Copper(II) Tetrafluoroborate Catalyzed Ring-Opening Reaction of Epoxides with Alcohols at Room Temperature
Organic Letters2002Vol. 4(17), pp. 2817–2819
Citations Over TimeTop 10% of 2002 papers
Abstract
[reaction: see text] Efficient ring opening of different epoxides by reaction with representative alcohols is presented. These processes were carried out at room temperature and rely on the usefulness of commercial copper tetrafluoroborate as catalyst.
Related Papers
- → Densities and viscosities for ionic liquids mixtures containing [eOHmim][BF4], [bmim][BF4] and [bpy][BF4](2014)64 cited
- → Synthesis and Characterization of Pyrylogens Possessing Low Excitation Energies – Substituent Modification in Order to Improve Solar Energy Collection(2012)7 cited
- → Polygold(1-adamantyl)ammonium Salts(1997)7 cited
- → Improved Preparation of 1,3-Bis(2,6-di-iso-propylphenyl)imidazolium Tetrafluoroborate(2013)2 cited
- → Electrochemical Reduction of Cobalt Tetrafluoroborate in 1‐Butyl‐3‐Methylimidazolium Tetrafluoroborate Ionic Liquid(2015)1 cited