THE OXIDATION OF ALCOHOLS TO CARBONYL COMPOUNDS VIA ALKOXYMAGNESIUM BROMIDES
- 5 July 1975
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 4 (7) , 691-694
- https://doi.org/10.1246/cl.1975.691
Abstract
Alkoxymagnesium bromides prepared from alcohols and ethylmagnesium bromide are oxidized with N-chlorosuccinimide in the presence of lithium tert-butoxide to afford the corresponding carbonyl compounds in good yields.Keywords
This publication has 6 references indexed in Scilit:
- Sullfoxonium salts as reagents for oxidation of primary and secondary alcohols to carbonyl compoundsThe Journal of Organic Chemistry, 1974
- Improved sythetic routes to prostaglandins utilizing sulfide-mediated oxidation of primary and secondary alcoholsThe Journal of Organic Chemistry, 1973
- New and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compoundsJournal of the American Chemical Society, 1972
- Dimethyl Sulfoxide OxidationsChemical Reviews, 1967
- Sulfoxide-Carbodiimide Reactions. I. A Facile Oxidation of AlcoholsJournal of the American Chemical Society, 1965
- Oxidations and Dehydrogenations with N-Bromosuccinimide and Related N-Haloimides.Chemical Reviews, 1963