RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, D-52074 Aachen, Germany.
Chem Commun (Camb). 2019 Jan 2;55(3):338-341. doi: 10.1039/c8cc08821g.
Sulfur ylides are well-known to undergo sigmatropic rearrangement reaction. Herein, we describe a novel reactivity of sulfur ylides, which provides access to the product of a formal functional group metathesis upon dealkylative interception of the rearrangement process. Using a simple iron catalyst and in situ generated diazoalkanes this method provides access to α-mercaptoacetonitrile derivatives.
硫叶立德是众所周知的经历[sigma]重排反应。在此,我们描述了硫叶立德的一种新的反应性,它提供了一种在重排过程中脱烷基捕获后得到的官能团变换反应产物的方法。使用简单的铁催化剂和原位生成的重氮烷烃,该方法可用于合成α-巯基乙腈衍生物。