Nickel and palladium catalysis: Stronger demand than ever

VM Chernyshev, VP Ananikov - Acs Catalysis, 2022 - ACS Publications
Key similarities and differences of Pd and Ni in catalytic systems are discussed. Overall, Ni
and Pd catalyze a vast number of similar C–C and C–heteroatom bond-forming reactions …

Mechanism and selectivity control in Ni-and Pd-catalyzed cross-couplings involving carbon–oxygen bond activation

SQ Zhang, X Hong - Accounts of Chemical Research, 2021 - ACS Publications
Conspectus Transition-metal-catalyzed C–O bond activation provides a useful strategy for
utilizing alcohol-and phenol-derived electrophiles in cross-coupling reactions, which has …

Selective C (aryl)–O bond cleavage in biorenewable phenolics

G De Smet, X Bai, BUW Maes - Chemical Society Reviews, 2024 - pubs.rsc.org
Biorefining of lignocellulosic biomass via a lignin first approach delivers a range of products
with high oxygen content. Besides pulp, a lignin oil rich in guaiacols and syringols is …

Selective C–O bond reduction and borylation of aryl ethers catalyzed by a rhodium–aluminum heterobimetallic complex

R Seki, N Hara, T Saito, Y Nakao - Journal of the American …, 2021 - ACS Publications
We report the catalytic reduction of a C–O bond and the borylation by a rhodium complex
bearing an X-type PAlP pincer ligand. We have revealed the reaction mechanism based on …

Broad-Scope Amination of Aryl Sulfamates Catalyzed by a Palladium Phosphine Complex

A Monti, J López-Serrano, A Prieto, MC Nicasio - ACS catalysis, 2023 - ACS Publications
Among phenol-derived electrophiles, aryl sulfamates are attractive substrates since they can
be employed as directing groups for C–H functionalization prior to catalysis. However, their …

Nickel‐Catalyzed Cross‐Electrophile Coupling of Aryl Phosphates with Aryl Bromides

JA Ren, X Chen, C Gui, C Miao, XQ Chu… - Advanced Synthesis …, 2023 - Wiley Online Library
A step‐economical and operationally simple nickel‐catalyzed cross‐electrophile coupling of
aryl phosphates with aryl bromides through C− O bond cleavage, which precluded the …

Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations of amide electrophiles

AS Bulger, DJ Nasrallah, AT Meza, NK Garg - Chemical Science, 2024 - pubs.rsc.org
Amide cross-couplings that rely on C–N bond activation by transition metal catalysts have
emerged as valuable synthetic tools. Despite numerous discoveries in this field, no catalytic …

Suzuki–Miyaura cross-coupling of esters by selective O–C (O) cleavage mediated by air-and moisture-stable [Pd (NHC)(μ-Cl) Cl] 2 precatalysts: catalyst evaluation …

S Yang, T Zhou, A Poater, L Cavallo… - Catalysis science & …, 2021 - pubs.rsc.org
The cross-coupling of aryl esters has emerged as a powerful platform for the
functionalization of otherwise inert acyl C–O bonds in chemical synthesis and catalysis …

Pd-catalyzed direct deoxygenative arylation of non-π-extended benzyl alcohols with boronic acids via transient formation of non-innocent isoureas

G Toupalas, G Thomann, L Schlemper… - ACS …, 2022 - ACS Publications
We report the direct arylation of non-derivatized alcohols with boronic acids and
demonstrate that a Pd catalyst, in combination with a carbodiimide, can be used to forge a C …

Buchwald–Hartwig Amination and C–S/S–H Metathesis of Aryl Sulfides by Selective C–S Cleavage Mediated by Air- and Moisture-Stable [Pd(NHC)(μ-Cl)Cl]2 …

S Yang, X Yu, A Poater, L Cavallo, CSJ Cazin… - Organic …, 2022 - ACS Publications
We report a combined experimental and mechanistic study on the Buchwald–Hartwig
amination and C–S/S–H metathesis of aryl sulfides by selective activation of C–S bonds …