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 |
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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