The alpha-configured N7 analogue of 2'-deoxyinosine [7-(2'-deoxy-alpha
-D-ribofuranosyl)hypoxanthine, C10H12N4-O-4] shows the following struc
tural characteristics: (i) the furanose part of the molecule adopts th
e 2'-endo conformation [pseudorotation phase angle 166.4 (2)degrees];
(ii) the torsion angle chi (O4'-C1'-N7-C5) is syn [70.9 (1)degrees] wi
th the base substituent pointing away from the sugar unit; (iii) the n
ucleobases are not hydrogen bonded to each other; only sugar-base hydr
ogen bonds between adjacent molecules were detected.