The stereoselective synthesis of deoxy C‐glycoside derivatives that have a methylene or methyl group at C‐2 position was investigated by employing the Claisen rearrangement of 2‐vinyloxy methyldeoxy‐glycals as the synthetic precursors. The method proceeded with high diastereoselectivity to afford C‐2‐methylene α‐C‐glycosides. Complementary to this protocol, a ZnII‐mediated anomerization of the α‐C‐glycosides to give the corresponding β‐C‐glycosides was also used to obtain diastereomerically pure C‐2‐methylene β‐C‐glycosides. The generality of the reaction was fully evaluated, and the developed method was successfully applied to the formal stereoselective total synthesis of (–)‐brevisamide, a monocyclic ether alkaloid that was isolated from Karenia brevis (red tide dinoflagellate).