Novel access to (3R)- and (3S)-3-hydroxy-L-aspartic acids, (4S)-4-hydroxy- L-glutamic acid, and related amino acids

1993 ◽  
Vol 71 (9) ◽  
pp. 1401-1406 ◽  
Author(s):  
Stephen Hanessian ◽  
Benoit Vanasse

Derivatives of L-aspartic and L-glutamic acids can be converted into α-hydroxy acids via oxygenation of the corresponding enolates.

1953 ◽  
Vol 51 (1) ◽  
pp. 140-144 ◽  
Author(s):  
J. Gordon

1. Glycine, alanine, and several isomers of alanine, DL-glutamic acid and DL-aspartic acid, when added to fresh guinea-pig serum and allowed to stand on the bench for half an hour, will protect the complement of this serum from destruction by heating at 55 and 56° C. for half an hour, but most of the complement activity is destroyed by heating at 57° C. and it is completely destroyed at 58° C. after half an hour.2. Derivatives of glycine do not have any protective effect.3. Various substances of high molecular weight, that might be described as ‘protective colloids’ do not have any protective effect.4. How these amino-acids when added to serum alter the heat-lability of the complement is not understood.


Molbank ◽  
10.3390/m1147 ◽  
2020 ◽  
Vol 2020 (3) ◽  
pp. M1147
Author(s):  
Giovanna Speranza ◽  
Marco Rabuffetti ◽  
Nikolina Vidović ◽  
Carlo F. Morelli

γ-Glutamyl derivatives of sulfur amino acids have been prepared in multigram scale starting from readily available starting materials. The synthesis comprises two one-pot operations, both consisting of two reactions. In the first operation, N-phtaloyl-l-glutamic acid anhydride is obtained from l-glutamic acid and phtalic anhydride. In the second one, N-phtaloyl-l-glutamic acid anhydride is used to acylate amino acids and the N-phtaloyl protecting group is removed. The described approach offers a viable entry to γ-glutamyl derivatives of sulfur-containing amino acids with flavor-enhancer and nutraceutical properties.


1977 ◽  
Vol 55 (6) ◽  
pp. 1387-1390 ◽  
Author(s):  
J. F. MacDonald ◽  
A. Nistri ◽  
A. L. Padjen

The effect of iontophoretically applied kainic acid diethylester (KDEE) on the firing rate of feline spinal interneurones was investigated and compared with the action of glutamic acid diethylester (GDEE) and aspartic acid diethylester (ADEE). All these esters reversibly reduced spontaneous neuronal firing and increased spike height, KDEE being the most active of this group. KDEE decreased responses to glutamate, acetylcholine, and peripheral field stimulation, showing that its depressant action is not due to a selective antagonism of an excitatory putative transmitter.


1979 ◽  
Vol 44 (8) ◽  
pp. 2556-2562 ◽  
Author(s):  
Michal Lebl ◽  
Anastasia Dimeli ◽  
Vera Bojanovska ◽  
Jiřina Slaninová ◽  
Tomislav Barth ◽  
...  

A number of amides of [4-glutamic acid]deamino-1-carba-oxytocin, as well as certain derivatives of amino acids, and a protected hydrazide of the above-mentioned peptide were prepared by a reaction with the amino-component, using dicyclohexylcarbodiimide and 1-hydroxybenzotriazole. The analogues were checked for uterotonic and galactogogic activity.


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