Computational mechanistic analysis of a cationic Suzuki–Miyaura reaction without added base
Author:
Affiliation:
1. Division of Quantum Chemistry and Department of Chemistry, KU Leuven, Celestjjnenlaan 200F, B-3001 Leuven, Belgium
Abstract
Publisher
Royal Society of Chemistry (RSC)
Subject
Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2023/CY/D2CY01780F
Reference39 articles.
1. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
2. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
3. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
4. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
5. A Rationally Designed Universal Catalyst for Suzuki–Miyaura Coupling Processes
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Comparative analysis of palladium, nickel and copper phosphane/carbene catalysts in Suzuki–Miyaura couplings: Mechanistic insights and reactivity trends;Advances in Inorganic Chemistry;2024
2. Heteroaryl–Heteroaryl Suzuki–Miyaura Cross-Coupling Enabled by Large-but-Flexible Dibenzobarrelene-Derived Pd-NHC Precatalysts;Organometallics;2023-07-25
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