Pyrimidine acyclo-C-nucleosides by ring transformations of 2-formyl-L-arabinal

dc.bibliographicCitation.firstPage837eng
dc.bibliographicCitation.issue8eng
dc.bibliographicCitation.journalTitleMoleculeseng
dc.bibliographicCitation.volume10eng
dc.contributor.authorBari, A.
dc.contributor.authorFeist, H.
dc.contributor.authorMichalik, M.
dc.contributor.authorPeseke, K.
dc.date.accessioned2020-08-07T13:48:29Z
dc.date.available2020-08-07T13:48:29Z
dc.date.issued2005
dc.description.abstractThe protected 2-formyl-L-arabinal 2 reacted with thiourea and cyanamide in the presence of sodium hydride to afford via ring transformations the 5-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl]-1,2-dihydropyrimidines 3 and 4, respectively. Similarly, treatment of 2 with 3-amino-2H-1,2,4-triazole yielded 6-[1R,25-1,2-bis(benzyloxy)-3-hydroxypropyl][1,2,4]-triazolo[1,5-a]pyrimidine(5) .eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/4006
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/5377
dc.language.isoengeng
dc.publisherBasel : MDPIeng
dc.relation.doihttps://doi.org/10.3390/10080837
dc.relation.issn1420-3049
dc.rights.licenseCC BY-NC-SA 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/3.0/eng
dc.subject.ddc540eng
dc.subject.otherFused pyrimidineseng
dc.subject.otherGlycalseng
dc.subject.otherNucleoside analogueseng
dc.subject.otherPush-pull alkeneseng
dc.subject.otherPyrimidineseng
dc.subject.otherRing transformationeng
dc.subject.other3,4 di O benzyl 2 formylarabinaleng
dc.subject.other3,4-di-O-benzyl-2-formylarabinaleng
dc.subject.otherarabinoseeng
dc.subject.otherdrug derivativeeng
dc.subject.otherpyrimidine nucleosideeng
dc.subject.otherarticleeng
dc.subject.otherchemistryeng
dc.subject.othernuclear magnetic resonance spectroscopyeng
dc.subject.othersynthesiseng
dc.subject.otherArabinoseeng
dc.subject.otherMagnetic Resonance Spectroscopyeng
dc.subject.otherPyrimidine Nucleosideseng
dc.titlePyrimidine acyclo-C-nucleosides by ring transformations of 2-formyl-L-arabinaleng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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