
%0 Journal Article
%A Abdipranoto, A 
%A Hope, AP 
%A Halpern, B 
%T The use of N<sup>&#949;</sup>-2-Hydroxyarylmethylene-protected ornithine and lysine derivatives in solid-phase peptide synthesis
%J Australian Journal of Chemistry
%D 1977/12/01
%V 30
%N 12
%P 2711-2715
%K 
%R https://doi.org/10.1071/CH9772711
%U https://www.publish.csiro.au/paper/CH9772711 
%X N&#945;-t-Butoxycarbonyl-N&#949;-(2-hydroxyarylmethylene)-ornithine and -lysine have been synthesized and coupled with amino acyl resins in the presence of dicyclohexylcarbodiimide to form N-protected peptide resin esters. The ketimine protecting group was found to be stable under anhydrous conditions and the urethane blocking group could be removed preferentially. A number of lysine- and ornithine- containing peptides have been synthesized by the solid-phase technique. 
