http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0041656-A3
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-517 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-517 |
| filingDate | 1981-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1982-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0041656-A3 |
| titleOfInvention | Cyclohexanone derivatives and preparation thereof |
| abstract | Novel cyclohexanone derivatives of general formula: n n(wherein R¹ is a hydrocarbon group of 1 to 15 carbon atoms) nand new cyclohexanone derivatives of general formula : n n(wherein R¹ and R² each is a hydrogen group of 1 to 15 ncarbon atoms) are produced by an electrooxidative coupling nof 1,3-cyclohexanedione with a vinyl ether of general formula: nCH₂=CH-O-R¹ n(wherein R¹ is as defined above) in the presence or absence of nan alcohol of general formula: nR²OH n(wherein R² is as defined above). These new cyclohexanone nderivatives can be easily converted to N-substituted or nunsubstituted-4-oxo-4,5,6,7-tetrahydroindoles, which are of nvalue as intermediates for the production of N-substituted or nunsubstituted-4-hydroxyindoles and, thence, to pindolol and nits analogs. |
| priorityDate | 1980-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.