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Sodium arsenate nitro compounds

An interesting reduction of aromatic nitro compounds which uses glucose in an alkaline medium (equation 7) has received little attention. The advantages of this reaction include high yields, rapid rate and ease of product isolation from oxidation by-products. Other reagents which bring about the reduction of nitroanenes to azoxy compounds include potassium borohydride, sodium arsenate, phosphine and yellow phosphorus. Electrolytic methods have also been utilized. ... [Pg.366]

See other pages where Sodium arsenate nitro compounds is mentioned: [Pg.44]    [Pg.44]    [Pg.233]    [Pg.264]    [Pg.1481]    [Pg.1481]    [Pg.195]    [Pg.428]    [Pg.264]    [Pg.950]    [Pg.1069]    [Pg.1070]    [Pg.415]   
See also in sourсe #XX -- [ Pg.366 ]

See also in sourсe #XX -- [ Pg.8 , Pg.366 ]

See also in sourсe #XX -- [ Pg.8 , Pg.366 ]



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