Carbohydrate Research p. 93 - 104 (1997)
Update date:2022-08-30
Topics:
Sallam, Mohammed A. E.
Ibrahim, El-Sayed I.
El-Eter, Khaled A.A.
Cassady, John M.
Anomeric 2-(α- and β-D-erythrofuranosyl)benzimidazole C-nucleoside analogues 2 and 3, were prepared from the corresponding epimeric 2-(D-arabino, and D-ribo-tetritol-1-yl)-benzimidazole analogues 1 and 4, respectively. Similarly, 2-(β-L-erythrofuranosyl)benzimidazole 13 was obtained from the precursor 2-(L-arabino-tetritol-1-yl)benzimidazole 12. The structure and anomeric configuration of the C-nucleoside analogues 2, 3, and 13 were determined by acylation, 1H and 13C NMR spectroscopy, and mass spectrometry.
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