scholarly journals Glycine methyl or ethyl ester hydrochloride as the simplest examples of salty peptides and their derivatives.

1988 ◽  
Vol 52 (10) ◽  
pp. 2679-2681 ◽  
Author(s):  
Yoshihiro KAWASAKI ◽  
Takashi SEKI ◽  
Masahiro TAMURA ◽  
Eiichi KIKUCHI ◽  
Makoto TADA ◽  
...  
Keyword(s):  
Ethyl Ester ◽  
Ester Hydrochloride

The 4-(methylthio)phenyl ester for the synthesis of polypeptides of a known repeating sequence of amino acids. Synthesis of poly-(L-lysylglycyl)glycine 1-C14 ethyl ester hydrobromide

1970 ◽  
Vol 48 (16) ◽  
pp. 2509-2511 ◽  
Author(s):  
Brian J. Johnson ◽  
Donna S. Rea
Keyword(s):  
Amino Acids ◽  
Ethyl Ester ◽  
Title Compound ◽  
Ester Hydrochloride ◽  
Phenyl Ester ◽  
Protecting Group ◽  
High Dilution ◽  
Protective Groups ◽  
Protected Tetrapeptide

The synthesis of the tetrapeptide, N-t-butoxycarbonyl-ε-N-carbobenzoxy-L-lysylglycyl-ε-N-carbobenzoxy-L-lysylglycine 4-(methylthio)phenyl ester is described. The utility of this protective ester is shown by its easy conversion to the protected tetrapeptide 4-(methylsulfonyl)phenyl activated ester without decomposition. Removal of the N-butoxycarbonyl protecting group afforded the polymerizing unit, ε-N-carbobenzoxy-L-lysylglycyl-ε-N-carbobenzoxy-L-lysylglycine 4-(methylsulfonyl)phenyl ester. Polymerization of this material on the partially blocked monomer glycine-1-C14 ethyl ester hydrochloride, at a relatively high dilution, gave poly-(ε-N-carbobenzoxyl-L-lysylglycyl)glycine-1-C14 ethyl ester. The carbobenzoxy protective groups were removed to give the title compound.

Iron-Catalyzed Cyclopropanation with Glycine Ethyl Ester Hydrochloride in Water

2012 ◽  
Vol 14 (8) ◽  
pp. 2162-2163 ◽  
Author(s):  
Bill Morandi ◽  
Amund Dolva ◽  
E. M. Carreira
Keyword(s):  
Ethyl Ester ◽  
Ester Hydrochloride ◽  
Glycine Ethyl Ester

Vibrational and Structural Behavior of l-Cysteine Ethyl Ester Hydrochloride in the Solid State and in Aqueous Solution

2013 ◽  
Vol 117 (51) ◽  
pp. 14243-14252 ◽  
Author(s):  
M. E. Defonsi Lestard ◽  
S. B. Díaz ◽  
M. Puiatti ◽  
G. A. Echeverría ◽  
O. E. Piro ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Solid State ◽  
Ethyl Ester ◽  
Structural Behavior ◽  
Ester Hydrochloride

scholarly journals Ethyl (S)-2-Benzamido-5-[(4,6-dimethylpyrimidin-2-yl)amino]pentanoate

Molbank ◽  
10.3390/m1166 ◽  
2020 ◽  
Vol 2020 (4) ◽  
pp. M1166
Author(s):  
Mario Leyva-Acuña ◽  
Francisco Delgado-Vargas ◽  
Gabriela López-Angulo ◽  
Julio Montes-Avila
Keyword(s):  
Microwave Irradiation ◽  
Ethyl Ester ◽  
13C Nmr ◽  
Biological Activities ◽  
The Novel ◽  
Ester Hydrochloride ◽  
Pyrimidine Derivatives ◽  
Wide Range ◽  
Atr Spectroscopy ◽  
Moderate Yield

Pyrimidines are compounds with a wide range of biological activities, and the synthesis of pyrimidine derivatives—useful in chemical and medicinal applications—is important in medicinal chemistry. This work shows the synthesis under microwave irradiation of the novel compound ethyl (S)-2-benzamido-5-[(4,6-dimethylpyrimidin-2-yl)amino]pentanoate (3) from (S)-N-α-benzoyl-l-arginine ethyl ester hydrochloride (1) and acetylacetone (2). Compound 3 was easily purified, obtained in moderate yield (70%), and fully characterized by UV-Vis, FTIR-ATR spectroscopy, 1H-NMR, 13C-NMR, HRMS, and EI-MS.

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