By means of the H-1 chemical shifts and the proton-proton proximities as identified in H-1 double-quantum (DO) combined rotation and multiple-pulse spectroscopy (CRAMPS) solid-state NMR correlation spectra, ribbon-like and quartet-like self-assembly can be identified for guanosine derivatives without isotopic labeling for which it was not possible to obtain single crystals suitable for diffraction. Specifically, characteristic spectral fingerprints are observed for dG(C10)(2) and dG(C3)(2) derivatives, for which quart:et-like and ribbon-like self-assembly has been unambiguously identified by N-15 refocused INADEQUATE spectra in a previous study of N-15-labeled derivatives (Pham, T. N.; et al. J. Am. Chem. Soc. 2005, 127, 16018). The NH H-1 chemical shift is observed to be higher (13-15 ppm) for ribbon-like self-assembly as compared to 10-11 ppm for a quartet-like arrangement, corresponding to a change from NH center dot center dot center dot N to NH center dot center dot center dot O intermolecular hydrogen bonding. The order of the two NH2 H-1 chemical shifts is also inverted, with the NH2 proton closest in space to the NH proton having a higher or lower H-1 chemical shift than that of the other NH2 proton for ribbon-like as opposed to quartet-like self-assembly. For the dG(C3)(2) derivative for which a single-crystal diffraction structure is available, the distinct resonances and DQ peaks are assigned by means of gauge-including projector-augmented wave (GIPAW) chemical shift calculations. In addition, N-14-H-1 correlation spectra obtained at 850 MHz under fast (60 kHz) magic-angle spinning (MAS) confirm the assignment of the NH and NH2 chemical shifts for the dG(C3)(2) derivative and allow longer range through-space N center dot center dot center dot H proximities to be identified, notably to the N7 nitrogens on the opposite hydrogen-bonding face.