Publication | Closed Access
Enzymatic Reductions for the Regio- and Stereoselective Synthesis of Hydroxy-keto Esters and Dihydroxy Esters
25
Citations
31
References
2012
Year
Hydroxy-keto EstersEngineeringOrganic Chemistryδ-Hydroxy-β-keto EstersBiosynthesisEnzymatic ReductionsStereoselective SynthesisBiochemistryBiocatalysisDiversity-oriented Synthesisβ-Hydroxy-δ-keto EstersPossible StereoisomersCatalysisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesSynthetic Chemistry
Ketoreductases were utilized for the stereoselective synthesis of δ-hydroxy-β-keto esters, β-hydroxy-δ-keto esters, and β,δ-dihydroxy esters. Seven out of eight possible stereoisomers were obtained from the enzymatic reduction of the corresponding β,δ-diketo ester in high enantio- and diastereomeric excess.
| Year | Citations | |
|---|---|---|
Page 1
Page 1