
TY  - JOUR
A1  - Hope, AP 
A1  - Halpern, B 
T1  - The application of ketimine derivatives of amino acids to peptide synthesis
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1976
VL  - 29
IS  - 7
SP  - 1591
EP  - 1603
KW  - 
UR  - https://doi.org/10.1071/CH9761591 
N2  - N-(2-Hydroxyarylmethy1ene)amino acids have been coupled with amino acid esters to form sterically pure N-protected dipeptide esters. The protecting group can be removed by means of 80% acetic acid under conditions which leaves the t-butyloxycarbonyl protecting group intact. Biologically active peptides which are C-terminal partial sequences of substance P were prepared and were shown to have the expected vasodilator, spasmogenic and venoconstrictor properties. 
ER  -

