Horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol
1998
Abstract
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)]
Details
Title
Horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol
Author(s)
Laib, Taoues ; Ouazzani, Jamal ; Zhu, Jieping
Published in
Tetrahedron: Asymmetry
Volume
9
Issue
1
Pages
169-178
Date
1998
ISSN
0957-4166
Keywords
Hydrolysis (biol.; horse liver esterase catalyzed enantioselective hydrolysis of N; O-diacetyl-2-amino-1-arylethanol); Resolution (enzymic; horse liver esterase catalyzed enantioselective hydrolysis of N; O-diacetyl-2-amino-1-arylethanol); Solvent effect (horse liver esterase catalyzed enantioselective hydrolysis of N; O-diacetyl-2-amino-1-arylethanol); acetylaminoarylethanol hydrolysis horse liver esterase
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
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)
25-7
Benzene, Its Derivatives, and Condensed Benzenoid Compounds
Institut de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr.
Journal
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
LSPN
Record Appears in
Scientific production and competences > SB - School of Basic Sciences > ISIC - Institute of Chemical Sciences and Engineering > LSPN - Laboratory of synthesis and natural products
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Published
Peer-reviewed publications
Work outside EPFL
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Record creation date
2010-11-25