http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01224350-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76 |
filingDate | 1988-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a48cb8be90afcd3b9f41ff9c47b2ea2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf1279d98782c00b7ed8767a8017b2f8 |
publicationDate | 1989-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H01224350-A |
titleOfInvention | Optically active 1-phenylethanol derivative and production thereof |
abstract | NEW MATERIAL:An optically active 1-phenylethanol derivative expressed by formula I (R is H or acetyl; R' is H, lower alkyl, lower alkoxyl or halogen; mark * indicates asymmetric carbon). n EXAMPLE: Benzyl (-)-4-(1-acetoxyethyl)phenylcarboxylate. n USE: An intermediate for medicines, agricultural chemicals, etc., particularly organic electronic material, especially an intermediate for liquid crystal compounds. n PREPARATION: Ketones expressed by formula II are reduced with a reducing agent to provide alcohols expressed by formula III, which are subsequently reacted with acetic acids to afford dl-esters expressed by formula IV. The resultant dl-esters are then asymmetrically hydrolyzed with an esterase having the ability to hydrolyze either of enantiomers thereof to provide the aimed optically active substance expressed by formula I. n COPYRIGHT: (C)1989,JPO&Japio |
priorityDate | 1988-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.