http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1302207-A
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-85 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-876 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P33-00 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-20 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P33-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P33-00 |
filingDate | 1970-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1973-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1302207-A |
abstract | 1302207 6-Hydroxy-steroids SCHERING AG 27 Jan 1970 [27 Jan 1969] 3929/70 Headings C2C and C2U 6-Hydroxy-3-keto-#<SP>4</SP>-steroids of the pregnane, testololactone and androstane series are prepared by the action of micro-organisms (or enzymes therefrom) of the genus Flavobacterium or of the genus Pseudomonas on the corresponding ring A saturated 3 #-hydroxy-or 3 #-acyloxy- 5,6-epoxy steroids. Novel products are 6α- hydroxy - testololactone and 6α,21 - dihydroxy- 16α - methyl - #<SP>4</SP> - pregnene - 3,20 - dione. Preferred bacterial species are F. dehydrogenano and P. fluorescens. Other substituents and double bonds may also be present in the steroid ring. |
priorityDate | 1969-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 18.