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The 3,5\u2010dimethylphenyl carbamoylated cellulose columns were effective in both normal and rev ersed\u2010phase modes. The effects of the mobile phase composition, the pH, the buffer concentration, and the structures of the substituents on the 2\u2010naphthol on the enantioseparations were studied. The absolute configuration and elution sequence were determined for 1\u2010(1\u2010amino\u20102\u2010methylpropyl)\u20102\u2010naphthol: the elution sequence was <jats:italic>S<\/jats:italic> &lt; <jats:italic>R<\/jats:italic>. Chirality, 2007. \u00a9 2007 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/chir.20392","type":"journal-article","created":{"date-parts":[[2007,3,22]],"date-time":"2007-03-22T19:41:09Z","timestamp":1174592469000},"page":"374-379","source":"Crossref","is-referenced-by-count":20,"title":["High\u2010performance liquid chromatographic enantioseparation of 1\u2010(aminoalkyl)\u20102\u2010naphthol analogs on polysaccharide\u2010based chiral stationary 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