| Literature DB >> 28872309 |
Fabian Meemken1, Alfons Baiker1.
Abstract
The ease of separation, simple regeneration, and the usually high stability of solid catalysts facilitating continuous production processes have stimulated the development of heterogeneous asymmetric hydrogenation catalysis. The simplest and so far most promising strategy to induce enantioselectivity to solid metal catalysts is their modification by chiral organic compounds, as most prominently represented by the cinchona-modified Pt and Pd catalysts for the asymmetric hydrogenation of activated C═O and C═C bonds. In this Review, we provide a systematic account of the research accomplished in the past decade on noble metal-based heterogeneous asymmetric hydrogenation of prochiral C═O and C═C bonds, including all important facets of these catalytic systems. The advances made are critically analyzed, and future research challenges are identified.Entities:
Year: 2017 PMID: 28872309 DOI: 10.1021/acs.chemrev.7b00272
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622