http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-185960-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38
filingDate 1981-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6228562f9a1c579589d61ad893fae12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f330c920737fd54023e55168b8e3bbf
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publicationDate 1985-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-185960-B
titleOfInvention Process for producing optically active alpha-aminophosphonic acids and optically active n-acyl-alpha-aminophosphonic acids
abstract The present invention relates to optically active α-aminophosphonic acids of formula (I) and optically active N-acyl-α-aminophosphonic acids, wherein R 1 is C 1 -C 6 straight chain alkyl optionally substituted with phenyl or phenyl. ; R2 is C1-C4 alkyl optionally substituted by halogen. According to the method, a racemic N-acyl-α-aminophosphonic acid of formula (II) is resolved in an aqueous medium at pH 6-8 with an aminoacylase enzyme, and the deacylated La-aminophosphonic acid enantiomer is separated into the unaltered DN-eye. foszfonsavtól. This compound is desacylated if desired. If necessary, L-α-aminophosphonic acid is converted to L-Nacyl-α-aminophosphonic acid by acid chloride or acid anhydride. As an appropriate solution, the aminoacylase is used in an immobilized form. The advantage of the process is that the resolving agent is a non-costly, stable formulation with high yield, high-purity end-product. I II / OH R, -C-P I • OH NH 2 H 0 'I / OH NH OH o = c-r 2 (ii) -1-
priorityDate 1981-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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