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Synthesis of the N-terminal tripeptide of the oxytocin sequence

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Abstract

Two schemes for the synthesis of the hydrazide of the N-terminal tripeptide of the oxytocin sequence are considered. It is shown that the most rational is a 1 + 2 scheme.

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Literature cited

  1. L. V. Mladenova-Orlinova, L. T. Vasenkov, and Ch. P. Ivanov, Bulgarian Inventors' Certificate No. 30670, IC C07c103/52.

  2. L. Velluz, G. Amaird, and R. Heymes, FRG Patent 1059471, German Classification 12q 6/01.

  3. B. Gross and J. Meienhofer, The Peptides: Analysis, Synthesis, Biology. Vol. 4. Major Methods of Peptide Bond Formation, Academic Press, New York (1979) [Russian translation, Mir, Moscow (1983), p. 421].

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  4. O. W. Howarth and D. M. J. Lilley, Prog. NMR Spectrosc.,12, 1 (1978).

    Google Scholar 

  5. V. I. Svergun, M. B. Smirnov, A. A. Antonov, et al., Khim.-farm. Zh.,5, 92 (1981).

    Google Scholar 

  6. I. É. Zel'tser, S. P. Tikhomirova, E. P. Krysin, and M. B. Smirnov, Khim. Prir. Soedin., 381 (1985).

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All-Union Scientific-Research Institute of the Technology of Blood Substitutes and Hormone Preparations, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 116–122, January–February, 1989.

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Ivanov, A.K., Karel'skii, V.N., Krysin, E.P. et al. Synthesis of the N-terminal tripeptide of the oxytocin sequence. Chem Nat Compd 25, 103–108 (1989). https://doi.org/10.1007/BF00596712

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  • DOI: https://doi.org/10.1007/BF00596712

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