Chemistry of Natural Compounds

, Volume 28, Issue 3–4, pp 344–349 | Cite as

Synthesis of the amide of the C-terminal tetrapeptide of the sequence of oxytocin

  • A. K. Ivanov
  • A. A. Antonov
  • I. A. Donetskii
Article
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Abstract

The synthesis has been effected of the amide of the tetrapeptide forming the sequence 6–9 of oxytocin with the use of benzyl protection of the thiol function of cysteine by two main schemes 1+3 and 2+2. The advantageousness of performing the synthesis by the 2+2 scheme has been shown. The overall yield of tetrapeptide using the method of condensation with the formation of mixed anhydrides amounted to 51% by the scheme proposed.

Keywords

Organic Chemistry Amide Cysteine Thiol Anhydride 

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Literature cited

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    Zh. D. Bespalova et al., Khim. Prir. Soedin., 808 (1973); Zh. D. Bespalova et al., Zh. Obshch. Khim.,44, No. 1 (1973).Google Scholar
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    S. Ya. Miksta et al., Izv. Akad. Nauk, LatvSSR, Ser. Khim., No. 5, 618–621 (1975).Google Scholar

Copyright information

© Plenum Publishing Corporation 1992

Authors and Affiliations

  • A. K. Ivanov
  • A. A. Antonov
  • I. A. Donetskii

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