Conclusions
Alkylation of alanine, phenylalanine, and glycine in the Ni(II) complexes of their Schiffs bases with S-2-N-(N′-benzylpropyl)aminobenzophenone followed by Chromatographic separation of the diastereomers has given optically pure S- and R-α-methyl-α-aminoacids.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2798–2804, December, 1987.
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Belokon', Y.N., Chernoglazova, N.I., Bakhmutov, V.I. et al. Asymmetric synthesis of α-methylaminoacids by the alkylation of glycine, alanine, and phenylalanine in chiral Ni(II) complexes. Russ Chem Bull 36, 2595–2601 (1987). https://doi.org/10.1007/BF00957242
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DOI: https://doi.org/10.1007/BF00957242