http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01224349-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
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filingDate 1988-03-02-04:00^^<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-H01224349-A
titleOfInvention Optically active carboxylic acid derivative and production thereof
abstract NEW MATERIAL:An optically active carboxylic acid derivative expressed by formula I (l is 1 or 2; mark * indicates asymmetric carbon). n EXAMPLE: (+)-4-(1-Hydroxyethyl)benzoic acid. n USE: An intermediate for agricultural chemicals, medicines and veterinary drugs, especially for ferroelectric liquid crystal compounds. n PREPARATION: Optically active esters expressed by formula II (R is H or R"CO; R' and R" are lower alkyl) are hydrolyzed or esters expressed by formula III are asymmetrically hydrolyzed with an esterase having the ability to hydrolyze only either of enantiomers to afford the aimed optically active substance expressed by formula I. Furthermore, the above-mentioned compound can be converted into a liquid crystal compound, excellent as ferroelectric liquid crystal and expressed by formula IV (R 1 and R 2 are alkyl or acyl; Ar is aromatic group, cyclic saturated group, etc.). n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1988-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 24.