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Naphthyridinones and the Like

8-Naphthyridinones are usually tautomeric with corresponding naphthyridi-nols, but they may be fixed (become nontautomeric) by /V-alkylation. As in related series, 1,8-naphthyridinones prefer to exist as oxo rather than hydroxy [Pg.221]

The mass spectra of such naphthyridinones have been studied.286 [Pg.221]


See other pages where Naphthyridinones and the Like is mentioned: [Pg.44]    [Pg.46]    [Pg.116]    [Pg.118]    [Pg.221]    [Pg.221]    [Pg.223]    [Pg.224]    [Pg.225]    [Pg.44]    [Pg.46]    [Pg.116]    [Pg.118]    [Pg.221]    [Pg.221]    [Pg.223]    [Pg.224]    [Pg.225]    [Pg.259]    [Pg.266]   


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Naphthyridinones

Preparation of 1,6-Naphthyridinones and the Like

Preparation of Tautomeric 1,5-Naphthyridinones and the Like

Reactions of 1,6-Naphthyridinones and the Like

Reactions of Tautomeric 1,5-Naphthyridinones and the Like

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