Reactivity of α-amino acids in the N-acylation with benzoic acid esters in aqueous dioxane

2010 ◽  
Vol 80 (5) ◽  
pp. 964-967 ◽  
Author(s):  
N. R. Ishkulova ◽  
L. E. Oparina ◽  
L. B. Kochetova ◽  
T. P. Kustova ◽  
N. V. Kalinina ◽  
...  
2006 ◽  
Vol 76 (1) ◽  
pp. 45-47
Author(s):  
L. V. Kuritsyn ◽  
A. I. Sadovnikov ◽  
L. N. Khripkova ◽  
N. V. Kalinina ◽  
Yu. S. Shcherbakova

1980 ◽  
Vol 35 (6) ◽  
pp. 727-730
Author(s):  
Oemer Saygin ◽  
Peter Decker

Abstract Nonenzymatic catalysis by bivalent ions of Be, Mg, Ca, Zn, Mn, Ni and Co and bioorganic phosphates of the formation of hydroxamic acids from acetate or amino acids has been studied systematically. Increased yields of hydroxamate were observed at particular combinations of reactants. The most prominent increase (ca. 15-fold) was found with acetate and Ni++, and with a combination of ATP and Be++. Among others especially ribose-5-phosphate and glucose-5-phosphate enhanced yields in the presence of most metal ions. Since no release of inorganic phosphate was observed, this effect cannot be interpreted as an evidence for intermediate transhosphorylation reactions; it may also result from simple catalytic effects of metal sugar complexes.


1973 ◽  
Vol 4 (40) ◽  
pp. no-no
Author(s):  
D. A. HOOGWATER ◽  
D. N. REINHOUDT ◽  
T. S. LIE ◽  
J. J. GUNNEWEG ◽  
H. C. BEYERMAN

2020 ◽  
Vol 56 (17) ◽  
pp. 2642-2645 ◽  
Author(s):  
Zhi-Fang Yang ◽  
Chang Xu ◽  
Xing Zheng ◽  
Xingang Zhang

A nickel-catalyzed tandem reaction of N-vinylamides with arylboronic acids and bromodifluoroacetate has been developed. The reaction efficiently furnishes a series of protected α,α-difluoro-γ-amino acid esters.


1958 ◽  
Vol 36 (10) ◽  
pp. 1436-1440 ◽  
Author(s):  
Paul E. Gagnon ◽  
Jean L. Boivin ◽  
Joseph Zauhar

Ethyl-, propyl-, and benzyl-guanidine nitrates were prepared from amine nitrates and calcium cyanamide or dicyandiamide. Carboxyalkylguanidines were made by condensing the corresponding amino acids with guanidine carbonate in aqueous medium. All the guanidine nitrates, except the benzyl derivative, were converted into the corresponding nitroguanidines by treatment with concentrated sulphuric acid. Esters and metal salts of 1-(α-carboxyalkyl)-2-nitroguanidines were also prepared.


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