http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2481839-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d9cb217f83556ce2a418344c2d485415
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P13-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-005
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
filingDate 2003-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d4605721244949fbbaa726b126ff952
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaec4e9530bcaa97b1c7788d3a408a66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15c27e6c57bd47bfc886523325e00b19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6d1bb125295059ffa0cc885b75ad712
publicationDate 2003-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2481839-A1
titleOfInvention Process for producing either optically active n-substituted .beta.-amino acid and optically active n-substituted .beta.-amino acid ester or optically active n-substituted 2-homopipecolic acid and optically active n-substituted 2-homopipecolic acid ester
abstract A process in which a racemic mixture of an N-substituted .szlig.-amino acid alkyl ester or N-substituted 2-homopipecolic acid ester represented by the general formula (I): (I) (wherein Ar, R1, R2, R3, R4, and R5 are as defined in the description) is subjected to selective hydrolysis of only either of the enantiomers in the presence of a hydrolase to yield an optically active, N- substituted ((R) or (S))-.szlig.-amino acid or optically active, N-substitut ed ((R) or (S))-2-homopipecolic acid represented by the general formula (II): (II) and simultaneously obtain the unreacted, optically active, N-substitute d ((S) or (R))-.szlig.-amino acid alkyl ester or unreacted, optically active, N- substituted ((S) or (R))-2-homopipecolic acid ester represented by the gener al formula (III): (III) which has the absolute configuration opposite to that o f the compound represented by the general formula (II).
priorityDate 2002-04-08-04:00^^<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: 508.