- The stereoselective oxy-Michael addition of the 'naked' anion of (5)-6-methyl tetrahydropyran-2-ol to α-nitro-α,β-unsaturated esters followed by reduction and in situ protection of the corresponding amine provides a new and efficient route to protected β-aryl-β-hydroxy- α-amino acids. © Georg Thieme Verlag Stuttgart.
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A stereoselective oxy-Michael route to protected beta-aryl-beta-hydroxy-alpha-amino acids
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