A NEW METHOD FOR DIRECT OXIDATION OF THE METHYLENE GROUP ADJACENT TO A CYCLOPROPANE RING TO THE KETO GROUP
- 5 September 1985
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 14 (9) , 1385-1386
- https://doi.org/10.1246/cl.1985.1385
Abstract
A new finding that the methylene group adjacent to a cyclopropane ring can be oxidized to the keto group directly with ruthenium tetroxide is described.This publication has 7 references indexed in Scilit:
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- Stereochemical Studies on the Nucleophilic Substitution in the Reaction of Allylic Phosphates with Organoaluminum ReagentsBulletin of the Chemical Society of Japan, 1980
- Oxidation of Cyclopropyl Hydrocarbons with OzoneAngewandte Chemie International Edition in English, 1976
- Oxidation of hydrocarbons. VI. Oxidation of cycloalkanes by ruthenium tetroxideThe Journal of Organic Chemistry, 1975
- Dry ozonation. Method for stereoselective hydroxylation of saturated compounds on silica gelThe Journal of Organic Chemistry, 1975
- Procedure for the methylenation of olefins to cyclopropanesThe Journal of Organic Chemistry, 1970
- Cyclopropane rings as proton-acceptor groups in hydrogen bondingJournal of the American Chemical Society, 1968