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The preparation of scaffolds 5 and 6 for the synthesis of amino acids 1 and 2 was accomplished according to the general procedure previously reported (see ref 7a), having introduced some improvements concerning the oxidation of the alcohol obtained from the condensation of N-benzylleucinol with meso-tartaric acid monoester derivative. This was carried out by Dess-Martin periodinane, that was found to be more efficient than the Swern methodology used so far because of both easier synthetic procedure and absence of epimerization at C-α of the leucine mojety.
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2142778342
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note
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3 (624 mg) in H20 (7.7 mL).
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