Silica gel-immobilised chiral 1,2-benzenedisulfonimide: a Bronsted acid heterogeneous catalyst for enantioselective multicomponent Passerini reaction

A chiral heterogeneous catalyst derivative of (-)-4,5-dimethyl-3,6-bis(1-naphthyl)-1,2-benzenedisulfonimide is proven here to be efficient in a three-component asymmetric Passerini protocol, carried out in a deep eutectic solvent. Reaction conditions are mild and green, while enantioselectivity is excellent. The catalyst was easily recovered and reused with no decrease in its catalytic activity.

Automated summary

A chiral heterogeneous catalyst proved to be efficient in a three-component asymmetric Passerini protocol conducted in a deep eutectic solvent. The reaction conditions were mild and environmentally-friendly, with excellent enantioselectivity. The catalyst was easily recovered and reused without any loss in catalytic activity.