Electrophilic substitution at C(7) of a protected 7-deaza-2′- deoxyguanosine - The 2′-deoxyribonucleoside parent analogue of queuosine

DC ElementWertSprache
dc.contributor.authorRamzaeva, N.
dc.contributor.authorRosemeyer, H.
dc.date.accessioned2021-12-23T16:30:01Z-
dc.date.available2021-12-23T16:30:01Z-
dc.date.issued2007
dc.identifier.issn14228599
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/16472-
dc.description.abstractIn this manuscript we report on the regioselective electrophilic substitution at C(7) of 7-[2-deoxy-3,5-bis-O-(2-methylpropanoyl)-β-D- erythro-pentofuranosyl]-2-(formylamino)-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine (2) - a protected precursor of 7-deaza-2′-deoxyguanosine - using N,N-dimethyl-methyleniminium iodide (Eschenmoser's salt) yielding the Mannich compound 4. © 2007 by MDPI.
dc.language.isoen
dc.publisherMDPI AG
dc.relation.ispartofMolBank
dc.subject7-deazapurine
dc.subjectEschenmoser's salt
dc.subjectMannich bases
dc.titleElectrophilic substitution at C(7) of a protected 7-deaza-2′- deoxyguanosine - The 2′-deoxyribonucleoside parent analogue of queuosine
dc.typejournal article
dc.identifier.doi10.3390/m522
dc.identifier.scopus2-s2.0-50849141928
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-50849141928&doi=10.3390%2fm522&partnerID=40&md5=dfcb3ca43233300e17f5965674551798
dc.description.volume2007
dc.description.issue1
dcterms.isPartOf.abbreviationMolBank
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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