(1-13C)alditols: elimination of magnetic equivalence in 1H- and 13C-n.m.r. spectra of symmetric compounds through (13C)-substitution.

Article abstract of DOI:10.1016/0008-6215(90)80082-E

(1-13C)Glycerol, D-(1-13C)arabinitol, D-(1-13C)ribitol, D-(1-13C)xylitol, D-(1-13C)glucitol, D-(1-13C)mannitol, and D-(1-13C)talitol have been prepared by NaBH4 reduction of the corresponding (1-13C)aldoses. A comparison of the 1H- (300 and 620 MHz) and 13C (75 MHz) n.m.r. spectra of natural and (1-13C)-substituted dissymmetric alditols has permitted the unequivocal assignments of their hydroxymethyl proton and carbon signals and the measurement of several 13C-1H and 13C-13C spin-coupling constants. Similar spectra of (1-13C)-substituted symmetric alditols, however, are more difficult to interpret since they are composed of overlapping 13C-coupled and 13C-noncoupled subspectra. In some cases, 1H difference spectra and 1H-coupled 13C spectra may be used to extract the 13C-1H and 13C-13C spin couplings from the 13C-coupled component. These couplings have been examined in light of conformational models previously proposed, permitting a preliminary evaluation of standard 3JCH and 3JCC values for specific coupling pathways in these compounds.