Glaxo Laboratories Limited

Joseph Elks

Niall Galbraith Weir

John Colin Clark

Brian Burton

Timothy Larry Gane

A process for the production of an ester of one enantiomer of an .alpha.-amino acid in the form of a salt with an optically active acid, which comprises reacting an ester of the opposite enantiomer of said .alpha.-amino acid (which may be in admixture with an ester of the desired enantiomer) with said optically active acid and an aldehyde or ketone, whereby an ester of the desired enantiomer separates out in the form of the said salt. The free .alpha.-amino acid and/or its salts may be obtained by hydrolysis of the ester thus formed.

Production of an ester of one enantiomer of an .alpha.-amino acid in the

D(-)-Penicillamine and salts thereof may be prepared by reacting a 6-amino or blocked 6-amino penicillin e.g. penicillin G or penicillin V, or a salt thereof, with a hydrazine having two --NH-groups, or a salt or solvate thereof.

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London, United Kingdom

Joseph Elks