Infinite enantiomeric resolution of basic compounds using highly sulfated cyclodextrin as chiral selector in capillary electrophoresis

2003 ◽  
Vol 24 (15) ◽  
pp. 2633-2641 ◽  
Author(s):  
Serge Rudaz ◽  
Enrica Calleri ◽  
Laurent Geiser ◽  
Samir Cherkaoui ◽  
Josiane Prat ◽  
...  
2014 ◽  
Vol 35 (19) ◽  
pp. 2759-2764 ◽  
Author(s):  
Margarita V. Lebedeva ◽  
Aleksandra F. Prokhorova ◽  
Elena N. Shapovalova ◽  
Oleg A. Shpigun

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

2000 ◽  
Vol 14 (4) ◽  
pp. 203-213 ◽  
Author(s):  
Ricardo Batista Borges ◽  
Antonio Laverde Jr. ◽  
André Luiz Meleiro Porto ◽  
Anita Jocelyne Marsaioli

Racemic and chiral ethyl-phenylsulfoxide (solute) andβ-cyclodextrin (chiral selector) were used to compare two NMR methodologies to predict RP-HPLC enantiomeric resolution efficiency. One of them based on the classical approach involving apparent binding constants and complexation‒induced chemical shifts at saturation and the other based on13C NMR signal splittings (solute and chiral selector in stoichiometric ratio) and HR-DOSY of the same solution. We have concluded that the latter methodology is rather efficient and though more elaborate from the NMR point of view, the results are promising and constitute an alternative method to investigate chiral recognition and other supramolecular phenomena.


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