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Abstract Preparation of barium manganate in large-scale is discussed. It is also shown that this reagent is capable of oxidizing organic substrates, converting alcohols to their corresponding carbonyl compounds, aromatic amines to their corresponding azo compounds, hydroquinone to p-benzoquinone, benzylamine to benzaldehyde, and triphenylphosphine to its oxide in good yields. Saturated hydrocarbons, unsaturated hydrocarbons, unsaturated ketones, and saturated amines are not affected by this reagent in a reasonable reaction time.
Firouzabadi et al. (Tue,) studied this question.
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