A short highly stereoselective synthesis of the fluorinated natural product (2S,3S)-4-fluorothreonine

Abstract
A three step stereoselective route to the fluorinated natural product (2S,3S)-4-fluorothreonine is described; the route is amenable to the preparation of (2S,3S)-4-fluoro[3- 2 H]threonine and (2S,3R)-[4,4,4- 2 H 3 ]threonine.

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