Determination of the Absolute Configuration of Amines and α-Amino Acids by1H NMR of (R)-O-Aryllactic Acid Amides†

1996 ◽  
Vol 61 (21) ◽  
pp. 7285-7290 ◽  
Author(s):  
Rafael Chinchilla ◽  
Larry R. Falvello ◽  
Carmen Nájera
2021 ◽  
Author(s):  
Eryn Nelson ◽  
Jeffrey S. S. K. Formen ◽  
Christian Wolf

The widespread occurrence and significance of chiral compounds does not only require new methods for their enantioselective synthesis but also efficient tools that allow rapid determination of the absolute configuration,...


Tetrahedron ◽  
2002 ◽  
Vol 58 (34) ◽  
pp. 6873-6879 ◽  
Author(s):  
Kiyonaga Fujii ◽  
Yukie Yahashi ◽  
Tomoyo Nakano ◽  
Susumu Imanishi ◽  
Susana F Baldia ◽  
...  

2006 ◽  
Vol 59 (6) ◽  
pp. 407 ◽  
Author(s):  
Luigi Aurelio ◽  
Robert T. C. Brownlee ◽  
Jason Dang ◽  
Andrew B. Hughes ◽  
Gideon M. Polya

We report the full structural determination of the depsipeptide petriellin A. The absolute configuration of the amino acid residues, N-methyl isoleucine and N-methyl threonine, have been determined by a combination of HPLC and TLC comparison of synthetic Marfey’s derivatives and Marfey’s derivatives of the natural product hydrolysate. The configuration of the chiral centres in these two N-methylated residues was found to be the same as those of the common unmethylated l-amino acids.


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