http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IN-2011MU03243-A

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filingDate 2011-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2015-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IN-2011MU03243-A
abstract An industrially viable method for the preparation of fludarabine phosphate; wherein debenzylation of 9-(2,3,5-tri-0-berizyl-|3-D-arabinofuranosyl)-2-fluoroadenine intermediate with palladium-charcoal in presence of transfer hydrogenating agent in an organic solvent and further purification of fuldarabine free base in cation exchange resin to pure fludarabine free base and its phosphate salt with pharmaceutically acceptable purity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105859812-B
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priorityDate 2011-11-17-04:00^^<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: 19.