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Oxidation of alcohols by active species generated by electrochemical oxidation of organosulfur compounds

✍ Scribed by Tatsuya Shono; Yoshihiro Matsumura; Mikiko Mizoguchi; Jue Hayashi

Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
159 KB
Volume
20
Category
Article
ISSN
0040-4039

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✦ Synopsis

Oxidation of secondary alcohols to ketones was accomplished by an indirect electrochemical method utilizing thioanisole as a catalytic electron carrier.

πŸ“œ SIMILAR VOLUMES

Aromatic iodination by positive iodine a
Aromatic iodination by positive iodine active species generated by anodic oxidation in trimethyl orthoformate
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✍ Johannes Kaulen; Hans-J. SchΓ€fer πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 979 KB

Primary alcohols, ol,w-diols and secondary alcohols are easily transformed into carboxylic acids, dicarboxylic acids or ketones, respectively, by heterogeneous oxidation with nickel oxide hydroxide electrochemicahy regenerated at a nickel hydroxyde electrode. The results are discussed in comparison