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    • https://espanol.libretexts.org/Quimica/Libro%3A_Qu%C3%ADmica_Org%C3%A1nica_con_%C3%A9nfasis_Biol%C3%B3gico_(Soderberg)/11%3A_Reacciones_de_adicion_nucleofilica_de_carbonilo/11.7%3A_Formaci%C3%B3n_de_Imina_(base_de_Schiff)
      Based on your knowledge of the mechanism of acetal and ketal formation, you might expect that the next step would be attack by a second amine to form a compound with a carbon bound to two amine groups...Based on your knowledge of the mechanism of acetal and ketal formation, you might expect that the next step would be attack by a second amine to form a compound with a carbon bound to two amine groups – the nitrogen version of a ketal. A key step in this process is the formation of a Schiff base between one of the reactants and a lysine in the active site of the enzyme.

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