
TY  - JOUR
A1  - Abdipranoto, A 
A1  - Hope, AP 
A1  - Halpern, B 
T1  - The use of N<sup>&#949;</sup>-2-Hydroxyarylmethylene-protected ornithine and lysine derivatives in solid-phase peptide synthesis
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1977
VL  - 30
IS  - 12
SP  - 2711
EP  - 2715
KW  - 
UR  - https://doi.org/10.1071/CH9772711 
N2  - 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. 
ER  -

