Asymmetric synthesis of 2-substituted 4-CHROMANONE (cas 1341-36-2)s using enzyme-catalyzed reactions
-
Add time:09/05/2019 Source:sciencedirect.com
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.
We also recommend Trading Suppliers and Manufacturers of 4-CHROMANONE (cas 1341-36-2). Pls Click Website Link as below: cas 1341-36-2 suppliers
Prev:Intermolecular C–O addition of carboxylic acids to arynes: synthesis of o-hydroxyaryl ketones, xanthones, 4-CHROMANONE (cas 1341-36-2)s, and flavones
Next:Short communicationSynthesis and antibacterial activity of some new 2,3-dimethoxy-3-hydroxy-2-(1-phenyl-3-aryl-4-pyrazolyl)chromanones) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Access to racemic and enantioenriched 3-methyl-4-CHROMANONE (cas 1341-36-2)s: catalysed asymmetric protonation of corresponding enolic species as the key step09/07/2019
- Short communicationSynthesis and antibacterial activity of some new 2,3-dimethoxy-3-hydroxy-2-(1-phenyl-3-aryl-4-pyrazolyl)chromanones09/06/2019
- Intermolecular C–O addition of carboxylic acids to arynes: synthesis of o-hydroxyaryl ketones, xanthones, 4-CHROMANONE (cas 1341-36-2)s, and flavones09/04/2019
- 3-Benzyl-4-CHROMANONE (cas 1341-36-2)s (homoisoflavanones) from bulbs of the ethnomedicinal geophyte Ledebouria revoluta (Hyacinthaceae)09/03/2019
- Topochemical photodimerization of (E)-3-benzylidene-4-CHROMANONE (cas 1341-36-2) derivatives from β-type structures directed by halogen groups09/02/2019
- An efficient synthesis of 4-CHROMANONE (cas 1341-36-2)s09/01/2019
- Bismuth(III) triflate catalyzed tandem esterification–Fries–oxa-Michael route to 4-CHROMANONE (cas 1341-36-2)s08/31/2019
- Enantioselective reduction of 4-CHROMANONE (cas 1341-36-2) and its derivatives by selected filamentous fungi08/30/2019
