http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0105696-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C327-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C327-22
filingDate 1983-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57653c777634a918b7a230d273e61f3e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbe3816ac0c40f44affe45a1240b18cd
publicationDate 1984-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0105696-A1
titleOfInvention Optically active N-substituted phenylalaninols and use therefor
abstract Optically active N-substituted phenylalaninols of the formula (I):n wherein R is isopropyl, 1-ethylpropyl, cyclopentyl, cyclohexyl, cycloheptyl, 4-methylbenzyl, 4-methoxybenzyl, or 3,4-methylenedioxybenryl; and acid addition salts thereof which are useful as a resolving agent, and a process for preparing D-3-acetylthio-2-methylpropionic acid which comprises reacting DL-3-acetylthio-2-methylpropionic acid with an optically active N-substituted phenylalaninol of the formula (I) to form diastereomeric salts, subjecting the formed diastereomeric salts to a fractional crystallization from a solvent to separate the D-acid salt from the L-acid salt, and then decomposing the D-acid salt with a mineral acid to give D-3-acetylthio-2-methylpropionic acid.
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priorityDate 1982-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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