http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012506862-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7052 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08 |
| filingDate | 2009-10-23^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2012-03-22^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2012506862-A |
| titleOfInvention | Method for synthesizing macrolide compounds |
| abstract | The present invention relates to a method for synthesizing macrolide compounds that are known to have antibacterial activity and are useful for the treatment of bacterial infections in mammals. More specifically, the present invention relates to a method for synthesizing a macrolide antibiotic, gamithromycin, using a novel catalyst configuration, chemical structure and / or method. One embodiment of the invention can include advancing multiple chemical reactions without isolating chemical intermediates. Thus, multiple reactions can be performed in a single reactor, allowing a significant reduction in cycle time. The present invention also provides a novel method for inhibiting degradation during isolation of the structure of a pharmaceutical composition. [Selection figure] None |
| priorityDate | 2008-10-24^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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