Reaktivität von Aminosäure-Seitenkettengruppen, II. N-Acetyl-methylamide von Threonin und Hydroxyprolin

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Abstract
The N-acetyl methylamides of L-threonine and L-hydroxyproline were synthesized as peptide models for reactivity studies. An improved synthesis of N-acetyl-L-serine-methylamide resulted in a product of higher optical rotation as described earlier.

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