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1984•Journal of the Chemical Society Perkin Transactions 1Requires access

Stereochemistry of olefin and fatty acid oxidation. Part 3. The allylic hydroperoxides from the autoxidation of methyl oleate

E. N. Frankel, R. F. Garwood, Bhupinder P. S. Khambay, Gerard P. Moss, B. C. L. Weedon

Open publisher page 55 citations

Abstract

Methods have been developed, using 13C n.m.r. spectroscopy and mass spectrometry, for the analysis of all eight cis and trans allylic 8-, 9-, 10-, and 11-hydroperoxides formed on autoxidation of methyl oleate.

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Methods have been developed, using 13C n.m.r. spectroscopy and mass spectrometry, for the analysis of all eight cis and trans allylic 8-, 9-, 10-, and 11-hydroperoxides formed on autoxidation of methyl oleate.

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OpenAlex reports 55 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Methods have been developed, using 13C n.m.r. spectroscopy and mass spectrometry, for the analysis of all eight cis and trans allylic 8-, 9-, 10-, and 11-hydroperoxides formed on autoxidation of methyl oleate.

Key concepts: Autoxidation, Allylic rearrangement, Chemistry, Methyl oleate, Mass spectrometry, Olefin fiber, Organic chemistry, Fatty acid

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