Publication | Closed Access
Axial Chirality Control by 2,4‐Pentanediol for the Alternative Synthesis of C<sub>3</sub>*‐TunePhos Chiral Diphosphine Ligands and Their Applications in Highly Enantioselective Ruthenium‐Catalyzed Hydrogenation of β‐Keto Esters
37
Citations
45
References
2009
Year
Asymmetric Catalysisβ‐Keto EstersEngineeringNatural SciencesDiversity-oriented SynthesisAlternative SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisEfficient StrategyChemistryC 3Synthetic UtilitySynthetic ChemistryStereoselective SynthesisAxial Chirality ControlEnantioselective SynthesisBiomolecular Engineering
Abstract A highly efficient strategy for the synthesis of a series of C 3 *‐TunePhos chiral diphosphine ligands was well established with several remarkable features. The synthetic utility of these ligands was explored for the ruthenium‐catalyzed asymmetric hydrogenation of β‐keto esters. Up to 99% ee values were achieved for the enantioselective synthesis of β‐hydroxy acid derivatives, which are very important chiral building blocks for the synthesis of a variety of natural products and biologically active molecules.
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