Abstract
Both the enantiomers of frontalin were synthesized from a tert-alcoholchiral building block, (/?)-2-acetoxymethylglycidol, prepared by an enzyme-catalyzed reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 61-64 |
| Number of pages | 4 |
| Journal | Natural Product Letters |
| Volume | 4 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Feb 1994 |
Keywords
- (R)-2-Acetoxymethylglycidol
- Asymmetric hydrolysis
- Enantiomers
- Enantioselective synthesis
- Frontalin
- Lipase
- tert-Alcoholchiral building block