http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-506554-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c902faf6ae746c51fc8010672fc22894 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-16 |
| filingDate | 1968-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0ac442e5dac7d8e79ca6ae9e2f90d85 |
| publicationDate | 1971-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-506554-A |
| titleOfInvention | Process for the preparation of lincomycin 7-esters |
| abstract | Process: R- - = an aliphatic carboxylic acid residue (C2-C18) Lincomycin-7-acylates and -carboxylates have essentially the same antibacterial spectrum as the antibiotic lincomycin and may be used as antibacterial agents. Lincomycin-7-acetate inhibits the growth of Staph. aureus and may be used as disinfecting agent for infected dinner-things. The 7-acylates and 7-carboxylates may also be used for inhibiting the growth of Gram-pos. spores on agar plates in the separation of fungi, yeasts Streptomycetes and Gram-neg. organisms. The new intermediates 2, 3, 4-tris-O(trimethylsilyl) lincomycin 7-acylates and -carboxylates (IV) are used in the preparation of (V). The new process gives much higher yields than known processes. |
| priorityDate | 1967-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 282.