Palladium-Catalyzed Saegusa–Ito Oxidation: Synthesis of α, β-Unsaturated Carbonyl Compounds from Trimethylsilyl Enol Ethers
…, PL Nguyen, N Lévaray, H Lebel
Index: Lu, Yingdong; Nguyen, Pierre Long; Levaray, Nicolas; Lebel, Heleine Journal of Organic Chemistry, 2013 , vol. 78, # 2 p. 776 - 779
Full Text: HTML
Citation Number: 15
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 Articles:
[Kerr, William J.; Pearson, Colin M.; Thurston, Graeme J. Organic and Biomolecular Chemistry, 2006 , vol. 4, # 1 p. 47 - 50]
[Nicolaou; Gray, David L. F.; Montagnon, Tamsyn; Harrison, Scott T. Angewandte Chemie - International Edition, 2002 , vol. 41, # 6 p. 996 - 1000]
[Nicolaou; Gray, David L. F.; Montagnon, Tamsyn; Harrison, Scott T. Angewandte Chemie - International Edition, 2002 , vol. 41, # 6 p. 996 - 1000]
[Kyte, Brian G.; Rouviere, Pierre; Cheng, Qiong; Stewart, Jon D. Journal of Organic Chemistry, 2004 , vol. 69, # 1 p. 12 - 17]
[Coote, Susannah C.; O'Brien, Peter; Whitwood, Adrian C. Organic and Biomolecular Chemistry, 2008 , vol. 6, # 23 p. 4299 - 4314]