http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100914849-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-822 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2295 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-63 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-66 |
| filingDate | 2007-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2009-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100914849-B1 |
| titleOfInvention | The method for preparation of 2-sulfonyloxy-1-(4-hydroxyphenyl)ethanol derivatives |
| abstract | The present invention provides a 2-sulfonyloxy-1- (4-hydroxy) having high optical activity by asymmetric transfer hydrogenation of α-sulfonyloxy acetophenone derivative in the presence of a rhodium compound catalyst having a pentamethylcyclopentadienyl group and a hydrogen donor. A method for effectively preparing the oxyphenyl) ethanol derivative and a method for producing the ( R ) -optical isomer of a β-adrenoceptor agonist which is a 2-amino-1- (4-hydroxyphenyl) ethanol derivative using the same will be. |
| priorityDate | 2007-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 98.