PREPARATION OF BOTH THE ENANTIOMERS OF 3-OCTANOL, THE PHEROMONE OF VARIOUS SPECIES OF ANTS, BY ENANTIOSELECTIVE HYDROLYSIS WITH PSEUDOMONAS-CEPACIA LIPASE
M. Kamezawa et al., PREPARATION OF BOTH THE ENANTIOMERS OF 3-OCTANOL, THE PHEROMONE OF VARIOUS SPECIES OF ANTS, BY ENANTIOSELECTIVE HYDROLYSIS WITH PSEUDOMONAS-CEPACIA LIPASE, Bioscience, biotechnology, and biochemistry, 58(3), 1994, pp. 598-599
The two enantiomers of 3-octanol (3), the pheromone of a number of spe
cies of ants, were synthesized with a high enantiomeric purity of almo
st 100% e.e. via an enzymatic two-step hydrolysis catalyzed by Pseudom
onas cepacia lipase in an acetone-water solvent system.