Abstract
Based on the ever-increasing demand for enantiomerically pure compounds, the development
of efficient, atom-economical, and sustainable methods to produce chiral alcohols
and amines is a major concern. Homogeneous asymmetric catalysis with transition-metal
complexes including asymmetric hydrogenation (AH) and transfer hydrogenation (ATH)
of ketones and imines through dynamic kinetic resolution (DKR) allowing the construction
of up to three stereogenic centers is the main focus of the present short review,
emphasizing the development of new catalytic systems combined to new classes of substrates
and their applications as well.
1 Introduction
2 Asymmetric Hydrogenation via Dynamic Kinetic Resolution
2.1 α-Substituted Ketones
2.2 α-Substituted β-Keto Esters and Amides
2.3 α-Substituted Esters
2.4 Imine Derivatives
3 Asymmetric Transfer Hydrogenation via Dynamic Kinetic Resolution
3.1 α-Substituted Ketones
3.2 α-Substituted β-Keto Esters, Amides, and Sulfonamides
3.3 α,β-Disubstituted Cyclic Ketones
3.4 β-Substituted Ketones
3.5 Imine Derivatives
4. Conclusion
Key words asymmetric hydrogenation - asymmetric transfer hydrogenation - dynamic kinetic resolution
- chiral alcohols - chiral amines - enantioselectivity - diastereoselectivity
