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Electrochemical Oxidation of Diols Mediated by Organotin Compounds

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Book cover Novel Trends in Electroorganic Synthesis

Abstract

A new diol selective electrochemical oxidation method has been developed utilzing dibutyltin oxide and bromide anion as mediators. The oxidation proceeded effectively at 0°C under nutral condition. Cyclohexane diol was selectivly oxidized even in the presence of excess primary or secondary alcohols.

Determined by GLC.

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Reference

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© 1998 Springer Japan

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Maki, T., Fukae, K., Harasawa, H., Ohishi, T., Matsumura, Y. (1998). Electrochemical Oxidation of Diols Mediated by Organotin Compounds. In: Torii, S. (eds) Novel Trends in Electroorganic Synthesis. Springer, Tokyo. https://doi.org/10.1007/978-4-431-65924-2_40

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  • DOI: https://doi.org/10.1007/978-4-431-65924-2_40

  • Publisher Name: Springer, Tokyo

  • Print ISBN: 978-4-431-65926-6

  • Online ISBN: 978-4-431-65924-2

  • eBook Packages: Springer Book Archive

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