Aryl Trifluoroborates in Suzuki-Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and Fluoride
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis
Reference79 articles.
1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
2. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
3. Suzuki–Miyaura Cross‐Coupling Reactions of Alkylboronic Acid Derivatives or Alkyltrifluoroborates with Aryl, Alkenyl or Alkyl Halides and Triflates
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1. A New Discovery on the Potential Stability of Ion-Selective Membranes: The Poison from Tetrahydrofuran;ACS Sensors;2024-08-08
2. Phase transfer catalysts shift the pathway to transmetalation in biphasic Suzuki-Miyaura cross-couplings;Nature Communications;2024-06-27
3. A Simple Device for Automated Mixing of Heterogeneous Solid‐Liquid Reactions During In‐Situ Monitoring by NMR Spectroscopy;European Journal of Organic Chemistry;2024-04-09
4. Rapid, Homogenous, B-Alkyl Suzuki–Miyaura Cross-Coupling of Boronic Esters;The Journal of Organic Chemistry;2024-03-14
5. Anhydrous and Stereoretentive Fluoride-Enhanced Suzuki–Miyaura Coupling of Immunomodulatory Imide Drug Derivatives;The Journal of Organic Chemistry;2024-03-07
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