Two straightforward strategies for the synthesis of thiodisaccharides with a furanose unit as the nonreducing end
Thiodisaccharides having a 1-thiopentofuranose nonreducing end were synthesized by two routes starting from per-O-acylaldofuranoses with arabino, ribo, and xylo configurations. These glycosyl donors were converted into S-glycosyl isothiourea derivatives as precursors of 1-thiofuranose units, which w...
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| Autores principales: | Repetto, E., Marino, C., Uhrig, M.L., Varela, O. |
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| Formato: | JOUR |
| Materias: | |
| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_1434193X_v_n3_p540_Repetto |
| Aporte de: |
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