Summary
The solid-phase synthesis of a nonatetracontapeptide corresponding to the entire amino acid sequence of Thymopoietin II is described. Use of the recently developed, base-labile, fluorenylmethyloxycarbonyl-amino acids in combination withtert-butyl based side chain protecting groups and p-alkoxybenzyl ester peptide to resin linkage enabled the synthesis to be carried out under much milder reaction conditions than previously.
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Colombo, R. A new solid-phase synthesis of thymopoietin II by a mild procedure. Experientia 37, 798–800 (1981). https://doi.org/10.1007/BF01985646
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DOI: https://doi.org/10.1007/BF01985646