High??performance liquid chromatographic enantioseparation of Betti base analogs on a newly developed isopropyl carbamate??cyclofructan6??based chiral stationary …
…, I Ilisz, Z Pataj, I Szatmári, F Fülöp, DW Armstrong…
Index: Aranyi, Anita; Ilisz, Istvan; Pataj, Zoltan; Szatmari, Istvan; Fueloep, Ferenc; Armstrong, Daniel W.; Peter, Antal Chirality, 2011 , vol. 23, # 7 p. 549 - 556
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Citation Number: 12
Abstract
Abstract The direct separation of the enantiomers of 1-(α-aminoarylmethyl)-2-naphthol, 1-(α- aminoalkyl)-2-naphthol, 2-(α-aminoarylmethyl)-1-naphthol analogs, and 2-(1-amino-2- methylpropyl)-1-naphthol) was performed on a newly developed chiral stationary phase containing isopropyl carbamate-cyclofructan6 as chiral selector, with n-heptane/alcohol/ trifluoroacetic acid as mobile phase. The effects of the mobile-phase composition, the ...
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