Publication | Open Access
Biocatalytic access to nonracemic γ-oxo esters via stereoselective reduction using ene-reductases
44
Citations
24
References
2016
Year
Chemical EngineeringBiosynthesisEngineeringEnantioselective SynthesisBiochemistryNatural SciencesBiocatalysisEnzyme Catalysisγ-Oxo EstersStereoselective SynthesisBiocatalytic AccessVersatile Chiral IntermediatesStereoselective ReductionAsymmetric Catalysisβ-Unsaturated γ-Keto EstersBiomolecular Engineering
α,β-Unsaturated γ-keto esters were asymmetrically reduced by ene-reductases to yield versatile chiral intermediates in up to 99% ee.
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