Title of article :
Preparation of an (−)-ephedrine intermediate through asymmetric reduction of 1-phenyl-1,2-propanedione by anaerobically pre-treated baker’s yeast
Author/Authors :
Lourenço، نويسنده , , Emerson Ricardo Rodrigues Pereira a، نويسنده , , J.Augusto R. and Moran، نويسنده , , Paulo J.S.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Abstract :
The influence of using an anaerobically pre-treated baker’s yeast on the reduction of (R)-1-hydroxy-1-phenyl-2-propanone (2) and (S)-2-hydroxy-1-phenyl-1-propanone (4) was investigated in comparison with non-pre-treated baker’s yeast reduction (control experiments). We observed that there is no significant difference between the anaerobically pre-treated yeast and the control experiment on the reduction rates of 2. On the other hand, the rate of reduction of 4 mediated by the anaerobically pre-treated yeast is much slower than the aerobic experiment. To improve the regioselectivity of reduction of 1-phenyl-1,2-propanedione (1), a baker’s yeast suspension was pre-treated with nitrogen (60 min) followed by oxygen (20 min), to give 2 in 28–31% of yields (96% e.e.) and 3 in 42–62% (>99% e.e.) after 75–90 min of reaction.
Keywords :
Baker’s yeast , (R)-1-hydroxy-1-phenyl-2-propanone , regioselectivity , Ephedrine analogs
Journal title :
Journal of Molecular Catalysis B Enzymatic
Journal title :
Journal of Molecular Catalysis B Enzymatic