Synthesis of Arylpalladium(II) Boronates: Confirming the Structure and Chemical Competence of Pre‐transmetalation Intermediates in the Suzuki–Miyaura Reaction
Author:
Affiliation:
1. School of Natural Sciences—Chemistry University of Tasmania Hobart Tasmania Australia
2. Department of Chemistry University of Otago Dunedin, Otago New Zealand
3. Central Science Laboratory University of Tasmania Hobart Tasmania Australia
Funder
Australian Research Council
Publisher
Wiley
Subject
General Chemistry,Catalysis
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202104802
Reference27 articles.
1. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
3. Selection of boron reagents for Suzuki–Miyaura coupling
4. Enantiospecific and Iterative Suzuki–Miyaura Cross-Couplings
5. Carbon–carbon bonding made easy
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4. Pyrazine Derivative as Supramolecular Host for Immobilization of Palladium Nanoparticles for Efficient Suzuki Coupling;European Journal of Organic Chemistry;2023-07-14
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