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Synthesis of diastereomers of sarcolysylleucine

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

Conclusions

  1. 1.

    The diastereomers of sarcolysylleucine with a formylated and free amino group in sarcolysine residue were obtained by using the N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline method to form the peptide linkage.

  2. 2.

    The possibility of deformylating peptides, containing the di-2-chloroethyl group, by hydrazine acetate was studied.

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Literature cited

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 717–719, March, 1978.

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Karpavichyus, K.I., Klyukene, R.B. & Kil'disheva, O.V. Synthesis of diastereomers of sarcolysylleucine. Russ Chem Bull 27, 622–624 (1978). https://doi.org/10.1007/BF00923961

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  • DOI: https://doi.org/10.1007/BF00923961

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