The effect of catechin derivatives on the enantioselectivity of lipase-catalyzed hydrolyses of alkynol benzoate esters
-
Add time:07/16/2019 Source:sciencedirect.com
Polyphenols, such as (+)-catechin and pyrogallol could be used to enhance stereochemical control in the lipase-catalyzed hydrolysis of alkynol benzoate esters, leading to increased enantioselectivities in the kinetic resolution of alkynols with lipase Amano AH.
We also recommend Trading Suppliers and Manufacturers of PROPARGYL BENZOATE 98 (cas 6750-04-5). Pls Click Website Link as below: cas 6750-04-5 suppliers
Prev:Intramolecular iminium ene reaction with Cu(I) catalysts: facile formation of 4-amino-3-methylenechromans from O-propargyl salicylaldehydes and dialkylamines
Next:An efficient and simple approach for the synthesis of pyranopyrazoles using imidazole (catalytic) in aqueous medium, and the vibrational spectroscopic studies on 6-amino-4-(4′-methoxyphenyl)-5-cyano-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazole using density functional theory) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Intramolecular iminium ene reaction with Cu(I) catalysts: facile formation of 4-amino-3-methylenechromans from O-propargyl salicylaldehydes and dialkylamines07/15/2019
- First total synthesis of modiolide A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone07/14/2019
- Silylation–desilylation of propargyl amides: rapid synthesis of functionalised aldehydes and β-lactams07/13/2019
- MAO enzymes inhibitory activity of new benzimidazole derivatives including hydrazone and propargyl side chains07/12/2019
- Gold(I)-catalyzed enantioselective [3+2] and [3+3] cycloaddition reactions of propargyl acetals/ketals07/11/2019
-
Health and Chemical more >


