http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1468101-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4ab2d714181eae13dd7cdead6e6fdaf3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-24
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-26
filingDate 2003-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd09628e7e7027f44c2f9b762b7232df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66038e2946584411ae4b167315a22999
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c15db21421396704aeacccd4cb32439
publicationDate 2006-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1468101-B1
titleOfInvention Process for preparing chiral aromatic alpha-hydroxy ketones using 2-hydroxy-3-oxoacid synthase
abstract A biotransformation process for preparing chiral aromatic-hydroxy ketones in high yields is described, using 2-hydroxy-3-oxoacid synthase, such as AHAS or TSAS. Optionally substituted arylaldehydes and -oxoacids react in this process to provide pure enantiomers, useful as synthons in the production of various drugs, an example being (R)-phenylacetyl carbinol.
priorityDate 2002-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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