http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01275594-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_46e48a70f5682ddc8379f7145b9693a9 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-234 |
| filingDate | 1988-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8032beb3c72be86cf501ee87bcc53d24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_450274491285cabbaeca12d9e16aec42 |
| publicationDate | 1989-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H01275594-A |
| titleOfInvention | Production of kanamycin derivative |
| abstract | PURPOSE: To obtain the subject compound having antimicrobial activity, by reacting a kanamycin A derivative with L-(-)-α-hydroxy-γ-phthalimidobutyric acid, etc., and eliminating an amino-protecting and phthaloyl groups of the resultant product. n CONSTITUTION: A kanamycin A derivative expressed by formula I (R is amino- protecting group) is reacted with L-(-)-α-hydroxy-γ-phthalimidobutyric acid expressed by formula II or a reactive derivative thereof to provide a compound expressed by formula III. The amino-protecting and phthaloyl groups are then eliminated and, as desired, further converted into an addition salt with an acid to afford the aimed compound expressed by formula IV. n COPYRIGHT: (C)1989,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014051515-A |
| priorityDate | 1988-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 21.