The reduction of 2-chloro-1-phenyl-2-propen-1-one (2) by baker's yeast (Sac
charomyces cerevisiae) was performed under various reaction conditions, suc
h as the addition of allyl alcohol, sucrose, thermal pre-treatment of the c
ells and use of a citrate buffer at pH 4.0. 2-Chloro-1-phenyl-1-propan-1-on
e (3) was produced after 2 h in a poor enantiomeric excess (ee) while after
a longer period of fermentation, the compounds IR,2R- and IR,2S-2-chloro-1
-phenylpropan-1-ol (4) were obtained at 80-90 and 28-63% ee. (C) 2001 Elsev
ier Science B.V. All rights reserved.