http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SE-7713521-L

Outgoing Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-546
filingDate 1977-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ef31b2717b4ef051fa6f6edb5c488f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4595f1f8ffb696ed5946c77bb3b81e6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_243679ba88b47b4ae81ce490833005b2
publicationDate 1978-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SE-7713521-L
titleOfInvention PROCEDURE FOR MANUFACTURE OF ANTIBIOTICS
abstract Antibiotic compounds of the general formula <IMAGE> (I) [wherein R is a phenyl, thienyl or furyl group; Ra and Rb, which may be the same or different, are each selected from hydrogen, C1-4 alkyl, C2-4 alkenyl C3-7 cycloalkyl, phenyl, naphthyl, thienyl, furyl, carboxy, C2-5 alkoxycarbonyl and cyano, or Ra and Rb together with the carbon atom to which they are attached from a C3-7 cycloalkylidene or cycloalkenylidene group; Rc is hydrogen or lower alkyl; Rd is hydroxy, lower alkoxy, aralkoxy or aryloxy; m and n are each 0 or 1 such that the sum of m and n is 0 or 1; and P is selected from a hydrogen atom, a halogen atom and various organic groups] and non-toxic derivatives thereof.
priorityDate 1976-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 28.