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Article: Synthesis and stability of exocyclic triazine nucleosides

TitleSynthesis and stability of exocyclic triazine nucleosides
Authors
Issue Date2005
Citation
Organic and Biomolecular Chemistry, 2005, v. 3, n. 16, p. 2946-2952 How to Cite?
AbstractSynthesis and stability studies of exocyclic amino triazine nucleosides were performed. Stability of the nucleosides was found to be dependent on triazine ring electron density, solvent, and pH. The nucleosides were found to be more stable when the triazine ring was electron deficient, in high pH aqueous solutions and in aprotic solvents. © The Royal Society of Chemistry 2005.
Persistent Identifierhttp://hdl.handle.net/10722/341076
ISSN
2023 Impact Factor: 2.9
2023 SCImago Journal Rankings: 0.607
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHysell, Michelle-
dc.contributor.authorSiegel, Jay S.-
dc.contributor.authorTor, Yitzhak-
dc.date.accessioned2024-03-13T08:39:58Z-
dc.date.available2024-03-13T08:39:58Z-
dc.date.issued2005-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2005, v. 3, n. 16, p. 2946-2952-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10722/341076-
dc.description.abstractSynthesis and stability studies of exocyclic amino triazine nucleosides were performed. Stability of the nucleosides was found to be dependent on triazine ring electron density, solvent, and pH. The nucleosides were found to be more stable when the triazine ring was electron deficient, in high pH aqueous solutions and in aprotic solvents. © The Royal Society of Chemistry 2005.-
dc.languageeng-
dc.relation.ispartofOrganic and Biomolecular Chemistry-
dc.titleSynthesis and stability of exocyclic triazine nucleosides-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b503757c-
dc.identifier.pmid16186926-
dc.identifier.scopuseid_2-s2.0-24144445624-
dc.identifier.volume3-
dc.identifier.issue16-
dc.identifier.spage2946-
dc.identifier.epage2952-
dc.identifier.isiWOS:000230964400010-

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