http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0499376-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-34
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-00
filingDate 1992-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_505035668feb188fa82d416ffaf032ae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f5bf50d82a3d66363312de4ed2e19cb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b96caeb8e0f35af509505513e9da0ee6
publicationDate 1992-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0499376-A1
titleOfInvention Precipitation-induced asymmetric transformation of chiral alpha-amino acids and salts thereof
abstract The present invention provides a method for resolving a mixture of optically active isomers of an α-amino acid to obtain the preferred optically active isomer. The mixture of isomers is contacted with at least one chiral resolving agent in an organic acid, which is at least a partial solvent for the α-amino acid, and in the presence of a mineral acid, which is present in a quantity which does not protonate the NH₂ functionality of the α-amino acid to an extent that diastereomer interconversion is substantially prevented, and in the presence of a catalytic amount of an aromatic aldehyde. The contacting results in simultaneous resolution of a desired diastereomer and interconversion of the remaining undesired diastereomer, to provide a very high yield of the desired diastereomer having a very high optical purity.
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priorityDate 1991-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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