http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0282221-A2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-487
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-487
filingDate 1988-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2d13a66d79cf9a6a5f4b50f6d063c1e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_918dcdf1dd46ce3883fad9a32b7f2fa5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_719b9499e69b3427d8cc79d865715645
publicationDate 1988-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0282221-A2
titleOfInvention Method for racemization of optically active chrysanthemic acid or its ester
abstract Racemization of an optically active chrysanthemic acid or its ester of the formula: <CHEM> wherein R represents a hydrogen atom, an alkyl group of 1-20 carbon atoms, a cycloalkyl group of 3-20 carbon atoms or an aralkyl group of 7-20 carbon atoms and * mark indicates asymmetric carbon atom, is effected by contacting the acid or its ester with at least one compound selected from the group consisting of a carboxylic acid bromide, a silicon bromide, an S-bromine compound, and N-bromine compound, a halo-bromine compound and an SH compound in the presence of a peroxide or an azo compound.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6750370-B2
priorityDate 1987-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 510.