Direct annulation between glycine derivatives and thiiranes through photoredox/iron cooperative catalysis

A visible-light-induced aerobic oxidative [2+3] cycloaddition reaction between glycine derivatives and thiiranes has been disclosed, which provides an efficient and atom-economical strategy for the rapid synthesis of thiazolidine-2-carboxylic acid derivatives and the post-modification of glycine-derived dipeptides under mild conditions with good yield and high diastereoselectivities. A preliminary mechanistic study favors a pathway involving a cooperative photoredox catalysis and iron catalysis. A visible-light-induced aerobic oxidative [2+3] cycloaddition reaction between glycine derivatives and thiiranes is achieved via a cooperative photoredox catalysis and iron catalysis.