Characterization of naphthalene dicarboxylic acids. 3. Separation on Dowex 1-× 8 anion-exchange resin

Fuel ◽  
1975 ◽  
Vol 54 (3) ◽  
pp. 185-186
Author(s):  
Clive Davies
1955 ◽  
Vol 6 (4) ◽  
pp. 391-408 ◽  
Author(s):  
F. Amer ◽  
D. R. Bouldin ◽  
C. A. Black ◽  
F. R. Duke

1957 ◽  
Vol 35 (1) ◽  
pp. 1249-1258
Author(s):  
A. M. Marko

Optimum conditions for the separation of the acidic amino acids glutamic, aspartic, and cysteic on an anion exchange resin, Dowex-1 × 8, have been studied. The sample to be analyzed is adjusted to pH 7 and placed on a column of Dowex-1 × 8 previously equilibrated with 0.1 M acetate buffer at pH 4. Glutamic and aspartic acids are separated by elution with 0.1 M acetate buffer at pH 4.0–4.6. Cysteic acid is eluted with 0.2 M acetate buffer at pH 5.5–5.9. With this method quantitative separation of synthetic mixtures of the acidic amino acids has been achieved. This method has also been used to determine the dicarboxylic amino acids in acid hydrolyzates of various proteins, of normal protein-free plasma, and of normal urine.


2010 ◽  
Vol 52 (5) ◽  
pp. 565-569 ◽  
Author(s):  
M. Sadeghi ◽  
M. Mirzaii ◽  
Z. Gholamzadeh ◽  
P. Sarabadani ◽  
A. Sattari

2014 ◽  
Vol 69 (5) ◽  
pp. 605-614 ◽  
Author(s):  
Nazar Pidlypnyi ◽  
Sandra Kaul ◽  
Sebastian Wolf ◽  
Martin H. H. Drafz ◽  
Andreas Schmidt

3-Methylindole reacts with pyridines in the presence of NBS to give indol-2-yl-pyridinium salts which were converted into their ylides by an anion exchange resin in its hydroxide form. Indol-3- amine was subjected to a nucleophilic ring transformation with pyrylium salts which resulted in the formation of indol-3-yl-pyridinium salts, the 2,4,6-trimethylpyridinium derivative of which proved to be unstable. The 2,4,6-triphenylpyridinium derivate was deprotonated to the corresponding ylide. The isomeric indol-2-yl and indol-3-yl derivatives are cycloimmonium ylides which are members of the compound class of heterocyclic mesomeric betaines (MB). By contrast, the ylide of indol- 2-yl-pyrrolidinium is a cycloammonium ylide. It was prepared by reaction of 3-methylindole with pyrrolidine in the presence of NBS, followed by deprotonation.


1957 ◽  
Vol 35 (12) ◽  
pp. 1249-1258 ◽  
Author(s):  
A. M. Marko

Optimum conditions for the separation of the acidic amino acids glutamic, aspartic, and cysteic on an anion exchange resin, Dowex-1 × 8, have been studied. The sample to be analyzed is adjusted to pH 7 and placed on a column of Dowex-1 × 8 previously equilibrated with 0.1 M acetate buffer at pH 4. Glutamic and aspartic acids are separated by elution with 0.1 M acetate buffer at pH 4.0–4.6. Cysteic acid is eluted with 0.2 M acetate buffer at pH 5.5–5.9. With this method quantitative separation of synthetic mixtures of the acidic amino acids has been achieved. This method has also been used to determine the dicarboxylic amino acids in acid hydrolyzates of various proteins, of normal protein-free plasma, and of normal urine.


1995 ◽  
Vol 23 (1) ◽  
pp. 101-108
Author(s):  
M. Fini ◽  
G. Giavaresi ◽  
M Spighi ◽  
R. Giardino ◽  
M. L. Florio

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