Active Pd intermediates of the Suzuki-Miyaura reaction with low reactive aryl chlorides under “ligand-free” conditions
Author:
Funder
Russian Science Foundation
Irkutsk State University
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference41 articles.
1. An expedient, mild and aqueous method for Suzuki–Miyaura diversification of (hetero)aryl halides or (poly)chlorinated pharmaceuticals;Sharma;Org. Chem. Front.,2021
2. Palladium catalyzed C–C and C–N bond forming reactions: an update on the synthesis of pharmaceuticals from 2015 to 2020;Rayadurgam;Org. Chem. Front.,2021
3. Palladium-catalyzed coupling reactions in flavonoids: a retrospective of recent synthetic approaches;Ramos;Synth. Commun.,2021
4. Suzuki – Miyaura cross-coupling;Pagett,2020
5. The Suzuki-Miyaura reaction after the Nobel prize;Beletskaya;Coord. Chem. Rev.,2019
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1. Efficient heck and Suzuki-Miyaura cross-coupling reactions catalyzed by heterogeneous Pd NPs-decorated porous MOF catalysts under mild conditions;Journal of Molecular Structure;2024-08
2. Pd Single Atoms on N-Doped Hollow Carbon Nanosheet Assemblies for Suzuki Cross-Coupling Reactions of Aryl Chlorides;ACS Applied Nano Materials;2024-04-01
3. The role of phosphines in the activations of coupled substrates in the Suzuki—Miyaura reaction;Russian Chemical Bulletin;2024-03
4. Unveiling Pre-Transmetalation Intermediates in Base-Free Suzuki–Miyaura Cross-Couplings: A Computational Study;Inorganic Chemistry;2024-01-24
5. One-step Mo-doped praseodymium oxide construction of oxygen vacancies for efficient photothermal co-catalytic Suzuki coupling reaction;Molecular Catalysis;2024-01
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