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June 1, 1993Bulletin of the Chemical Society of Japan

Potassium Permanganate Oxidation of Ketone Oximes. A Deprotective Version

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Abstract

KMnO4 in acetonitrile–water has been found to be a convenient system for regenerating ketones from ketone oximes under mild conditions.

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Cite This Study

Wali et al. (1993) studied this question.

synapsesocial.com/papers/6a910cc255de849fda7a7a65 https://doi.org/10.1246/bcsj.66.1847

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Oxidative Cleavage of Ketoximes with Iodosobenzene DiacetateOriginal Research · 1986 · 39 citations
2Levulinic Acid as a Reagent for the Hydrolysis of Oximes and 2,4-DinitrophenylhydrazonesOriginal Research · 1959 · 103 citations
3An Effective General Method for Oxidizing Salts of Mononitro Compounds with Neutral Permanganate to Aldehydes and Ketones1aOriginal Research · 1962 · 71 citations
4A simple, efficient, and highly selective method for the regeneration of carbonyl compounds from oximes and semicarbazonesOriginal Research · 1988 · 67 citations
5Thallium in organic synthesis. XXVI. Direct conversion of oximes into aldehydes and ketones with thallium(III) nitrate (TTN)Original Research · 1971 · 71 citations