Abstract
Incubations of the fungus Mortierella isabellina NRRL 1757 with 3-oxo-3-phenylpropanamide, 3-oxobutanamide and with some of their N-alkyl derivatives afford the corresponding (S)-3-hydroxyamides usually in high chemical yields and enantiomeric excesses.
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CITATION STYLE
APA
Quirós, M., Rebolledo, F., Liz, R., & Gotor, V. (1997). Enantioselective reduction of β-keto amides by the fungus Mortierella isabellina. Tetrahedron Asymmetry, 8(18), 3035–3038. https://doi.org/10.1016/S0957-4166(97)00378-9
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