scholarly journals Anionic Hetero[3,3] Rearrangements.N-Acylhydroxylamine-O-carbamates to α-Amino Acids: A New Method for Introduction of Amino Groups at the α-Position of Carboxylic Acids

Synlett ◽  
1991 ◽  
Vol 1991 (09) ◽  
pp. 649-650 ◽  
Author(s):  
Yasuyuki Endo ◽  
Shoji Hizatate ◽  
Koichi Shudo
1976 ◽  
Vol 54 (20) ◽  
pp. 3310-3311 ◽  
Author(s):  
Francis C. M. Chen ◽  
N. Leo Benoiton

Methyl iodide and potassium bicarbonate in methanol is presented as a mild, efficient, and selective reagent for the quaternization of amino groups. It does not attack hydroxyl groups. Its use with amino acids, derivatives of lysine, and small peptides is described.


1968 ◽  
Vol 23 (5) ◽  
pp. 581-587 ◽  
Author(s):  
Klaus Dose ◽  
Sergio Risi

The formation of aliphatic α-amino acids by X-ray induced carboxylation of simple amines or amination of simple carboxylic acids is not favored over the formation of other amino acids. The new carboxylic and amino groups are more or less distributed statistically over the carbon atoms of the starting material. On radiationchemical formation of aliphatic hydrocarbons over C3, therefore, an increasing amount of unusual amino acids is produced. The results are influenced by various parameters such as temperature, pH, concentration, linear energy transfer and total dosis of radiation applied. Also peptides can be formed radiationchemically. However, the formation of greater molecules by radiationchemical processes under the conditions of a primitive earth seems to have only a low probability. The reaction mechanisms of radiationchemical carboxylation and amination are discussed.


Nature ◽  
1951 ◽  
Vol 168 (4266) ◽  
pp. 202-203 ◽  
Author(s):  
J. PORATH ◽  
P. FLODIN
Keyword(s):  

2008 ◽  
Vol 38 (23) ◽  
pp. 4107-4115 ◽  
Author(s):  
Qian Yang ◽  
Xiao-jian Wang ◽  
Zhi-yu Li ◽  
Li Sun ◽  
Qi-dong You

2017 ◽  
Vol 132 (7) ◽  
Author(s):  
Lorenzo Botta ◽  
Bruno Mattia Bizzarri ◽  
Davide Piccinino ◽  
Teresa Fornaro ◽  
John Robert Brucato ◽  
...  

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