The alcoholysis of racemic enol acetates mediated by lipases in ethanol-hexane gave the corresponding ketones or aldehydes in an optically active form and the stereomodel is proposed for predicting the faster-reacting enantiomer of the enol acetates in this reaction.
|Number of pages||4|
|State||Published - 1 Dec 1996|
- Enantioselective Reaction
- Enol Acetate
- Lipase-Catalyzed Alcoholysis
- Optical Resolution of Aldehyde
- Optical Resolution of Ketone