Highly Enantioselective Rhodium-Catalyzed Hydrogenation of β-Dehydroamino Acid Derivatives Using Monodentate Phosphoramidites
Journal of the American Chemical Society2002Vol. 124(49), pp. 14552–14553
Citations Over TimeTop 1% of 2002 papers
Abstract
New and very easily accessible monodentate phosphoramidite ligands have been developed that lead to excellent ee's and full conversions in the hydrogenation of (E)- and (Z)-beta-dehydroamino acid derivatives with both aliphatic and aromatic side chains. Particularly, two different catalytic systems were established for (E)-beta-(acylamino)acrylates (98-99% ee) and (Z)-beta-(acylamino)acrylates (92-95% ee) based on phosphoramidites 2 and 3, respectively.
Related Papers
- → Synthesis of new chiral monodentate phosphines and their use in asymmetric hydrogenation(2002)101 cited
- → High Efficiency and Enantioselectivity in the Rh-Catalyzed Conjugate Addition of Arylboronic Acids Using Monodentate Phosphoramidites(2003)113 cited
- → Chiral 1,2,3,4‐Tetrahydro‐1‐naphthylamine‐Derived Phosphine‐Phosphoramidite Ligand (THNAPhos): Application in Highly Enantioselective Hydrogenations of Functionalized CC Bonds(2008)38 cited
- → New chiral diphosphoramidite rhodium(I) complexes for asymmetric hydrogenation(2014)8 cited
- → Cover Feature: Monohydride‐Dichloro Rhodium(III) Complexes with Chiral Diphosphine Ligands as Catalysts for Asymmetric Hydrogenation of Olefinic Substrates (Chem. Eur. J. 40/2020)(2020)1 cited