http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2726513-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_04ca390052b363bf3f6c288d9ed7fc1d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-18
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-727
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-10
filingDate 2012-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0bb969e00a860d664d7b57ee70a521d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_605c76bb023b1b341e1d80e77da51f8c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c6cba0b640e4b03f209fab479a16dba
publicationDate 2014-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2726513-A1
titleOfInvention Process for preparing heparinoids and intermediates useful in the synthesis thereof
abstract Processes are disclosed for the synthesis of the Factor Xa anticoagulant fondaparinux and related compounds. Protected pentasaccharide intermediates and efficient and scalable processes for the industrial scale production of fondaparinux sodium by conversion of the protected pentasaccharide intermediates via a sequence of deprotection and sulfonation reactions are provided.
priorityDate 2011-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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