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Synthesis of two phenolic amino acids containing the 1,2,4‐oxadiazole ring The synthesis of α‐amino‐β [3‐( p ‐hydroxyphenyl)‐1,2,4, oxadiazol‐5‐yl]propionic acid (9) and its β‐amino isomer (10) (see scheme 3 ) is reported. By condensation of p ‐benzyloxy‐benzamide oxime and N‐benzyloxycarbonyl asparagine the derivatives 4 and 5 (see scheme 1 ) are obtained leading after deprotection to 9 and 10 . The synthesis of N‐carboxyanhydride of 4 (6) and its corresponding amino acid (7) and amide (8) is also described.
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Moussebois et al. (1977) studied this question.
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