Substituted ajoenes as novel anti-cancer agents

A new synthesis of the ajoene pharmacophore core is presented involving the regioselective radical addition of a thiyl radical to a terminal alkyne as the key step. The synthesis allows structural variation of the two end groups on sulfur, and a range of novel derivatives varying the R 1 group (sulf...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2008-10, Vol.18 (19), p.5277-5279
Hauptverfasser: Hunter, Roger, Kaschula, Catherine H., Parker, Iqbal M., Caira, Mino R., Richards, Philip, Travis, Susan, Taute, Francois, Qwebani, Thozama
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Sprache:eng
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