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Volumn 57, Issue 4, 2001, Pages 695-701
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Microbiological transformations. Part 45: A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: Elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process
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Author keywords
Aspergillus niger; Biotransformation; Chiral synthons; Eliprodil; Enantioselective hydrolysis; Epoxide hydrolase; Hydrolytic kinetic resolution; Solanum tuberosum
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Indexed keywords
4 CHLOROSTYRENE OXIDE;
ELIPRODIL;
EPOXIDE HYDROLASE;
STYRENE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
ASPERGILLUS NIGER;
CATALYSIS;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
HYDROLYSIS;
NONHUMAN;
PRIORITY JOURNAL;
RACEMIC MIXTURE;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STOICHIOMETRY;
ASPERGILLUS NIGER;
SOLANUM TUBEROSUM;
TUBEROSUM;
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EID: 0035924935
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(00)01032-2 Document Type: Article |
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Times cited : (90)
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References (30)
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