http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2907629-T3

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filingDate 2016-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae98450b0132da1f21cc75baa1be967d
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publicationDate 2022-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2907629-T3
titleOfInvention A method for preparing a substantially diastereomerically pure phosphorodiamidate oligomer, a phosphorodiamidate oligomer prepared by said method and a pharmaceutical composition comprising said phosphorodiamidate oligomer
abstract A method for preparing a diastereomerically pure substantially phosphorodiamidate morpholino oligomer comprising chiral phosphorous bonds, comprising: selecting substantially stereochemically pure phosphoramidochloridate morpholino monomers; and synthesizing a diastereomerically pure substantially pure phosphorodiamidate morpholino oligomer by stereospecific coupling of selected stereochemically substantially pure phosphoramidochloridate morpholino monomers, wherein said stereospecific coupling is performed in an aprotic solvent, in the presence of a non-nucleophilic tertiary amine or aromatic base , at a temperature of 20 °C to 50 °C; wherein substantially stereochemically pure phosphoramidochloridate morpholino monomers are obtained by separating a diastereoisomeric mixture of phosphoramidochloridate morpholino monomers into substantially stereochemically pure phosphoramidochloridate monomers, and wherein substantially stereochemically pure indicates enantiomers or diastereomers that are in enantiomeric or diastereomeric excess , respectively, equal to or greater than 87%, and "substantially diastereomerically pure" indicates diastereoisomers that are in diastereomeric excess equal to or greater than 87%.
priorityDate 2015-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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