http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7781609-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-60
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filingDate 2006-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1988883318ee24592a78821daf24630c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f8a81169781c8a232729491138c5a79
publicationDate 2010-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7781609-B2
titleOfInvention Process for producing optically active β-hydroxy-α-aminocarboxylic acid derivative
abstract There is provided a process for efficiently producing an anti form of an optically active β-hydroxy-α-aminocarboxylic acid derivative that is useful as an intermediate for pharmaceuticals and agrochemicals. The process for producing optically active β-hydroxy-α-aminocarboxylic acid derivative of formula (2) or (3) n ntherein R 1 is substituted or unsubstituted C 1-20 alkyl group, or substituted or unsubstituted C 4-12 aromatic group, R 2 is substituted or unsubstituted C 1-20 alkyl group, or substituted or unsubstituted C 4-12 aromatic group, comprising subjecting an α-aminoacyl acetic acid ester compound of formula (1)n n nwherein R 1 and R 2 have the same meaning as the above, to hydrogenation by catalytic asymmetric hydrogenation in the presence of an acid by using as a catalyst a rhodium complex containing as a ligand an optically active compound of formula (4), (4′) or (5)n n ncharacterized in that the hydrogenation is conducted in the presence of an acetic acid salt.
priorityDate 2005-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 567.