Trifluoroacetylated amino acid esters: the stability of the derivatives of cysteine, hydroxyproline, serine, threonine and tyrosine

1965 ◽  
Vol 100 (1) ◽  
pp. 298-300 ◽  
Author(s):  
A. Darbre ◽  
K. Blau
2003 ◽  
Vol 20 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Cosimo Altomare ◽  
Giuseppe Trapani ◽  
Andrea Latrofa ◽  
Mariangela Serra ◽  
Enrico Sanna ◽  
...  

ChemInform ◽  
2005 ◽  
Vol 36 (23) ◽  
Author(s):  
N. N. Polygalova ◽  
A. G. Mikhailovskii

1964 ◽  
Vol 17 (11) ◽  
pp. 1282 ◽  
Author(s):  
B Halpern ◽  
LB James

The reaction of dimedone (5,5-dimethylcyclohexane-1,3-dione) with amino-acid "active" esters leads to optically pure enamine derivatives. The dimedone derivatives of amino acid esters could also be converted by way of their hydrazides to the corresponding azides. The thiophenyl ester and azide derivatives have been used directly for peptide synthesis. The protecting group can easily be removed from the N-protected peptides by means of aqueous bromine, with the formation of 2,2-dibromodimedone and the hydrobromide of the corresponding peptide ester.


1943 ◽  
Vol 65 (9) ◽  
pp. 1670-1674 ◽  
Author(s):  
Max Frankel ◽  
Ephraim Katchalski

2021 ◽  
Vol 31 (2) ◽  
pp. 201-203
Author(s):  
Alexey V. Nelyubin ◽  
Ilya N. Klyukin ◽  
Alexander S. Novikov ◽  
Andrey P. Zhdanov ◽  
Mikhail S. Grigoriev ◽  
...  

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