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Benzo quinoxalines table

The pyrazine ring is relatively stable to oxidation, and many pyrazine-carboxylic acids have been prepared from quinoxalines, phenazines, and other fused pyrazines by oxidation with potassium permanganate. This reaction has been most used for the oxidation of quinoxalines, for example, 77 -> 78. The oxidations are usually carried out with potassium permanganate in alkali (397), but may also be effected without added base (398). Crippa and Perroncito (399) have also used chromic oxide in acetic acid-acetic anhydride to oxidize benzo(/]quinoxalines (79). Pyrazines prepared by this method are summarized in Table 11.9 (397-419). [Pg.37]


See other pages where Benzo quinoxalines table is mentioned: [Pg.712]    [Pg.723]    [Pg.73]    [Pg.730]    [Pg.730]    [Pg.736]    [Pg.739]    [Pg.224]   
See also in sourсe #XX -- [ Pg.723 , Pg.739 ]




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Benzo quinoxaline

Benzo quinoxalines

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