Publication | Closed Access
Enantioselective Synthesis of <i>syn</i>- and <i>anti</i>-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation
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Citations
22
References
2010
Year
Anti DiastereomersStereogenic CentersBioorganic ChemistryEngineeringBiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryHigh YieldStereoselective SynthesisChemistryNatural Product SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
β-Aminoketones obtained from imines in an organocatalytic Mannich reaction were transformed to enantio- and diastereomerically pure 1,3-aminoalcohols with two stereogenic centers via a combined reduction/dynamic kinetic asymmetric transformation. Both syn and anti diastereomers were obtained in high yield, dr, and ee.
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