Pyreneacyl sulfides as a visible light-induced versatile ligation platform

Chem Commun (Camb). 2017 Apr 18;53(32):4501-4504. doi: 10.1039/c7cc00711f.

Abstract

We report a visible light responsive moiety capable of generating highly reactive thioaldehydes. Upon irradiation with visible light (420 nm) the pyreneacyl sulfide species undergoes a Norrish II elimination yielding thioaldehydes capable of being trapped by nucleophiles (amines, aminoxys, and thiols), as well as Diels-Alder processes, representing a new versatile ligation platform.