Liquid-phase synthesis of cyclic diene diepoxides using metal halides and hydrogen peroxide

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Abstract

Optimal conditions were found for induced hydroxyhalogenation of cyclic dienes (tetrahydroindene, 4-vinylcyclohexene and 5-vinyl- and 5-cyclohexenylbicyclo[2.2.1]hept-2-enes) in the system [MHlg-HA or HHlg]-H 2O2 (or NaClO). Dehydrohalogenation of the chloro- and bromohydrins thus obtained with powdered potassium carbonate gave the corresponding diepoxy derivatives, and their hydrolysis led to mixtures of stereoisomeric tetrahydric alcohols. © Pleiades Publishing, Ltd., 2012.

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Alimardanov, K. M., Sadygov, O. A., Garibov, N. I., & Abdullaeva, M. Y. (2012). Liquid-phase synthesis of cyclic diene diepoxides using metal halides and hydrogen peroxide. Russian Journal of Organic Chemistry, 48(10), 1302–1308. https://doi.org/10.1134/S1070428012100077

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