Highly stereoselective reduction of 4-Aryl-2-oxo but-3-enoic carboxylic esters by plant cell culture of Daucus carota☆
-
Add time:09/01/2019 Source:sciencedirect.com
A highly enantioselective preparation (92–99% enantiomeric excess, 100% conversion) of various 4-aryl-2-hydroxy but-3-enoic carboxylic acid esters from the corresponding 4-phenyl-2-keto but-3-enoic acid esters mediated by plant cell cultures of Daucus carota under mild and environmentally benign conditions in aqueous medium is described.
We also recommend Trading Suppliers and Manufacturers of 3-Butenoic acid, 3-chloro-2-hydroxy-, ethyl ester (cas 18418-17-2). Pls Click Website Link as below: cas 18418-17-2 suppliers
Prev:Optimization of asymmetric hydrogenation of 3-phenyl-3-butenoic acid catalyzed by rhodium(I)-4,5-bis[(diphenylphosphino)methyl]-2,2-dimethyldioxolane (DIOP)☆☆☆
Next:Urea functionalized surface-bonded sol-gel coating for on-line hyphenation of capillary microextraction with high-performance liquid chromatography) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Optimization of asymmetric hydrogenation of 3-phenyl-3-butenoic acid catalyzed by rhodium(I)-4,5-bis[(diphenylphosphino)methyl]-2,2-dimethyldioxolane (DIOP)☆☆☆08/31/2019
- Induction of DNA strand breaks by 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone and humic substances in relation to glutathione and calcium status in human white blood cells08/30/2019
-
Health and Chemical more >


