Synthesis of Selectively Protected Homoserine and α,γ-Diaminobutyric Acid Derivatives1

1961 ◽  
Vol 26 (5) ◽  
pp. 1482-1487 ◽  
Author(s):  
T. SHERADSKY ◽  
Y. KNOBLER ◽  
MAX FRANKEL
Keyword(s):  
Author(s):  
Ramoncito Luis B. Boda ◽  
Carl Angelo M. Caluag ◽  
Rachelle Anne S. Dante ◽  
Art Gersun J. Petate ◽  
Hermie Patrice T. Candaza ◽  
...  

2020 ◽  
Vol 191 ◽  
pp. 110247 ◽  
Author(s):  
Xiaofang Luo ◽  
Shumin Zhu ◽  
Jue Wang ◽  
Julong Sun ◽  
Lingjun Bu ◽  
...  

1969 ◽  
Vol 22 (5) ◽  
pp. 207-210 ◽  
Author(s):  
W. K. HAUSMANN ◽  
D. B. BORDERS ◽  
J. E. LANCASTER
Keyword(s):  

1994 ◽  
Vol 49 (1-2) ◽  
pp. 18-25 ◽  
Author(s):  
G. Filsak ◽  
K. Taraz ◽  
H. Budzikiewicz

Condensation of 2,4-diaminobutyric acid (Dab) with other amino acids yields tetrahydropyrimidine derivatives. Such condensation products can be constituents of the peptide chain of pyoverdins and ferribactins (the siderophors of fluorescent pseudomonads). Synthesis of several representatives and model substances allows to confirm earlier structural conclusions based mainly on NMR evidence. Apparent anomalies accompanying the derivatization for GC/MS analysis could be clarified.


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