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 …

Conducting polymers for optoelectronic devices and organic solar cells: A review

A R. Murad, A Iraqi, SB Aziz, S N. Abdullah, MA Brza - Polymers, 2020 - mdpi.com
In this review paper, we present a comprehensive summary of the different organic solar cell
(OSC) families. Pure and doped conjugated polymers are described. The band structure …

Solvent effects in palladium catalysed cross-coupling reactions

J Sherwood, JH Clark, IJS Fairlamb, JM Slattery - Green Chemistry, 2019 - pubs.rsc.org
Palladium catalysed cross-couplings reactions have been a dominant method in synthetic
chemistry for decades. Despite this, the role of the solvent is often taken for granted and …

Selection of boron reagents for Suzuki–Miyaura coupling

AJJ Lennox, GC Lloyd-Jones - Chemical Society Reviews, 2014 - pubs.rsc.org
Suzuki–Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal
catalysed carbon–carbon bond forming reaction to date. Its success originates from a …

Computational studies of synthetically relevant homogeneous organometallic catalysis involving Ni, Pd, Ir, and Rh: an overview of commonly employed DFT methods …

T Sperger, IA Sanhueza, I Kalvet… - Chemical …, 2015 - ACS Publications
The field of organometallic catalysis has attracted considerable interest from both academia
and industry due to its broad applications in synthetic transformations. Pd, Ni, Rh, and Ir …

Palladium-catalyzed Suzuki− Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands

R Martin, SL Buchwald - Accounts of chemical research, 2008 - ACS Publications
The cores of many types of polymers, ligands, natural products, and pharmaceuticals
contain biaryl or substituted aromatic structures, and efficient methods of synthesizing these …

Transmetalation in the Suzuki–Miyaura coupling: the fork in the trail

AJJ Lennox, GC Lloyd‐Jones - … Chemie International Edition, 2013 - Wiley Online Library
Abstract The Suzuki–Miyaura coupling is one of the few transition‐metal‐catalyzed C C
bond‐forming reactions that have been used in applications ranging from discovery …

Distinguishing between pathways for transmetalation in Suzuki− Miyaura reactions

BP Carrow, JF Hartwig - Journal of the American Chemical …, 2011 - ACS Publications
We report a systematic study of the stoichiometric reactions of isolated arylpalladium
hydroxo and halide complexes with arylboronic acids and aryltrihydroxyborates to evaluate …

Computational perspective on Pd-catalyzed C–C cross-coupling reaction mechanisms

M Garcia-Melchor, AAC Braga, A Lledos… - Accounts of chemical …, 2013 - ACS Publications
Palladium-catalyzed C–C cross-coupling reactions (Suzuki–Miyaura, Negishi, Stille,
Sonogashira, etc.) are among the most useful reactions in modern organic synthesis …

Synthesis of axially chiral biaryl compounds by asymmetric catalytic reactions with transition metals

P Loxq, E Manoury, R Poli, E Deydier… - Coordination Chemistry …, 2016 - Elsevier
Axially chiral biaryl structures are unique systems encountered in various synthetic
compounds such as BINAP and BINOL, polymers, but also in natural products presenting a …