Research demonstrates reduction of cyclooctene ozonolysis peroxides using sebacic acid dihydrazide, suggesting new synthetic routes.
It was found that the reduction of ozonolysis peroxide of cyclooctene products by sebacic acid dihydrazide in solvents of various natures leads to the formation of three acyclic differently functionalized cyclooctene derivatives: in methanol - dimethyl 11,20-dioxo-9,10,21,22-tetraazatriacont-8E,22E-dienoic acid, in methylene chloride - 11,20-dioxo-9,10,21,22-tetraazatriacta-8E,22E-diene acid, in THF - natural cortic acid.
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M. P. Yakovleva (2025) studied this question.
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