Comparison of Chemical and Biochemical Reduction Methods for the Synthesis of (R)-2-Hydroxy-4-Phenylbutyric Acid

Author:

Schmidt E.,Blaser H. U.,Fauquex P. F.,Sedelmeier G.,Spindler F.

Publisher

Springer Netherlands

Reference20 articles.

1. Blaser H.-U., Jalett H.P. and Sedelmeier G. (1986) ‘Enantiomere von Sulfonsaureestern von 4-substituierten 2-Hydroxy-buttersäure-Verbindungen’, EPA 86810255.9

2. Blaser H.U. (1991) ‘Enantioselective Synthesis Using Chiral Heterogeneous Catalysts’. Tetrahedron: Asymmetry 2(9), 843–866

3. Blaser H.U., Jalett H.P. and Wiehl J. (1991) ‘Enantioselective hydrogenation of α-ketoesters with cinchona-modified platinum catalysts: effect of acidic and basic solvents and additives’, J. of Molecular Catalysis 68, 215–222

4. Blaser H.U. and Müller M. (1991) ‘Enantioselective catalysis by chiral solids: Approaches and results’, in Heterogeneous Catalyis and Fine Chemicals II (ed.: Guisnet M. et al), Elsevier Science Publishers B.V., Amsterdam

5. Bradshaw C.W., Wong C.-H., Hummel W. and Kula M.-K. (1991) ‘Enzyme-catalyzed asymmetric synthesis of (S)-2-amino-4-phenylbutanoic acid and (R)-2-hydroxy-4-phenylbutanoic acid’, Bioorg.Chem. 19, 29–39

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