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The hydroperoxides in oxidised methyl oleate can be converted in high yield into the dinitro‐phenylhydrazones of aldehydes and aldehyde esters by reaction on a Celite/dinitrophenylhydrazine‐hydrochloric acid column. The aldehydes and aldehyde esters formed are the same as those produced during the thermal decomposition of methyl oleate hydroperoxide. The dinitrophenylhydrazones of unsaturated conjugated C 18 keto esters are also formed.
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M. M. Horikx (1964) studied this question.
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