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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dfd617dc43a4c986d2dd81e4cb39d9dd
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-14
filingDate 1999-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41355d45758ed1131bb3ebf14596368c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5587ef0fa8513c150f45fea5fb69d90a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5613d2a3e100ba348f0e1ce891f7a9b
publicationDate 2004-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1088825-B1
titleOfInvention Enantiomerically pure substituted oxaaza compounds, salts of the same, and processes for the preparation of both
abstract A process for easily preparing compounds represented by general formula (Ia) which are useful as intermediates for the preparation of antimicrobial compounds, comprising reacting a compound represented by general formula (I) with a ketone and an optically active acid to form a salt of a compound represented by general formula (IIIa) with the optically active acid, converting the salt into a free base and hydrolyzing the free base wherein R1 is hydrogen, alkyl, aryl or aralkyl; and R2 is hydrogen, alkyl, aryl, aralkyl, acyl, alkyloxycarbonyl, aralkyloxycarbonyl or substituted sulfonyl, provided these groups may be further substituted.
priorityDate 1998-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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