Nucleosides with 1,4-dioxane as sugar moiety

Andreas Stahl Madsen, Niels Langkjær, Jesper Wengel

Publikation: Bidrag til tidsskriftKonferenceartikelForskningpeer review

Resumé

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.

OriginalsprogEngelsk
BogserieNucleic Acids Symposium Series
Vol/bind52
Udgave nummer1
Sider (fra-til)269-270
ISSN0261-3166
DOI
StatusUdgivet - 2008
BegivenhedJoint Symposium of the 18th International Roundtable on Nucleosides, Nucleotides and Nucleic Acids and the 35th Inthernational Symposium on Nucleic Acids Chemistry - Kyoto, Japan
Varighed: 8. sep. 200812. sep. 2008

Konference

KonferenceJoint Symposium of the 18th International Roundtable on Nucleosides, Nucleotides and Nucleic Acids and the 35th Inthernational Symposium on Nucleic Acids Chemistry
LandJapan
ByKyoto
Periode08/09/200812/09/2008

Fingeraftryk

phosphoramidite

Bibliografisk note

Volumne: 52

Citer dette

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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.",
author = "Madsen, {Andreas Stahl} and Niels Langkj{\ae}r and Jesper Wengel",
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year = "2008",
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language = "English",
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Nucleosides with 1,4-dioxane as sugar moiety. / Madsen, Andreas Stahl; Langkjær, Niels ; Wengel, Jesper.

I: Nucleic Acids Symposium Series, Bind 52, Nr. 1, 2008, s. 269-270.

Publikation: Bidrag til tidsskriftKonferenceartikelForskningpeer review

TY - GEN

T1 - Nucleosides with 1,4-dioxane as sugar moiety

AU - Madsen, Andreas Stahl

AU - Langkjær, Niels

AU - Wengel, Jesper

N1 - Volumne: 52

PY - 2008

Y1 - 2008

N2 - 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.

AB - 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.

U2 - 10.1093/nass/nrn136

DO - 10.1093/nass/nrn136

M3 - Conference article

C2 - 18776357

VL - 52

SP - 269

EP - 270

JO - Nucleic Acids Symposium Series

JF - Nucleic Acids Symposium Series

SN - 0261-3166

IS - 1

ER -