http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1621529-A1

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filingDate 2004-03-17^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6d1bb125295059ffa0cc885b75ad712
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaec4e9530bcaa97b1c7788d3a408a66
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15c27e6c57bd47bfc886523325e00b19
publicationDate 2006-02-01^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1621529-A1
titleOfInvention 3-AMINO-3-ARYLPROPIONIC ACID n-ALKYL ESTERS, PROCESS FOR PRODUCTION THEREOF, AND PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-3-ARYLPROPIONIC ACIDS AND ESTERS OF THE ANTIPODES THERETO
abstract The present invention is to provide an n-alkyl 3-amino-3-arylpropionate represented by the formula (I):n nwherein Ar 1 represents an aryl group which may have a substituent(s), provided that a phenyl group and 4-methoxyphenyl group are excluded, R 1 represents an n-propyl group or an n-butyl group, nand a process for preparing the same, and its optically active compound and an optically active (S or R)-3-amino-3-arylpropionic acid represented by the formula (III-a):n nwherein Ar represents an aryl group which may have a substituent(s), and * represents an asymmetric carbon, nand a process for preparing an optically active n-alkyl (R or S)-3-amino-3-arylpropionate represented by the formula (IV-a):n nwherein Ar and R 1 have the same meanings as defined above, * represents an asymmetric carbon, provided that it has a reverse absolute configuration to the compound of the formula (III-a).
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