The preparation of four stereoisomers of β-hydroxytyrosine containing burkholdines is described. Enantio-pure syn β-hydroxytyrosine was synthesized using Sharpless aminohydroxylation. To obtain anti β-hydroxytyrosine, the cinnamate derivative was oxidized to give the optical active diol derivative by the AD-mix and subsequently, the α-hydroxy group was converted to amine. Deprotection of the acid-sensitive β-hydroxytyrosine derivatives was successively accomplished by brief immersion in 4N HCl/dioxane. All prepared stereoisomers of β-hydroxytyrosine were available for solid and solution phase peptide synthesis and amino acid analysis.
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(2R,3R)-14 was synthesized from 13 by using AD-mix α.
