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Electroepoxidation of natural and synthetic alkenes mediated by sodium bromide

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2009 Inês CRC.pdf316.71 KBAdobe PDF Download

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Abstract(s)

Electroepoxidation of synthetic alkenes (styrene, trans-stilbene and trans-b-methylstyrene) and of some natural terpenes (limonene, terpinolene, geraniol, a-terpinene, g-terpinene and a-terpineol) mediated by sodium bromide was performed in MeCN:H2O (4:1) at platinum electrodes. The indirect electrochemical oxidation of the olefins led to the corresponding epoxides in yields ranging from 23% to 79%.

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Electrochemical epoxidation Sodium bromide Alkenes Terpenes

Citation

Inês, M., Mendonça, A. J., Esteves, A. P., Mendonça, D. I., & Medeiros, M. J. (2009). Electroepoxidation of natural and synthetic alkenes mediated by sodium bromide. Comptes Rendus Chimie, 12(8), 841-849. doi:10.1016/j.crci.2008.10.014

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