Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_da54f7ebbd2d9d8a82f92aca4d1b4e48 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-921 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-911 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-939 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P17-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-002 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C405-0083 |
classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-845 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-645 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C405-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 |
filingDate |
1987-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
1992-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a21fa494840c63368f2d51986105f62a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e8d80282b67bad4a4a68d337f3d45b5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d6146143ac7dbed77bcf2b0cd42d38b |
publicationDate |
1992-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
DE-3780277-D1 |
titleOfInvention |
STEREO-SPECIFIC KETOR REDUCTION OF BICYCLOOCTANDION-CARBONIC ACID ESTERS BY MICRO-ORGANISMS. |
abstract |
Prodn. of 3alpha-hydroxy-bicyclooctane cpds. of formula (I) comrpises treating the racemic oxo cpd. (II) with a Rhizopus, Thodotorula or Candida strain. Where the strain used reduces the (-) form, the unchanged (+)-(II) is reduced subsequently by a chemical or microbiological process. A = CH2 or CH-COOR; B = O or -O-X-O-; X = opt. branched 1-7C alkylene; R = 1-6C alkyl or benzyl. |
priorityDate |
1986-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |