Synthesis of 4-substituted-1,2,3-triazole carbanucleoside analogues of ribavirin via click chemistry
Identifieur interne : 000614 ( Istex/Curation ); précédent : 000613; suivant : 000615Synthesis of 4-substituted-1,2,3-triazole carbanucleoside analogues of ribavirin via click chemistry
Auteurs : Isabel Pérez-Castro [Espagne] ; Olga Caama O [Espagne] ; Franco Fernández [Espagne] ; Marcos D. García [Espagne] ; Carmen L Pez [Espagne] ; Erik De Clercq [Belgique]Source :
- Organic & Biomolecular Chemistry [ 1477-0520 ] ; 2007.
English descriptors
- Teeft :
- Alkyne, Antiviral, Aryl alkyne, Benzene, Biological evaluation, Biomol, Calcd, Cdcl3, Chem, Click chemistry, Column chromatography, Cycloaddition, Dabco, Dehydroiodination, Eluent, Eluting, Equiv, Etoac, Exch, Fractions eluting, Herpes simplex virus type, Hoch, Hrms, Hrms calcd, Identical spectroscopic features, Inhibitory activities, Mmax, Mmol, Reaction mixture, Room temperature, Royal society, Target compounds, Triazole, Virtual.
Abstract
The synthesis and biological evaluation as antiviral agents of a series of racemic 4-aryl-1,2,3-triazolo-2′,3′-dideoxy-2′-iodocarbanucleosides and 4-aryl-1,2,3-triazolo-2′,3′-dideoxy-2′,3′-didehydrocarbanucleosides is presented. These compounds were produced using a click chemistry approach, with the iodoazide 13a as the key intermediary.
Url:
DOI: 10.1039/b710348d
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<term>Benzene</term>
<term>Biological evaluation</term>
<term>Biomol</term>
<term>Calcd</term>
<term>Cdcl3</term>
<term>Chem</term>
<term>Click chemistry</term>
<term>Column chromatography</term>
<term>Cycloaddition</term>
<term>Dabco</term>
<term>Dehydroiodination</term>
<term>Eluent</term>
<term>Eluting</term>
<term>Equiv</term>
<term>Etoac</term>
<term>Exch</term>
<term>Fractions eluting</term>
<term>Herpes simplex virus type</term>
<term>Hoch</term>
<term>Hrms</term>
<term>Hrms calcd</term>
<term>Identical spectroscopic features</term>
<term>Inhibitory activities</term>
<term>Mmax</term>
<term>Mmol</term>
<term>Reaction mixture</term>
<term>Room temperature</term>
<term>Royal society</term>
<term>Target compounds</term>
<term>Triazole</term>
<term>Virtual</term>
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<front><div type="abstract">The synthesis and biological evaluation as antiviral agents of a series of racemic 4-aryl-1,2,3-triazolo-2′,3′-dideoxy-2′-iodocarbanucleosides and 4-aryl-1,2,3-triazolo-2′,3′-dideoxy-2′,3′-didehydrocarbanucleosides is presented. These compounds were produced using a click chemistry approach, with the iodoazide 13a as the key intermediary.</div>
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