http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0251324-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_36089addd8e49e968b4c7e13c517dd1c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4075
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-655
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6574
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filingDate 1987-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_074097491faa3d1337cededbf9772453
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_377bbf9115eec5edfc64bfddccb7a24c
publicationDate 1988-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0251324-A2
titleOfInvention Process for the preparation of antibiotics
abstract Intermediate compounds of formulan wherein R and R are the same or different and each represents a lower alkoxy or a -N(R 2 ) 2 group and both R 2 , independently, represent a hydrogen atom or a lower alkyl; the carbon atoms marked by an asterisk are both in R or S configuration; allow to obtain enantioselectively the antibiotic known as Fosfomycin by an epoxidation reaction, carried out in the one or two steps, and a hydrolysis reaction.
priorityDate 1986-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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