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filingDate 1993-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63e9a54accafb6667d25a3e8808cc5a3
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publicationDate 1994-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9414764-A1
titleOfInvention Asymmetric process for preparing florfenicol, thiamphenicol, chloramphenicol and oxazoline intermediates
abstract The present invention comprises a process for the asymmetric synthesis of florfenicol, thiamphenicol or chloramphenicol. In an alternative embodiment, the present invention comprises a process for isomerizing of the S,S-isomer of florfenicol to the R,S-isomer (I) by sequentially treating with: (i) a lower alkylsulfonyl chloride and a tertiary amine base; (ii) sulfuric acid and water; (iii) an alkali metal hydroxide. The present invention further comprises a process for regioselectively opening an epoxide to form a threo-oxazoline.
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priorityDate 1992-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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