http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3920696-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04 |
| filingDate | 1973-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1975-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f67ce42eed1185bb4a50e9ffa21c63fc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b651157b1b567b81e6fd950d1d6a4336 |
| publicationDate | 1975-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-3920696-A |
| titleOfInvention | 2s-carboxyalkylthio-3r-imidoazetidin-4-ones and compounds useful in their preparation |
| abstract | 2S-Carboxyalkylthio-3R-imidoazetidin-4-ones can be prepared by the sequential conversion of 2-halo-1(1''-(protected)carboxy-2''methylprop-1''-enyl)-3R-imidoazetidin-4-ones to 2-halo-1(protected)carboxyoxalyl-3R-imidoazetidin-4-ones, which are converted to 2-halo-3R-imidoazetidin-4-ones, which are converted to 2S-(protected)carboxyalkylthio-3R-imidoazetidin-4-ones, which are converted to the title compounds. The title compounds exhibit antibacterial activity. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4144333-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4200571-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4115383-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0254578-A1 |
| priorityDate | 1973-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 104.