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<p><big>Reaction mechanism</big></p>
<p>The mechanism of the Mannich reaction starts with the formation of an <a href="page.php?w=iminium">iminium</a> ion from the amine and aldehyde.The compound with the carbonyl functional group (in this case a <a href="page.php?w=ketone">ketone</a>) will <a href="page.php?w=keto-enol_tautomerism">tautomerize</a> to the enol form, after which it attacks the iminium ion.</p>

<p><big>Asymmetric Mannich reactions</big></p>
<p>If the enolizable ketone or aldehyde has a substituent at the ?-position, proline and similar-amino acid</p><p>
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