The origin of the anomeric effect: conformational analysis of 2-methoxy-1,3-dimethylhexahydropyrimidine

The anomeric effect is thought to be the result of either molecular orbital interactions, which stabilize the axial conformer, or electrostatic interactions, which destabilize the equatorial. To test which of these is more important, it is proposed to determine the change in the anomeric effect on replacing the oxygen of an anomeric molecule by nitrogen. Nitrogen is less electronegative than oxygen, leading to weaker electrostatic interactions and stronger molecular orbital interactions, so the two interactions act in opposite directions. Accordingly, the conformational equilibrium of 2-methoxy-1,3-dimethylhexahydropyrimidine (3) was measured by 1 H and 13 C NMR. The proportion of axial conformer is almost the same as in 2-methoxy-1,3-dioxane