Indoles and auxins. VII. Active esters and anhydrides of 3-indoleacetic acid

1970 ◽  
Vol 48 (1) ◽  
pp. 177-179 ◽  
Author(s):  
Judith C. Hart ◽  
Eileen M. Matheson ◽  
O. Hutzinger

The synthesis of activated esters and anhydrides of 3-indoleacetic acid is described. Their usefulness for the preparation of amino acid derivatives is shown by reaction with glycine methyl ester.

1988 ◽  
Vol 41 (7) ◽  
pp. 1063 ◽  
Author(s):  
VA Burgess ◽  
CJ Easton

N-Benzoyl-2-bromoglycine methyl ester (1) reacted with the alkyl nitronates (2a-e) to give the corresponding β-nitro amino acid derivatives (4a-e). Elimination reactions of (4a-d) afforded the α,β-dehydro amino acid derivatives (5a-d). Treatment of the β- nitrovaline derivative (4b) with tributyltin hydride gave the valine derivative (8). Reduction of the β- nitroalanine derivative (4a) gave the β- aminoalanine derivative (9), characterized by hydrolysis to 2,3- diaminopropionic acid hydrochloride.


1965 ◽  
Vol 43 (3) ◽  
pp. 309-315 ◽  
Author(s):  
P. B. Hagen ◽  
W. Black

It has been possible to prepare the N-trifluoroacetyl methyl esters of the 19 amino acids commonly found in proteins and to separate them by gas chromatography on two types of column, Carbowax 1540 and Carbowax 20M. There is a constant relation between the amount of each amino acid and the size of the recorded peak. This indicates either that the conversion to the derivative is quantitative or that a constant proportion of each amino acid is converted to its N-trifluoroacetyl methyl ester.


1980 ◽  
Vol 1 (6) ◽  
pp. 523-532 ◽  
Author(s):  
S. Venitt ◽  
C. Crofton-Sleigh ◽  
S. L. Ooi ◽  
R. Bonnett

2004 ◽  
Vol 30 (2) ◽  
pp. 148-153 ◽  
Author(s):  
R. M. Kondratenko ◽  
L. A. Baltina ◽  
E. V. Vasil'eva ◽  
Kh. M. Nasyrov ◽  
R. M. Kireeva ◽  
...  

1973 ◽  
Vol 38 (14) ◽  
pp. 2518-2521 ◽  
Author(s):  
Joseph Kovacs ◽  
Richard E. Cover ◽  
Robert H. Johnson ◽  
Theodore J. Kalas ◽  
George L. Mayers ◽  
...  

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