
TY  - JOUR
A1  - Stewart, FHC 
T1  - The synthesis of peptide derivatives related to evolidin
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1969
VL  - 22
IS  - 12
SP  - 2663
EP  - 2671
KW  - 
UR  - https://doi.org/10.1071/CH9692663 
N2  - 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. 
ER  -

