http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6075497-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c999fee6428152a996011d506925c2d7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-0613
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-02
filingDate 1983-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a39fe241207af2ed6367b6266c3a6b1a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65140a4d557438a45264b7b99f3a469c
publicationDate 1985-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6075497-A
titleOfInvention Production of n-protected-alpha-l-aspartyl-l-phenylalanine methyl ester
abstract PURPOSE: L-phenylalanine methyl ester is allowed to react with fine particles of N-carbobenzoxy-L-aspargic anhydride to achieve high-yield production of the α- isometer of the titled compound which is used as a sweetener with inhibition of β-isomer formation. n CONSTITUTION: The reaction of (A) L-phenylalanine methyl ester with (B) fine particles, preferablyless than 50 micron particle size, of N-carbobenzoxy-L- aspargic anhydride, is carried out, preferably at a molar ratio of 0.8W1.2, usually in an inert solvent such as acetic acie or toluene, preferably at a temperature lower than 80°C to give the objective compound. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1983-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 22.