Horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol

N,O-Diacetyl-2-amino-1-arylethanol can be efficiently resolved by horse liver esterase (HLE). A remarkable org. co-solvent effect on the enantioselectivity of HLE was obsd. [on SciFinder (R)]


Published in:
Tetrahedron: Asymmetry, 9, 1, 169-178
Year:
1998
Keywords:
Note:
CAN 128:217145
25-7
Benzene, Its Derivatives, and Condensed Benzenoid Compounds
Institut de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr.
Journal
0957-4166
written in English.
202120-58-9P; 202120-59-0P Role: BPN (Biosynthetic preparation), PUR (Purification or recovery), RCT (Reactant), BIOL (Biological study), PREP (Preparation), RACT (Reactant or reagent) (horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol); 9016-18-6 (Carboxyl esterase) Role: CAT (Catalyst use), USES (Uses) (horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol); 7568-93-6; 36394-75-9 ((S)-2-Acetoxypropionyl chloride); 42564-51-2 (4-Fluoro-3-nitrobenzaldehyde) Role: RCT (Reactant), RACT (Reactant or reagent) (horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol); 3306-05-6P; 55044-72-9P; 202120-55-6P; 202120-56-7P; 202120-57-8P; 204264-61-9P; 204264-63-1P; 204264-64-2P; 204264-65-3P; 204264-66-4P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol); 155073-71-5P; 157379-64-1P; 204264-57-3P; 204264-58-4P; 204264-59-5P; 204264-60-8P; 204264-62-0P Role: SPN (Synthetic preparation), PREP (Preparation) (horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol); 64-17-5 (Ethanol); 67-64-1 (Acetone); 108-20-3 (Isopropyl ether); 110-54-3 (Hexane) Role: NUU (Other use, unclassified), USES (Uses) (solvent; horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol)
Laboratories:




 Record created 2010-11-25, last modified 2018-03-17


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