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Journal of Lipid Research, Vol. 9, 137-139, January 1968
Copyright © 1968 by Lipid Research, Inc.
Department of Physiological Chemistry, The Ohio State University, Columbus, Ohio 43210
Unsaturated methyl esters were cleaved to aldehydes and aldehydo-esters by ozonolysis followed by reduction with dimethyl sulfide after conversion to hydroperoxides. Cleavage products were identified by thin-layer chromatography and quantified by temperature programmed gas-liquid chromatography.
Supplementary key words ozonolysis-reduction unsaturated methyl esters ozonides hydroperoxides aldehydes aldehydo-esters dimethyl sulfide dimethyl sulfoxide thin-layer chromatography gas-liquid chromatography
Submitted on August 28, 1967
Accepted on October 9, 1967
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