A Mild Oxidation of Aromatic Amines

DOI: 10.1016/0040-4039(95)00281-G

Source and publish data:

Tetrahedron Letters p. 2377 - 2378 (1995)

Update date:2022-08-16

Topics:

Authors:

Webb, Kevin S.

Seneviratne, Viran

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Article abstract of DOI:10.1016/0040-4039(95)00281-G

Several primary aromatic amines have been converted to the corresponding nitro compounds in good yields.The oxidant was oxone (potassium peroxymonosulfate) and the reactions were performed in 5 to 20percent aqueous acetone and buffered with sodium bicarbonate.

Full text of DOI:10.1016/0040-4039(95)00281-G

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