http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2004035539-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-08 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D477-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06 |
| filingDate | 2003-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2006-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-WO2004035539-A1 |
| titleOfInvention | Process for producing carbapenems and intermediates used for the production |
| abstract | The present invention is useful as a prodrug-type oral carbapenem agent represented by the following formula (XI) [wherein R 2 represents a group that can be easily removed by decomposition in vivo, and R 4 represents 1 -Represents (1,3-thiazolin-2-yl) azetidin-3-yl or pyrrolidin-2-one-4-yl], and a synthetic intermediate used in the production. According to the method of the present invention, the compound can be produced at a lower cost, and industrial production can be advantageously performed. |
| priorityDate | 2002-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 166.