Literature DB >> 20236648

High-performance liquid chromatographic enantioseparation of aminonaphthol analogs on polysaccharide-based chiral stationary phases.

István Ilisz1, Zoltán Pataj, Róbert Berkecz, István Szatmári, Ferenc Fülöp, Antal Péter.   

Abstract

High-performance liquid chromatographic methods were developed for the separation of the enantiomers of five new aminonaphthol analogs possessing two chiral centers. The direct separations were performed on chiral stationary phases containing either amylose-tris-3,5-dimethylphenyl carbamate (Kromasil AmyCoat column) or cellulose-tris-3,5-dimethylphenyl carbamate (Kromasil CelluCoat column) as chiral selector. The experimental data are utilized to discuss the effects of the mobile phase composition, the nature of the alcoholic modifier and the specific structural features of the analytes on the retention and separation. The elution sequence was determined in all cases; no general regularities could be established. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20236648     DOI: 10.1016/j.chroma.2010.02.031

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  1 in total

1.  Separation of Betti Reaction Product Enantiomers: Absolute Configuration and Inhibition of Botulinum Neurotoxin A.

Authors:  John H Cardellina; Rebecca C Vieira; Vanessa Eccard; Janet Skerry; Vicki Montgomery; Yvette Campbell; Virginia Roxas-Duncan; William Leister; Christopher A Leclair; David J Maloney; Daniele Padula; Gennaro Pescitelli; Ilja Khavrutskii; Xin Hu; Anders Wallqvist; Leonard A Smith
Journal:  ACS Med Chem Lett       Date:  2011-03-10       Impact factor: 4.345

  1 in total

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