http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1216190-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B57-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
filingDate 1967-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f85f1ea5bb08e1b631f55dbd3f96e0c4
publicationDate 1970-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1216190-A
titleOfInvention Resolution of enantiomorphic compounds
abstract 1,216,190. Resolution of amino acids. IMPERIAL CHEMICAL INDUSTRIES Ltd. 29 April, 1968 [15 May, 1967], No. 22455/67. Heading C2C. Resolution of an enantiomorphic mixture of a compound in which an amino group is attached to an asymmetric C atom is achieved by interacting the mixture with a single opticallyactive form of a substitution-inert metal coordination compound give a diastereoisomeric interaction product, selectively removing and recovering the enantiomer which is less strongly held by the metal co-ordination compound and recovering the original metal co-ordination compound. The co-ordination compound is preferably [Co<SP>III</SP>EDTA]- and the resolution is advantageously performed in aqueous solution. The less strongly held enantiomer may be selectively removed by precipitation and similarly the bound enantiomer may be released from the interaction product by precipitation. In an example DL-lysine hydrochloride was treated with [l K Co<SP>III</SP> EDTA] and phosphotungstic aid added to precipitate the unbound D-lysine, which was recovered from this precipitate by treatment with barium hydroxide.
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priorityDate 1967-05-15-04:00^^<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: 23.