http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002226472-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-60
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-60
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-66
filingDate 2002-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9765b2e5b63659f7afebf215edf27331
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a37f2a86f2f82b729d273deab5001b5
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_711327949218c3781b36c75120139995
publicationDate 2002-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002226472-A
titleOfInvention Amino- and hydroxyfuranones enriched in one enantiomer
abstract (57) [Problem] To provide an optically active aminofuranone and hydroxyfuranone which are enriched in one enantiomer in a high yield and without racemization. SOLUTION: One enantiomer-rich cyanohydrin is acylated with an acylating agent and then cyclized at 40-90 ° C in the presence of zinc or a zinc compound to give one enantiomer-rich corresponding amino acid. A process for preparing one enantiomer-rich aminofuranone and hydroxyfuranone, which is converted to the corresponding enantiomer-rich hydroxyfuranone, which is furanone, and optionally by acid hydrolysis, if necessary.
priorityDate 2001-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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