Some stilbene ozonides react mith dimethyl THE recent report1 that ozonides are readily solvolysed by sulphoxide, dimethyfformamide, and primary, secondary alcohols prompts us to report our observations on the and tertiary amines to give a single aldehyde and a reactions of some stilbene ozonides with dimethyl sulphsingle acid in quantitative yield oxide, dimethylformamide, and amines The ozonides
a-Alkoxybenzyl hydroperoxides are converted rapidly and quantitatively a t room temperature into the corresponding alkyl benzoates by primary, secondary, and tertiary amines and by dimethyl sulphoxide.
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