Abstract
I report on the preparation of (9-β-ᴅ-ribofuranosyl)-s-triazolo-[1,2a]-purine-6-one (2) by cycli- zation of N-1-amino guanosine (1) with formamide. The tricyclic nucleoside analogue was characterized by NMR-spectroscopy (1H-NMR; 13C-NMR). The utility of 2 for the introduction of “crosslinks” in double stranded nucleic acids is discussed.
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