aspartyl peptides
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2001 ◽  
Vol 42 (43) ◽  
pp. 7703-7705 ◽  
Author(s):  
Vassiliki Theodorou-Kassioumis ◽  
Nikolaos Biris ◽  
Constantinos Sakarellos ◽  
Vassilios Tsikaris

1998 ◽  
Vol 273 (41) ◽  
pp. 26295-26297 ◽  
Author(s):  
Tiina Noronkoski ◽  
Ivanka B. Stoineva ◽  
Ivailo P. Ivanov ◽  
Dimiter D. Petkov ◽  
Ilkka Mononen

Neuropeptides ◽  
1994 ◽  
Vol 27 (1) ◽  
pp. 19-26 ◽  
Author(s):  
V Varga ◽  
R Janáky ◽  
P Saransaari ◽  
S.S Oja
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1989 ◽  
Vol 54 (12) ◽  
pp. 3360-3373 ◽  
Author(s):  
István Schön ◽  
Attila Rill

Ammonolysis of Z-Asp(OBut)-Phe-NH2 and Boc-Leu-Asp(OBut)-Phe-NH2, as well as their diastereomers, resulted not only in transpeptidated, but also in epimerized peptides through a complex mechanism. Key compounds of these transformations are presumably very reactive cyclic aminosuccinyl derivatives. In some cases, the amount of α-peptide formed approached that of the β-peptide, in one case it exceeded this amount.


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