Allylic Ethers as Educts for Suzuki−Miyaura Couplings in Water at Room Temperature
- 11 August 2009
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 131 (34), 12103-12105
- https://doi.org/10.1021/ja905082c
Abstract
The first examples of Suzuki−Miyaura couplings of allylic ethers are reported. These can be done not only under very mild room-temperature conditions but also in water as the only medium. The process is made possible by micellar catalysis using the designer surfactant PTS.This publication has 49 references indexed in Scilit:
- The Development of Versatile Methods for Palladium-Catalyzed Coupling Reactions of Aryl Electrophiles through the Use of P(t-Bu)3 and PCy3 as LigandsAccounts of Chemical Research, 2008
- Room-Temperature Palladium-Catalyzed Allyl Cross-Coupling Reaction with Boronic Acids Using Phosphine-Free Hydrazone LigandsSynlett, 2008
- Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine LigandsAccounts of Chemical Research, 2008
- Microwave-assisted arylation of rac-(E)-3-acetoxy-1,3-diphenylprop-1-ene with arylboronic acidsTetrahedron, 2007
- Microwave-Enhanced Palladium-Catalyzed Cross-Coupling Reactions of Potassium Vinyltrifluoroborates and Allyl Acetates: A New Route to 1,4-PentadienesOrganic Letters, 2005
- Suzuki–Miyaura and Related Cross‐Couplings in Aqueous Solvents Catalyzed by Di(2‐pyridyl)methylamine‐Palladium Dichloride ComplexesAdvanced Synthesis & Catalysis, 2004
- Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesisTetrahedron, 2002
- A Novel Palladium Catalyst for Cross-Coupling of Allyl Acetates with Arylboronic AcidsEuropean Journal of Organic Chemistry, 2002
- Nickel(0)-catalyzed asymmetric cross-coupling reactions of allylic compounds with arylboronic acidsJournal of the Chemical Society, Perkin Transactions 1, 2000
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995