Nucleosides with 1,4-dioxane as sugar moiety

Abstract A synthetic route towards novel nucleosides with 1,4- dioxane as the sugar moiety has been developed. The dioxane moiety features a second anomeric center, which has been phosphitylated giving a diastereomeric mixture of the corresponding phosphoramidites.

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Veröffentlicht in:Nucleic Acids Symposium Series 2008, Vol.52 (1), p.269-270
Hauptverfasser: Madsen, Andreas Stahl, Langkjær, Niels, Wengel, Jesper
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract A synthetic route towards novel nucleosides with 1,4- dioxane as the sugar moiety has been developed. The dioxane moiety features a second anomeric center, which has been phosphitylated giving a diastereomeric mixture of the corresponding phosphoramidites.
ISSN:0261-3166
1746-8272
DOI:10.1093/nass/nrn136