Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases

被引:37
|
作者
Woods, Ross M. [1 ]
Patel, Darshan C. [1 ]
Lim, Yeeun [1 ]
Breitbach, Zachary S. [1 ]
Gao, Hongyin [3 ]
Keene, Craig [3 ]
Li, Gongqiang [3 ]
Kuerti, Laszlo [3 ]
Armstrong, Daniel W. [1 ,2 ]
机构
[1] Univ Texas Arlington, Arlington, TX 76019 USA
[2] AZYP LLC, Arlington, TX 76019 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Biochem, Div Chem, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Cyclofructans; Atropisomers; Biaryls; Chiral HPLC; Preparative HPLC; HPLC; AUXILIARIES; IMPURITIES; CATALYSTS; SYNTHONS; RESOLUTION;
D O I
10.1016/j.chroma.2014.04.080
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:172 / 181
页数:10
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