Pyreneacyl sulfides as a visible light-induced versatile ligation platform†
Chemical Communications Pub Date : 03/28/2017 00:00:00 , 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.

Graphical abstract: Pyreneacyl sulfides as a visible light-induced versatile ligation platform