Four 3-amino-2,3,6-trideoxysugars were synthesized by a divergent route from a single enone 9a. The Migita-Stille coupling introduced a methyl group at the 3-position. Stereoselective reduction of enone and the Mitsunobu reaction provided both beta- and alpha-hydroxy groups at the 4-position. Stereospecific radical cyclization of the C4 carbamoyl moiety furnished the desired 5a, 5b and 6a, 6b, respectively.