Modified GC-phases for the enantiomeric separation of optically active compounds: Crosslinking experiments with polymeric chiral compounds

1985 ◽  
Vol 8 (8) ◽  
pp. 391-394 ◽  
Author(s):  
G. Schomburg ◽  
I. Benecke ◽  
G. Severin
1949 ◽  
Vol 71 (2) ◽  
pp. 460-462 ◽  
Author(s):  
Albert. Pohland ◽  
Frederick J. Marshall ◽  
Thomas P. Carney

Molecules ◽  
2018 ◽  
Vol 23 (8) ◽  
pp. 2003 ◽  
Author(s):  
Takatsugu Murata ◽  
Tatsuya Kawanishi ◽  
Akihiro Sekiguchi ◽  
Ryo Ishikawa ◽  
Keisuke Ono ◽  
...  

Various optically active 2-hydroxyamide derivatives are produced based on the kinetic resolution of racemic 2-hydroxyamides with a diphenylacetyl component and (R)-benzotetramisole ((R)-BTM), a chiral acyl-transfer catalyst, via asymmetric esterification and acylation. It was revealed that a tertiary amide can be used with this novel protocol to achieve high selectivity (22 examples; s-value reaching over 250). The resulting chiral compounds could be transformed into other useful structures while maintaining their chirality.


RSC Advances ◽  
2018 ◽  
Vol 8 (37) ◽  
pp. 20483-20487 ◽  
Author(s):  
Tomoyuki Ikai ◽  
Naoya Nagata ◽  
Seiya Awata ◽  
Yuya Wada ◽  
Katsuhiro Maeda ◽  
...  

We have succeeded in developing triptycene-based chiral stationary phases with a distorted cyclic structure, which can resolve a series of axially chiral compounds.


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