Resolution of (R,S)-4-Hydroxy-3-methyl-2-(2-propenyl)-2-cyclopenten-1-one Catalyzed by Lipase in Ionic Liquid
-
Add time:07/16/2019 Source:sciencedirect.com
The resolution of (R,S)-4-hydroxy-3-methyl-2-(2-propenyl)-2-cyclopenten-1-one ((R,S)-HMPC) was studied using ionic liquids or vinyl acetate as the reaction medium. The effects of the reaction medium, water activity, temperature, pH value, and the cosolvent on the resolution were studied. The results showed that the ionic liquid [bmim]PF6 was suitable for the reaction, and the initial rate of lipase in [bmim]PF6 was 18.48 μmol/(g·min), which was considerably higher than that in vinyl acetate (9.18 μmol/(g·min)). The half-life of lipase in the ionic liquid was 74.53 h, which was higher than that in vinyl acetate (64.29 h), but the conversion of (R,S)-HMPC in ionic liquids was lower than that in vinyl acetate. The addition of an acryl donor could improve the conversion of (R,S)-HMPC in ionic liquids. The optimum reaction conditions in [bmim]PF6 were: water activity 0.17, 40°C, and pH = 7, the same as those in vinyl acetate. When the cosolvent was added to the reaction system, the conversion in [bmim]PF6 decreased, whereas that in vinyl acetate increased, which might be attributed to the different properties of the reaction media.
We also recommend Trading Suppliers and Manufacturers of N-Methyl-N'-(2-propenyl)-1,2-hydrazinedicarbothioamide (cas 5638-74-4). Pls Click Website Link as below: cas 5638-74-4 suppliers
Prev:Synthesis, structural and conformational studies of Z- and E-isomers of fluorinated C-6 isobutenyl N-methyl thymine derivatives
Next:The synthesis and enzymic hydrolysis of (E)-2-[2,3-2H2]propenyl glucosinolate: Confirmation of the rearrangement of the thiohydroximate moiety) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis and antibacterial activities of 6-O-methylerythromycin A 9-O-(3-aryl-2-propenyl) oxime ketolide, 2,3-enol ether, and alkylide analogues07/19/2019
- Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II: 3-O-(3-Aryl-2-propenyl)leucomycin analogues07/18/2019
- The synthesis and enzymic hydrolysis of (E)-2-[2,3-2H2]propenyl glucosinolate: Confirmation of the rearrangement of the thiohydroximate moiety07/17/2019
- Synthesis, structural and conformational studies of Z- and E-isomers of fluorinated C-6 isobutenyl N-methyl thymine derivatives07/15/2019
- The α-asarone/clofibrate hybrid compound, 2-methoxy-4-(2-propenyl)phenoxyacetic acid (MPPA), is endowed with neuroprotective and anticonvulsant potentialities07/14/2019
- Synthesis of cis-2-alkoxycyclopropylamines via intramolecular cyclization of 2-azaallylic anions derived from alkoxybrominated N-(arylidene)-2-methyl-2-propenylamines07/13/2019
- Theoretical DFT, vibrational and structural characterization of 1-propenyl-2-methylbenzimidazole and its isomers07/12/2019
- PEPPSI-type 2-methyl-2-propenyl-functionalized N-heterocyclic carbene-palladium complexes: Synthesis, structural characterization and catalytic activity on Suzuki–Miyaura reaction07/11/2019


