Diastereoisomerically Pure, (<i>S</i>)-<i>O</i>-1,2-<i>O</i>-isopropyli dene-(5-<i>O</i>-α-<span style="font-variant: small-caps">d</span>-glucofuranosyl) <i>t</i>-butanesulfinate: Synthesis, Crystal Structure, Absolute Configuration and Reactivity

Abstract

The reaction of t-butylmagnesium chlorides with diastereomerically pure (R)-1,2-O-isopropylidene-3,5-O-sulfinyl-α-d-glucofuranose (R)-4 was found to be stopped at the stage of the corresponding, diastereoisomerically pure 1,2-O-isopropylidene-(5-O-α-d-glucofuranosyl) t-butanesulfinate (S)-10 for which the crystal structure and the (S)-absolute configuration was determined by X-ray crystallography. Comparison of the absolute configurations of the starting sulfite (R)-4, and t-butanesulfinate (S)-10 (which crystallizes in the orthorhombic system, space group P212121, with the single compound molecule present in the asymmetric unit), clearly indicates that the reaction of nucleophilic substitution at the stereogenic sulfur atom in the sulfite (R)-4 occurs with the full inversion of configuration via the trigonal bipyramidal sulfurane intermediate 4c in which both the entering and leaving groups are located in apical positions.

Keywords

• diastereoisomeric sulfites and sulfinates
• sulfinylation
• crystal structure
• X-ray crystallography
• single-crystal diffractometry
• absolute configuration