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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_83dad3f7dc254b88fdca525a50124d81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_52c9ec051450ed982e33c7e431a3516c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H3-02
filingDate 1985-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48a75b9be13a09cedc95120524a802a8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42a028335e346fc11509b4d528f17443
publicationDate 1987-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-251992-B1
titleOfInvention A method of preparing 1,6-anhydro-2,3-di-O-acetyl- (β-D-glucopyranose)
abstract The process addresses the method of stereospecific preparationnl, 6-anhydrides <JRO-2,3-di-O-acetyl (3-D-glucopyranose.nIt will achieve this purposenin that 1,6-anhydro-2,3,4-tri-O-acetyl- (S-n-D-glucopyraposis is catalytically caused by cellsnAureobasidium pullulansccy 27-1-14 vnbuffer of pH 5.0 to 5.8, whereinna suitable buffer is phosphate citratenor malate-phosphate.nThe solution is important in chemistry and biochemistryncarbohydrates.
priorityDate 1985-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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