Synthesis of 1-deazaadenosine analogues of (2'->-5') ApApA

DC FieldValueLanguage
dc.contributor.authorMikhailopoulo, IA
dc.contributor.authorKalinichenko, EN
dc.contributor.authorPodkopaeva, TL
dc.contributor.authorWenzel, T
dc.contributor.authorRosemeyer, H
dc.contributor.authorSeela, F
dc.date.accessioned2021-12-23T16:13:33Z-
dc.date.available2021-12-23T16:13:33Z-
dc.date.issued1996
dc.identifier.issn15257770
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/10621-
dc.description.abstractSynthesis of (2'-->5')ApApA analogues containing 1-deazaadenosine at different positions is described (32-34). The approach used the phosphotriester methodology in solution and utilized 3'-O-benzoylated derivatives of the N-6-protected 5'-O-monomethoxytrityl-1-deazaadenosine as starting material.
dc.language.isoen
dc.publisherTAYLOR & FRANCIS INC
dc.relation.ispartofNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
dc.subject2-5A
dc.subjectBINDING
dc.subjectBiochemistry & Molecular Biology
dc.subjectBIOLOGICAL-ACTIVITY
dc.subjectCHEMICAL SYNTHESIS
dc.subjectNUCLEOSIDES
dc.subjectNUCLEOTIDES
dc.subjectPROTECTION
dc.subjectRNA
dc.subjectSOLID-PHASE
dc.titleSynthesis of 1-deazaadenosine analogues of (2'->-5') ApApA
dc.typejournal article
dc.identifier.doi10.1080/07328319608002397
dc.identifier.isiISI:A1996TV07500033
dc.description.volume15
dc.description.issue1-3
dc.description.startpage445
dc.description.endpage464
dc.contributor.orcid0000-0002-9138-9271
dc.identifier.eissn15322335
dc.publisher.place530 WALNUT STREET, STE 850, PHILADELPHIA, PA 19106 USA
dcterms.isPartOf.abbreviationNucleosides Nucleotides Nucleic Acids
crisitem.author.deptInstitut für Chemie neuer Materialien-
crisitem.author.deptidinstitute11-
crisitem.author.parentorgFB 05 - Biologie/Chemie-
crisitem.author.grandparentorgUniversität Osnabrück-
crisitem.author.netidRoHe783-
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