http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0107652-B1

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P19-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P19-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H3-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H3-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-02
filingDate 1982-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1987-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0107652-B1
titleOfInvention Preparation of 6-deoxy-d-fructose and 6-deoxy-l-sorbose
abstract 6-Deoxy-D-fructose and 6-deoxy-L-sorbose, useful starting materials for the synthesis of 4-hydroxy-2,5dimethyl-2,3-dihydrofuran-3-one, are obtained from fructose-1,6-diphosphate by a reaction with lactaldehyde, in the presence of an enzymatic system composed of aldolase and triose phosphate isomerase (TPI) in an aqueous medium at pH 7.0, followed by the hydrolysis of the monophosphate salt thus obtained. The same deoxy-sugars are obtained by the reaction between 1,3-dihydroxyacetone phosphate and lactaldehyde in the presence of the same enzymatic system composed of aldolase and TPI. The aforementioned deoxy-sugars are also prepared by the reaction of 1,3-dihydroxy-acetone with lactaldehyde in the presence of an anionic exchange resin.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8389248-B2
priorityDate 1982-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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