A Versatile Route to syn‐ and anti‐α‐Amino β‐Hydroxy Esters from β‐Keto Esters by Dynamic Kinetic Resolution with Ru‐SYNPHOS® Catalyst
- 28 June 2004
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2004 (14), 3017-3026
- https://doi.org/10.1002/ejoc.200400078
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- A Versatile Route to syn‐ and anti‐α‐Amino β‐Hydroxy Esters from β‐Keto Esters by Dynamic Kinetic Resolution with Ru‐SYNPHOS® CatalystEuropean Journal of Organic Chemistry, 2004
- Industrial Methods for the Production of Optically Active IntermediatesAngewandte Chemie-International Edition, 2004
- Stereoselective Synthesis of anti‐β‐Hydroxy‐α‐amino Acids through Dynamic Kinetic ResolutionAngewandte Chemie-International Edition, 2004
- Asymmetric Catalytic Hydrogenation. Design of New Ru Catalysts and Chiral Ligands: From Laboratory to Industrial ApplicationsAccounts of Chemical Research, 2003
- Synthesis and Molecular Modeling Studies of SYNPHOS®, a New, Efficient Diphosphane Ligand For Ruthenium‐Catalyzed Asymmetric HydrogenationEuropean Journal of Organic Chemistry, 2003
- Synthetic applications of the ruthenium-catalyzed hydrogenation via dynamic kinetic resolutionCanadian Journal of Chemistry, 2000
- Total Synthesis of the Biphenomycins; V.1Synthesis of Biphenomycin ASynthesis, 1992
- Amino-acidsPublished by Royal Society of Chemistry (RSC) ,1983
- Synthesis of novel spiro heterocycles. 2-Amino-7-oxa-3-thia-1-azaspiro[5.5]undec-1-enesThe Journal of Organic Chemistry, 1974
- 541. The sphingolipid field. Part I. Synthesis of racemic 2-amino-octadecane-1 : 3-diolsJournal of the Chemical Society, 1951