Stereoselective analysis of herbicides by capillary electrophoresis using sulfobutyl ether β-cyclodextrin as chiral selector

1997 ◽  
Vol 18 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Claudia Desiderio ◽  
Chiara M. Polcaro ◽  
Salvatore Fanali
Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2611
Author(s):  
Daniel Kawano ◽  
Bruna Costa ◽  
Katherine Romero-Orejón ◽  
Hugo Loureiro ◽  
Dosil de Jesus ◽  
...  

1-Pyrrolines are important intermediates of active natural products, such as the 2,5-dialkyl-1-pyrroline derivatives found in fire ant venoms. Here, 5-hexyl-2-methyl-3,4-dihydro-2H-pyrrole was synthesized by the enzymatic transamination/cyclization of 2,5-undecadione, and enantiodifferenciation was successfully achieved by capillary electrophoresis with sulfobutyl ether-β-cyclodextrin as the chiral selector. The rationale of the enantiomeric discrimination was based on the results of a docking simulation that revealed the higher affinity of (S)-5-hexyl-2-methyl-3,4-dihydro-2H-pyrrole for the sulfobutyl ether-β-cyclodextrin.


Chirality ◽  
2007 ◽  
Vol 19 (5) ◽  
pp. 380-385 ◽  
Author(s):  
Yan Zhao ◽  
Xing-Bin Yang ◽  
Qiao-Feng Wang ◽  
Peng-Juan Nan ◽  
Ying Jin ◽  
...  

Chirality ◽  
1994 ◽  
Vol 6 (6) ◽  
pp. 496-509 ◽  
Author(s):  
Daniel W. Armstrong ◽  
Kimber L. Rundlett ◽  
Jing-Ran Chen

2004 ◽  
Vol 507 (2) ◽  
pp. 171-178 ◽  
Author(s):  
Juan José Martı́nez-Pla ◽  
Yolanda Martı́n-Biosca ◽  
Salvador Sagrado ◽  
Rosa Marı́a Villanueva-Camañas ◽  
Marı́a José Medina-Hernández

Sign in / Sign up

Export Citation Format

Share Document