Palladium-Catalyzed Saegusa–Ito Oxidation: Synthesis of α,β-Unsaturated Carbonyl Compounds from Trimethylsilyl Enol Ethers
The Journal of Organic Chemistry2012Vol. 78(2), pp. 776–779
Citations Over TimeTop 15% of 2012 papers
Abstract
Palladium-catalyzed Saegusa-Ito oxidation of trimethylsilyl enol ethers is possible using Oxone as a stoichiometric oxidant and sodium hydrogen phosphate as a buffer. Cyclic and acyclic enones as well as α,β-unsaturated aldehydes are obtained in good to excellent yields.
Related Papers
- → Preparation of organo palladium sols from palladium complexes in various alcohols(1994)32 cited
- → The constitution of cerium-palladium alloys containing 50–100% palladium(1967)48 cited
- → Allyl(β‐diketonato)palladium(II) complexes as precursors for palladium films(1994)36 cited
- → Reduction of palladium(II) monoglycinate complexes at rotating disc palladium electrode in acid media(2010)1 cited
- Rapid Determination of Palladium in Palladium-Nickel and Palladium-Cobalt Plating Bath(2003)