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Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase
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Citations
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References
2011
Year
Bioorganic ChemistryEngineeringContiguous Stereogenic CentersOrganic ChemistryChemistryStyrene MonooxygenaseEnantio-selective EpoxidationBiosynthesisGlycidol DerivativesStereoselective SynthesisBiochemistryBiocatalysisSecondary Allylic AlcoholsCatalysisNatural Product SynthesisAsymmetric CatalysisStyrene Monooxygenase Styab2Enantioselective SynthesisBiomolecular EngineeringNatural Sciences
Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
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