Abstract
Three schemes for the synthesis of the heptapeptide 3–9 of the oxytocin sequence with different protective groups of the thiol function of the cysteine and the use of two main methods of condensation (the activated-ester method and the mixed-anhydride method) are considered.
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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. 114–121, January–February, 1993.
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Ivanov, A.K., Grigor'eva, E.É., Antonov, A.A. et al. Synthesis of the C-terminal hexa- and heptapeptide sequences of oxytocin. Chem Nat Compd 29, 97–103 (1993). https://doi.org/10.1007/BF00631032
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DOI: https://doi.org/10.1007/BF00631032