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<strong>Sintesi</strong> <strong>di</strong> <strong>Ammine</strong>1. Alchilazione <strong>di</strong>retta per l’ottenimento <strong>di</strong> ammine 1°2. <strong>Sintesi</strong> <strong>di</strong> Gabriel <strong>di</strong> ammine 1°3. Riduzione:– <strong>di</strong> azi<strong>di</strong>– <strong>di</strong> nitrili– <strong>di</strong> ammi<strong>di</strong>– <strong>di</strong> ossime4. Aminazione riduttiva <strong>di</strong> aldei<strong>di</strong> o chetoni5. Riduzione <strong>di</strong> nitrocomposti aromatici6. Riarrangiamento <strong>di</strong> Hofmann7. Riarrangiamento <strong>di</strong> Curtius12
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