Dealkylative intercepted rearrangement reactions of sulfur ylides

Chem Commun (Camb). 2019 Jan 2;55(3):338-341. doi: 10.1039/c8cc08821g.

Abstract

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.