Direct Conversion of Silyl Ethers Into Carbonyl Compounds with Jones Reagent in the Presence of Potassium Fluoride
- 1 July 1985
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 15 (9) , 759-764
- https://doi.org/10.1080/00397918508063869
Abstract
Treatment of silyl ethers with Jones reagent in acetone in the presence of potassium fluoride resulted in the silicon-oxygen bond cleavage and oxidation to give carbonyl compounds directly.Keywords
This publication has 5 references indexed in Scilit:
- Alkyl silyl ethersPublished by Elsevier ,1981
- Synthetic Methods and Reactions; 951. Ceric Ammonium Nitrate-Catalyzed Oxidative Cleavage of Alkyl and Silyl Ethers with Sodium BromateSynthesis, 1980
- The Preparation and Synthetic Utility of tert-Butyldiphenylsilyl EthersCanadian Journal of Chemistry, 1975
- Notes - The Direct Conversion of Steroidal Δ5-3β-Alcohols to Δ5- and Δ4-3-KetonesThe Journal of Organic Chemistry, 1956
- 13. Researches on acetylenic compounds. Part I. The preparation of acetylenic ketones by oxidation of acetylenic carbinols and glycolsJournal of the Chemical Society, 1946