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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-697
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filingDate 2003-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c4dd0383f1be61b1d94341307946a78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d64f8ed941b298416ae09003bd79cb76
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publicationDate 2005-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20050536-A1
titleOfInvention A PROCEDURE FOR THE PREPARATION OF OPTICALLY PURE OR ENRICHED RACEMIC TETRALONE
abstract IT REFERS TO A CHROMATOGRAPHIC PROCEDURE TO OBTAIN OPTICALLY PURE CHIRAL TETRALONE AS AN INTERMEDIATE PRODUCT IN THE PREPARATION OF OPTICALLY PURE SERTRALINE FROM A MIXTURE OF TWO TRETALONE ENANTHYOMERS THAT INCLUDES: a) UNDERSTANDING THE UNDERSTANDED MOVEMENT OF LEFT; b) THE PROVISION OF A STATIONARY CHIRAL PHASE THAT INCLUDES AN INORGANIC CARRIER THAT HAS AN OPTICALLY PURE METALLIC-ORGANIC COMPLEX AND c) THE CHROMATOGRAPHIC SEPARATION OF THE MIXTURE TO OBTAIN AT LEAST ONE TETRALONE SUBSTANTIAL ORGANIC SIMPLE ORGANIC ENANTIOGRAPHIC ENANTIOMURA UTILIZING TETRALONE IN PURPOSE AND ENANTIOMY COLUMATURE, UTILIZING PICTURE AND ENANTIOMURE KEEP GOING . THE SOLVENT IS SELECTED FROM METHANOL, ETHANOL, PROPANOL, ISOPROPANOL, BUTANOL, AMONG OTHERS. THE MIXTURE IS CARRIED OUT AT A TEMPERATURE BETWEEN 40 ° C AND 80 ° C AND THE CATIONS THAT FORM A COMPLEX ARE SELECTED FROM NICKEL, OSMIUM, RUTHENIUM, PLATINUM, IRON AMONG OTHERS. THE STATIONARY CHIRAL PHASE HAS A PARTICLE SIZE BETWEEN 5 AND 30 um. THE PROCEDURE IS CHARACTERIZED BECAUSE THE METALLIC-ORGANIC COMPLEX HAVE AN ORGANIC LIGAND WHICH IS A HETERO CYCLE THAT GIVES IT CHIRALITY AND THE LIGAND IS SELECTED FROM 2,2-DIPYRIDINE, 1,10-PHENANTHROLINE
priorityDate 2003-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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