A synthesis of two-protected nonpeptide amides with the amino acid sequence of oxytocin

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Abstract
Two protected nonapeptide amides with the amino acid sequence of oxytocin have been synthesized by a route involving the use of benzyloxycarbonyl peptide p-nitrophenyl esters as coupling components. One of the products is a compound which has been described previously, and converted into oxytocin, by various authors. The present approach is discussed in relation to the earlier syntheses.

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