Chiral amino alcohols derived from natural amino acids as chiral solvating agents for carboxylic acids

2008 ◽  
Vol 19 (10) ◽  
pp. 1193-1199 ◽  
Author(s):  
Wenge Wang ◽  
Xiumin Shen ◽  
Fengnian Ma ◽  
Zijing Li ◽  
Cong Zhang
2019 ◽  
Vol 55 (44) ◽  
pp. 6297-6300 ◽  
Author(s):  
Ciarán C. Lynch ◽  
Zeus A. De los Santos ◽  
Christian Wolf

Optical chirality sensing of unprotected amino acids, hydroxy acids, amino alcohols, amines and carboxylic acids based on a practical mix-and-measure protocol with readily available copper, iron, palladium, manganese, cerium or rhodium salts is demonstrated.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 444
Author(s):  
Zuzanna Wrzeszcz ◽  
Renata Siedlecka

Interesting properties of N-oxides and pyridine oxazoline compounds have become the starting point to synthesize compounds connecting both groups. A multi-step synthesis of a series of chiral oxazoline substituted pyridine N-oxides, alkyl derived of pyridine N-oxides, bipyridine N-oxides, and isoquinoline N-oxides, based on amino alcohols derived from natural amino acids or other previously prepared, is presented herein. Various synthetic pathways have been designed and tested according to the properties and limitations imposed by the target products. The encountered problems related to the stability of the products were discussed. The resulting compounds (eighteen structures) were tested as catalysts in th e allylation of benzaldehyde (obtaining up to 79% ee) as well as in nitroaldol reaction (obtaining up to 48% ee).


1961 ◽  
Vol 39 (6) ◽  
pp. 1309-1320 ◽  
Author(s):  
Patrice Tailleur ◽  
Louis Berlinguet

Using classical methods of synthesis nine small peptides containing amino-1 cycloalkyl carboxylic acids have been synthesized. The cyclic acids have been placed either at the N-terminal or at the C-terminal positions or in between two natural amino acids, glycine and DL-phenylalanine.The cyclization of two dipeptides into a substituted diketopiperazine, and the subsequent hydrolysis of this compound have been studied.


2015 ◽  
Vol 51 (9) ◽  
pp. 1232-1244 ◽  
Author(s):  
S. A. Koshkin ◽  
A. R. Garifzyanov ◽  
N. V. Davletshina ◽  
O. N. Kataeva ◽  
D. R. Islamov ◽  
...  

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