| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_52a65b677bbedbe7bf090dd556a7cc43 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-004
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-62 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 |
| filingDate |
1998-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55fd1a1b74137009d248fc0e9988bf9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51e831f3661ff88cdf33b5ced99ac9cb |
| publicationDate |
1999-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-0908522-A1 |
| titleOfInvention |
A method for producing an optically active 2-alkanol |
| abstract |
Both enantiomers of optically active 2-alkanol are produced byntransesterification reaction of racemic 2-alkanol and aliphatic acid 2,2,2-trichloroethyleslernin the presence of enzyme derived from Candida antarctica. n Both enantiomers of optically active 2-alkanol, which are useful asnstarting materials of liquid crystal materials and have optical purity of 99% ornmore, can be efficiently produced. |
| priorityDate |
1997-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |