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<p><a href="page.php?w=cyclopentanone">cyclopentanone</a>. <a href="page.php?w=Acid_anhydride">Acid anhydride</a>s and some <a href="page.php?w=lactone">lactone</a>s also give thioesters upon treatment with thiols in the presence of a base.</p>

<p>Thioesters can be conveniently prepared from alcohols by the <a href="page.php?w=Mitsunobu_reaction">Mitsunobu reaction</a>, using <a href="page.php?w=thioacetic_acid">thioacetic acid</a>.</p>

<p>They also arise via <a href="page.php?w=carbonylation">carbonylation</a> of <a href="page.php?w=alkyne">alkyne</a>s</p><p>
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