http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H07330682-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33dafb5bbc2ec47ebcb7becbbe60f704 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-757 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-753 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-327 |
| filingDate | 1994-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eef749a2113cb0e4271e4963daa4223c |
| publicationDate | 1995-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H07330682-A |
| titleOfInvention | Hexahydroindanecarboxylic acid ester derivative and method for producing the same |
| abstract | (57) [Summary] [Object] To provide a hexahydroindanecarboxylic acid derivative useful as a synthetic intermediate for an optically active steroid compound such as a vitamin D derivative, and a method for producing the same. [Structure] General formula (I) [In the formula, R 1 represents a (1R, 2S, 5R) -8-phenylmenthyl group. ] The hydroindanone derivative represented by the general formula (II) embedded image was sequentially subjected to an isopropenylation reaction, a deoxygenation reaction, an oxidative cleavage reaction of a double bond, and an acetalization reaction. [Wherein, R 1 is as defined above, X and Y each represent a lower alkoxy group, or X and Y together represent a lower alkylenedioxy group. ] The hexahydro indane carboxylic acid derivative shown by these is obtained. |
| priorityDate | 1994-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 210.