Title of article :
A new synthetic approach to 2,3-dideoxy-2-fluoro-β-d-threo-pentofuranose, the fluorofuranose unit of the anti-HIV-active nucleoside, β-FddA
Author/Authors :
Caille، نويسنده , , Jean-Claude and Miel، نويسنده , , Hugues and Armstrong، نويسنده , , Paul and McKervey، نويسنده , , M.Anthony، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
3
From page :
863
To page :
865
Abstract :
The fluorinated furanose unit of the anti-HIV-active nucleoside (2,3-dideoxy-2-fluoro-β-d-threo-pentofuranosyl)adenine, β-FddA, has been synthesized as its 5-trityl derivative with high stereocontrol from (S)-trityl glycidol and phenylthioacetic acid.
Keywords :
phenylthioacetic acid , Stereospecific fluorination , Anti-viral , Fluorofuranose , Epoxide ring opening
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1656729
Link To Document :
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