Asymmetric syntheses of optically active α-amino acids by hydrocyanic acid addition to the optically active Schiff base

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Abstract
The syntheses of L(+) and D(−) enantiomers of α-amino acids, norvaline, norleucine, and leucine, as their hydrochloride salts have been achieved in almost 100% optical purity and 40–60% overall yield.

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