
%0 Journal Article
%A Stewart, FHC 
%T A synthesis of two-protected nonpeptide amides with the amino acid sequence of oxytocin
%J Australian Journal of Chemistry
%D 1966/12/01
%V 19
%N 12
%P 2361-2372
%K 
%R https://doi.org/10.1071/CH9662361
%U https://www.publish.csiro.au/paper/CH9662361 
%X 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. 
