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Volumn 57, Issue 23, 2001, Pages 4841-4848
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Synthesis of enantiomers of indanoxazolidinone based on the lipase-catalyzed resolution of the corresponding N-carbamylamino derivative
a
KEIO UNIVERSITY
(Japan)
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Author keywords
Enzymes and enzyme reactions; Hydrolysis; Nitroso compounds; Oxazolidinones
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Indexed keywords
1 (N' ACETYL N CARBAMYLAMINO) 2 INDANOL;
1 (N' ACETYL N CARBAMYLAMINO) 2 INDANOL O ACETATE;
1 (N' ACETYL N CARBAMYLAMINO) 2 INDANOL O CHLOROACETATE;
1 (N' CHLOROACETYL N CARBAMYLAMINO) 2 INDANOL;
1 (N' CHLOROACETYL N CARBAMYLAMINO) 2 INDANOL O CHLOROACETATE;
1 AMINO 2 INDANOL;
1 N CARBAMYLAMINO 2 INDANOL;
ACETIC ACID DERIVATIVE;
ACETONE;
AMINE;
AMINOALCOHOL;
BETA CYCLODEXTRIN;
BUFFER;
CHIRAZYME;
INDANO[1,2 D]OXAZOLIDINONE DERIVATIVE;
INDINAVIR;
N CARBAMYLAMINO DERIVATIVE;
OXAZOLIDINONE DERIVATIVE;
TRIACYLGLYCEROL LIPASE;
UNCLASSIFIED DRUG;
ACETYLATION;
ARTICLE;
BURKHOLDERIA CEPACIA;
CATALYSIS;
CHEMICAL REACTION;
CYCLIZATION;
ENANTIOMER;
ENZYME ACTIVITY;
HYDROLYSIS;
NITROSATION;
PRECURSOR;
PRIORITY JOURNAL;
RACEMIC MIXTURE;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STOICHIOMETRY;
TEMPERATURE;
TIME;
BURKHOLDERIA CEPACIA;
PSEUDOMONAS;
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EID: 0035806158
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00454-9 Document Type: Article |
Times cited : (14)
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References (43)
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