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<p>hydrogen sulfide, giving the transient <a href="page.php?w=thioketone">thioketone</a> or <a href="page.php?w=thial">thial</a>, which typically convert to <a href="page.php?w=oligomer">oligomer</a>s.</p>

<p><big>1,2-Dithiols</big></p>
<p>Compounds containing thiol groups on adjacent carbon centers are common. <a href="page.php?w=Ethane-1%2C2-dithiol">Ethane-1,2-dithiol</a> reacts with aldehydes  and ketones  to give <a href="page.php?w=1%2C3-dithiolane">1,3-dithiolane</a>s:<br/>
:<chem>(HS)2C2H4 + R-CHO -> R-CHS2C2H4 + H2O</chem></p>

<p>Some dithiols</p><p>
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