be used as a versatile reagent in organic synthesis. Primary and secondary alcohols are converted to their carbonyl compounds, α-hydroxy ketones to their diketones, and hydroquinones to their quinones. Aromatic amines are converted to their azo compounds, benzylamine to benzaldehyde, phenylhydrazones and oximes to their carbonyl compounds. Thiols are also converted to their disulfides in high yields
Barium Manganate. A Versatile Oxidant in Organic Synthesis
作者:Habib Firouzabadi、Zohreh Mostafavipoor
DOI:10.1246/bcsj.56.914
日期:1983.3
shown that this reagent is capable of oxidizing organic substrates, converting alcohols to their corresponding carbonyl compounds, aromaticamines 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