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Separation of Racemate from Excess Enantiomer of Chiral Nonracemic Compounds via Density Gradient Ultracentrifugation

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2008

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Journal of the American Chemical Society : JACS. 2008, 130(8), pp. 2426-2427. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja067905i

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In this study, it is shown that preparative density gradient ultracentrifugation can be applied to separate racemate crystals from excess enantiomer crystals. This was demonstrated for alanine crystals separated in a 50 wt % Nycodenz gradient. The recovery rates of the pure enantiomers from the mixtures were good (70−90%), and the separation method showed accuracy in the third digit of the density. As such density differences between racemate and enantiomers can be found for a wide range of crystalline chiral compounds, the presented separation method should be applicable to a large variety of substances on a preparative scale.

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ISO 690MASTAI, Yitzhak, Antje VÖLKEL, Helmut CÖLFEN, 2008. Separation of Racemate from Excess Enantiomer of Chiral Nonracemic Compounds via Density Gradient Ultracentrifugation. In: Journal of the American Chemical Society : JACS. 2008, 130(8), pp. 2426-2427. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja067905i
BibTex
@article{Mastai2008-02Separ-40113,
  year={2008},
  doi={10.1021/ja067905i},
  title={Separation of Racemate from Excess Enantiomer of Chiral Nonracemic Compounds via Density Gradient Ultracentrifugation},
  number={8},
  volume={130},
  issn={0002-7863},
  journal={Journal of the American Chemical Society : JACS},
  pages={2426--2427},
  author={Mastai, Yitzhak and Völkel, Antje and Cölfen, Helmut}
}
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    <dcterms:abstract xml:lang="eng">In this study, it is shown that preparative density gradient ultracentrifugation can be applied to separate racemate crystals from excess enantiomer crystals. This was demonstrated for alanine crystals separated in a 50 wt % Nycodenz gradient. The recovery rates of the pure enantiomers from the mixtures were good (70−90%), and the separation method showed accuracy in the third digit of the density. As such density differences between racemate and enantiomers can be found for a wide range of crystalline chiral compounds, the presented separation method should be applicable to a large variety of substances on a preparative scale.</dcterms:abstract>
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