4.6 Article

Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1357, 期 -, 页码 172-181

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2014.04.080

关键词

Cyclofructans; Atropisomers; Biaryls; Chiral HPLC; Preparative HPLC

资金

  1. National Institute of General Medical Sciences of the National Institutes of Health [R44GM103359]
  2. UT Southwestern Endowed Scholars in Biomedical Research Program
  3. Robert A. Welch Foundation [I-1764]
  4. ACS-PRF [51707-DNI1]
  5. American Cancer Society & Simmons Cancer Center Institutional Research Grant (New Investigator Award in Cancer Research) [ACS-IRG 02-196]

向作者/读者索取更多资源

Normal phase chiral HPLC methods are presented for the enantiomeric separation of 30 biaryl atropisomers including 18 new compounds recently produced via a novel synthetic approach. Three new cyclofructan based chiral stationary phases were evaluated. Separations were achieved for all but six analytes and the LARIHC (TM) CF6-P alone provided 15 baseline separations. Effects of polar modifiers and temperature effects also were studied. Apparent thermodynamic parameters were determined by van't Hoff plots. Preparative scale methods were developed and employed resulting in the first ever isolation of these novel atropisomers in their pure enantiomeric form. Insights into the mechanism of retention and chiral discrimination are presented. (C) 2014 Elsevier B.V. All rights reserved.

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