Multigram-Scale Synthesis of 2,5-Dideoxy-2,5-imino-<scp>d</scp>-mannitol (DMDP) and 2,5-Dideoxy-2,5-imino-<scp>d</scp>-glucitol (DGDP) from <scp>d</scp>-Fructose and <scp>l</scp>-Sorbose Using a Regioselective Appel Reaction

We report a practical 5 g scale stereoselective synthesis of the valuable iminosugar DMDP from d-fructose in only 7 synthetic steps and in a 70% overall yield, which doubles previously reported yields. This process requires only two chromatographic purification steps, taking advantage of a regioselective Appel reaction. The regioselective reaction has also been applied on a similar scale to prepare the C-2 diastereomer of DMDP, DGDP, from l-sorbose in 7 steps (two purifications) and 56% overall yield, albeit with diminished diastereomeric purity (d.r. 90:10). The C-5 regioselectivity has also been illustrated on d-psicose and d-tagatose, making this an attractive method for preparing pyrrolidine iminosugars or 5-thiosugars from ketopyranoses.