N -Methylamino Acids in Peptide Synthesis. II. A New Synthesis of N -Benzyloxycarbonyl, N -Methylamino Acids

  • McDermott J
  • Benoiton N
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Abstract

Reaction of N-benzyloxycarbonyl derivatives of aliphatic amino acids, and threonine, aspartic, and glutamic acids whose side-chains were protected with the t-butyl group, gave the corresponding N-methylamino acid derivatives in good yields. The methionine derivative could be obtained by using only one mol of methyl iodide. Derivatives of threonine, and aspartic and glutamic acids whose side-chains were not protected could not be methylated. Analysis of the crude products of methylation in three cases showed that they contained 0–1% of racemized material.

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McDermott, J. R., & Benoiton, N. L. (1973). N -Methylamino Acids in Peptide Synthesis. II. A New Synthesis of N -Benzyloxycarbonyl, N -Methylamino Acids. Canadian Journal of Chemistry, 51(12), 1915–1919. https://doi.org/10.1139/v73-286

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