Ru-NHC-Catalyzed Asymmetric Hydrogenation of 2-Quinolones to Chiral 3,4-Dihydro-2-Quinolones

Direct enantioselective hydrogenation of unsaturated compounds to generate chiral three-dimensional motifs is one of the most straightforward and important approaches in synthetic chemistry. We realized the Ru(II)-NHC-catalyzed asymmetric hydrogenation of 2-quinolones under mild reaction conditions. Alkyl-, aryl- and halogen-substituted optically active dihydro-2-quinolones were obtained in high yields with moderate to excellent enantioselectivities. The reaction provides an efficient and atom-economic pathway to construct simple chiral 3,4-dihydro-2-quinolones. The desired products could be further reduced to tetrahydroquinolines and octahydroquinolones.

Automated summary

The direct enantioselective hydrogenation of 2-quinolones using Ru(II)-NHC catalyst has been achieved, providing alkyl-, aryl- and halogen-substituted optically active dihydro-2-quinolones in high yields with moderate to excellent enantioselectivities. This reaction presents an efficient and atom-economic pathway to construct simple chiral 3,4-dihydro-2-quinolones.