
%0 Journal Article
%A Stewart, FHC 
%T The synthesis of peptide derivatives related to evolidin
%J Australian Journal of Chemistry
%D 1969/12/01
%V 22
%N 12
%P 2663-2671
%K 
%R https://doi.org/10.1071/CH9692663
%U https://www.publish.csiro.au/paper/CH9692663 
%X Protected peptides with amino acid sequences present in the cyclic phytopeptide evolidin have been prepared. The synthetic work involved application of the 2,4,6-trimethylbenzyl carboxyl-protecting group. Acetyl was used to mask serine side-chain hydroxyl, and high-dilution cyclization of one of the products, an O-acetyl heptapeptide p- nitrophenyl ester, gave a low yield of O-acetylevolidin, which was converted into evolidin by hydrazinolysis. 
