摘要
<jats:title>Abstract</jats:title> <jats:p>The search for less time-consuming and inexpensive methods for the synthesis of disulfides continues to be a hot subject of research. Herein, we report that diisopropylamine (<jats:italic>i</jats:italic>Pr<jats:sub>2</jats:sub>NH) can act as a very effective catalyst for this process. The oxidative coupling of aryl thiols was carried out in the presence of catalytic amount of <jats:italic>i</jats:italic>Pr<jats:sub>2</jats:sub>NH in air (room temperature) in acetonitrile, without metal catalyst, additives, or external activators. This procedure opens a low-cost, green, and industrially applicable synthetic pathway to obtain aryl disulfides.</jats:p>
- 出版日期2018-2