Title of article
Synthesis of the first example of a nucleoside analogue bearing a 5′-deoxy-β-d-allo-septanose as a seven-membered ring sugar moiety Original Research Article
Author/Authors
Gwenaëlle Sizun، نويسنده , , David Dukhan، نويسنده , , Jean-François Griffon، نويسنده , , Ludovic Griffe، نويسنده , , Jean-Christophe Meillon، نويسنده , , Frederic Leroy ، نويسنده , , Richard Storer، نويسنده , , Jean-Pierre Sommadossi، نويسنده , , Gilles Gosselin، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2009
Pages
6
From page
448
To page
453
Abstract
The first example of a nucleoside analogue bearing a 5′-deoxy-β-d-allo-septanose as a seven-membered ring sugar moiety, namely 9-(5-deoxy-β-d-allo-septanosyl)-adenine, is reported. This compound was synthesized in 14 steps from the commercially available d-glycero-d-gulo-1,4-lactone. When evaluated in cell culture experiments against a broad range of viruses, it did not exhibit any significant antiviral effect or cytotoxicity.
Keywords
Septanose carbohydrates , Oxepane nucleosides , Antiviral evaluation , Synthesis
Journal title
Carbohydrate Research
Serial Year
2009
Journal title
Carbohydrate Research
Record number
966328
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