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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-234
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-46
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-46
filingDate 1975-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9a2dc1726a7f02b435f72aa9623b7af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a009117c926c6d62bea31d3b0f85d54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c5e3ba84b22ee37e2dbe7d3a437dca7
publicationDate 1985-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1190988-A3
titleOfInvention Method of producing 1/-l-(-)-nu-amino-alpha-oxy-butyryl/kanamycin a
abstract 1- L-(-)-gamma-amino-alpha-hydroxybutynyl -kanamycine A is prepd. by reacting 6'-N-benzyloxycarbonyl kanamycine A with an aldehyde, and condensing the protected intermediate with the N-hydroxy-5-norbornene-2,3-dicarboximide ester of L-gamma-benzyloxycarbonylamino-alpha-hydroxybutyric acid. Prod. is an antibacterial having greater activity than kanamycine A.
priorityDate 1974-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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