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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-007
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filingDate 1963-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1061717-A
titleOfInvention A process for the preparation of water-insoluble derivatives of acylase
abstract A water insoluble derivative of acylase (see Division C3) is used to cause asymmetric hydrolysis and optical resolution of N-acyl-DL-amino acids to produce optically active amino acids. Examples relate to the production of L-valine and L-alanine from the N-acetyl derivatives of the DL acids. Other acids mentioned are leucine, glutamic acid, methionine, phenylalanine (all in N-acetyl form) and lysine (in e -N-benzoyl-a -N-acetyl form).ALSO:A water-insoluble acylase derivative is produced by reacting acylase with an N-carboxy-a -amino anhydride and/or an N-carboxy-a -amino anhydride having a second carboxylic acid group (not adjacent to the amino group) which may be esterified. Specified reactants are the N - carboxy - a - amino acid anhydrides of a - amino n - butyric acid, valine, leucine, isoleucine, phenyl alanine, a b -methyl-, ethyl- or benzyl-ester of aspartic acid or a g -ester of glutamic acid. Co+ + +, Ca+ + or Zn+ + ions or cysteine may be present as an acylase inactivator. The product is useful in resolving DL amino acids by asymmetric hydrolysis (see Division C2).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4224411-A
priorityDate 1962-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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