Stereoselective hydrogenation of tetrasubstituted olefins is an attractive method to access
compounds with two contiguous stereocenters. However, homogeneous catalysts for …

As established by Baiker and co-workers, pantoyl-naphthylethylamine (PNEA) is an efficient
synthetic chiral modifier for the asymmetric hydrogenation of ketopantolactone (KPL) to …

Stereoselectivity in heterogeneous hydrogenation of olefins and arenes is typically dictated
by the steric properties of the organic substrate, and the inherent steric preference is difficult …

The exigent need to develop new asymmetric hydrogenation catalysts is universally
acknowledged, and many new feasible strategies for the design and synthesis of such …

Surface modification of metal nanoparticles (NPs) with organic molecules has attracted
considerable attention as an effective methodology for designing highly selective …

The enantioselective hydrogenation of arenols to corresponding chiral cyclic alcohols
remains a challenge because of their aromaticity and the difficulty in controlling the regio …

The ruthenium-catalyzed homogeneous hydrogenation of carbonyl groups has established
itself as a mature synthetic method on an academic and industrial scale [1] for the selective …

Enantiopurity is of crucial importance for the production of fine chemicals, pharmaceuticals,
agrochemicals, flavors, and fragrances.[1] The great demand for, and the limited natural …

Asymmetric hydrogenation has evolved as one of the most powerful tools to construct
stereocenters. However, the asymmetric hydrogenation of unfunctionalized tetrasubstituted …

Asymmetric hydrogenation of heteroaromatic compounds has captured considerable
attention because it offers straightforward and environmentally benign routes to optically …