The 2'-deoxyribose conformations in four natural dinucleotides, TpX (where
X is T, dC, dA or dG), dissolved in D2O, CD3OD and DMSO-d(6) were investiga
ted by H-1 NMR spectroscopy. Accurate chemical shifts and coupling constant
s derived by simulation of 1H spectra are reported. Sugar pucker parameters
derived from vicinal coupling constants are also presented. It is noted th
at there is no simple relation between sugar conformations and solvent prop
erties. Copyright (C) 2001 John Wiley & Sons, Ltd.