Abstract
2-Substituted 4-chromanones were synthesized in their optically active forms. The chiral intermediates were obtained via lipase-catalyzed enantioselective reactions. Lipase and esterase were also used for the hydrolysis of ester moieties of the precursors of the target compounds under mild conditions.
Original language | English |
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Pages (from-to) | 93-102 |
Number of pages | 10 |
Journal | Journal of Molecular Catalysis B: Enzymatic |
Volume | 54 |
Issue number | 3-4 |
DOIs | |
State | Published - 2008/08 |
Keywords
- Asymmetric synthesis
- Chromanones
- Enzyme
- Hydrolysis
- Resolution
ASJC Scopus subject areas
- Catalysis
- Bioengineering
- Biochemistry
- Process Chemistry and Technology