http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9622959-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C57-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-487
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-64
filingDate 1996-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b49d09941e928408f754fd576d245487
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d23909c4284c735b9093c55e63a0ac9
publicationDate 1996-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9622959-A1
titleOfInvention Preparation of optically active aliphatic carboxylic acids
abstract A process for the separation of a racemic mixture of certain aliphatic carboxylic acids or esters thereof is disclosed. The process comprises: (i) forming a diastereomeric salt by reaction comprising said racemic mixture of a C1 to C6 linear or branched aliphatic carboxylic acid and an amount of an N-alkyl-D-glucamine that is sufficient to react with one of the enantiomers of the racemic mixture; (ii) precipitating from the reaction solution formed in step (i) the diastereomeric salt; (iii) separating said precipitated diastereomeric salt; (iv) decomposing the salt into its enantiomeric component and its organic base component; and (v) isolating a substantially pure enantiomer from said decomposed salt.
priorityDate 1995-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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