Novel Chiral Thiourea Derived from Hydroquinine and l -Phenylglycinol: An Effective Catalyst for Enantio- And Diastereoselective Aza-Henry Reaction

Abstract

A series of chiral thiourea bearing multiple H-bond donors derived from hydroquinine has been reported. The aza-Henry reaction of isatin-derived ketimines and long-chain nitroalkanes catalyzed by these chiral thioureas can achieve high enantioselectivity (78-99% ee) and excellent diastereoselectivity (up to 99:1). This work is the first report on long-chain nitroalkanes as substrates with excellent diastereoselectivity in metal-free catalytic systems.