http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8302002-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-587 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 |
filingDate | 1981-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1982-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-8302002-A1 |
titleOfInvention | A PROCEDURE FOR THE PREPARATION OF NEW CEPHALOSPORIN DERIVATIVES. |
abstract | PROCEDURE FOR OBTAINING DERIVATIVES OF CEPHALOSPORIN AND ITS PHYSIOLOGICALLY COMPATIBLE ACID ADDITION SALTS, OF FORMULA (I), IN WHICH R IS METHYL OR ETHYL; R IS HYDROGEN OR METHYL; AND R IS ALKYL C <003> OR ALCOXY C <003>. CONSISTS OF THE REACTION OF A COMPOUND OF FORMULA (II) OR A REACTIVE DERIVATIVE OF THE SAME WITH A COMPOUND OF FORMULA R <024> COOCHR B, IN WHICH A IS OXYGEN O = NOR; R IS AMINO OR PROTECTED AMINO; R IS HYDROXI AND B IS THE GROUP OF FORMULA (III) OR R IS THE GROUP OF FORMULA (IV) AND B IS HALOGEN; AND THE OTHER SYMBOLS HAVE THE SAME MEANING AS IN THE FORMULA (I). THE REACTION IS CARRIED OUT IN AN INERT SOLVENT AT ROOM TEMPERATURE. THESE COMPOUNDS HAVE PHARMACOLOGICAL APPLICATIONS FOR THEIR ANTIBACTERIAL ACTIVITY. |
priorityDate | 1980-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 17.