http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-949669-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S8-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-929
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-006
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-40
filingDate 1962-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1964-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-949669-A
titleOfInvention Process for the production of optically-active ยช -alkyl-substituted phenoxyacetic acids and the alkylamides thereof
abstract The invention comprises the alkylamides of optically active a -alkyl substituted phenoxyacetic acids, specifically L(-) -a - phenoxybutyryl isobutylamide and a process for the production of the optical isomers of said acids by converting the racemic acid to its racemic alkylamide, subjecting the latter in an aqueous medium to the action of a fungus of the genus Fusarium to effect complete hydrolysis of one of the isomeric alkylamides in the racemate and separating and recovering the enantiometic a -alkyl substituted phenoxyacetic acid thus produced. The hitherto unhydrolysed amide may then be hydrolysed for recovery of the enantiomeric acid, e.g. L-a -phenoxybutyric acid; the latter may be converted to its acid chloride with SOCl2.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5034329-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5089405-A
priorityDate 1961-09-16-04:00^^<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.