductive arylation enabled by nickel/photoredox dual catalysis

J Yi, SO Badir, LM Kammer, M Ribagorda… - Organic …, 2019 - ACS Publications
Described is a cross-electrophilic, deaminative coupling strategy harnessing Katritzky salts
as a new species of electrophile in Ni/photoredox dual catalytic reductive cross-coupling …

Ylide-substituted phosphines: A platform of strong donor ligands for gold catalysis and palladium-catalyzed coupling reactions

S Lapointe, A Sarbajna… - Accounts of Chemical …, 2022 - ACS Publications
Conspectus The development of homogeneous catalysts is strongly connected to the design
of new, sophisticated ligands, which resolve limitations of a given reaction protocol by …

Gold-catalyzed chemoselective couplings of polyfluoroarenes with aryl germanes and downstream diversification

A Dahiya, C Fricke, F Schoenebeck - Journal of the American …, 2020 - ACS Publications
This report describes the chemoselective coupling of polyfluoroarenes with aryl germanes in
the presence of aromatic C–I, C–Br, C–Cl, C–OTf, and C–SiMe3 groups, as well as …