http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8600323-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_26da3723d11a0786897640eceb4d464f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H5-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D421-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D421-04
filingDate 1983-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1985-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8600323-A1
titleOfInvention A PROCEDURE FOR OBTAINING 2- (2,3,5-TRI-O-ARIL-B-D-RIBOFURANOSIL) SELENAZOL-4-ALCOHYL OR ARALCOHYL CARBOXYLATES
abstract PROCEDURE TO OBTAIN 2- (2,3,5-TRI-O-ACIL-BBB-D-RIBOFURANOSIL) SELENAZOL-4-CARBOXYLATES FROM ALCOHYL OR ARALCOHYL, INCLUDING CYCLISAR 2,5-ANHYDRO-3,4,6-TRI- O-ACIL-D-ALONSELENOCARBOXAMIDE FROM THE STRUCTURE OF FORMULA (I) WHERE Z IS -C (NH2) SE, WITH AN ALCOHYL BROMOPYRUVATE OR ARALCOHYL, CARRYING OUT THE COLD REACTION IN A SUITABLE ALCOHOL OR ACETONE SOLVENT OF LOW BOILING POINT, TO OBTAIN 2- (2,3,5-TRI-O-ACIL-BBB-D-RIBOFURANOSIL) SELENAZOL-4-CARBOXYLATES OF ALCOHYL OR ARALCOHYL FROM THE STRUCTURE OF FORMULA (I), WHERE R1 , R2 AND R3 ARE EACH OF THEM AN ACILO GROUP AND Z IS A SELENAZOL-4- (ALCOHIL OR ARALCOHYL) CARBOXYLATE-2-ILO GROUP. THEY HAVE PHARMACEUTICAL APPLICATIONS FOR THEIR ANTI-TUMOR AND ANTIVIRAL ACTIVITY.
priorityDate 1982-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421037544
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID100665

Total number of triples: 17.