Synthesis of Partially Fluorinated β-Amino Acids via Morita-Baylis-Hillman Reaction

Abstract
A convenient synthesis of fluorinated β-amino acids via Morita-Baylis-Hillman reaction is described. Hydrogenation of Morita-Baylis-Hillman adducts or cuprate addition to the double bond provides ready access to α-substituted β,β-bis(trifluoromethyl) β-amino acids.