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Asymmetric synthesis of threonine and allothreonine from the D- and L-enantiomers of potassium bis-(N-salicylideneglycinato)cobaltate (III)

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    The resolution of potassium D,L-bis-(N-salicylideneglycinato)cobaltate (III) with brucine was accomplished.

  2. 2.

    The reaction of either the D- or L-forms of potassium bis-(N-salicylideneglycinato)cobaltate with acetaldehyde under the influence of bases leads to the asymmetric synthesis of threonine (45%) and allothreonine; the R-form of the amino acid predominates for the D-form of the complex, and the S-amino acid predominates for the L-form.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 156–158, January, 1973.

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Belokon', Y.N., Dolgaya, M.M., Kuznetsova, N.I. et al. Asymmetric synthesis of threonine and allothreonine from the D- and L-enantiomers of potassium bis-(N-salicylideneglycinato)cobaltate (III). Russ Chem Bull 22, 158–160 (1973). https://doi.org/10.1007/BF00854149

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  • DOI: https://doi.org/10.1007/BF00854149

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