Preparative separation of amino acid enantiomers as N-TFA, O-isopropyl derivatives by continuous countercurrent gas-liquid chromatography

Preparative separation of derivatives of amino acid enantiomers was carried out by a countercurrent gas–liquid chromatography (CCGLC) with chiral liquid phases, N‐stearoyl‐L‐valine tert‐butylamide and/or N‐stearoyl‐L‐leucine tert‐butylamide. In order to make effective use of these phases and also to...

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Veröffentlicht in:Chirality (New York, N.Y.) N.Y.), 1993, Vol.5 (4), p.246-249
Hauptverfasser: Sato, Katsuya, Watabe, Katsunori, Ihara, Toshihide, Hobo, Toshiyuki
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Sprache:eng
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Zusammenfassung:Preparative separation of derivatives of amino acid enantiomers was carried out by a countercurrent gas–liquid chromatography (CCGLC) with chiral liquid phases, N‐stearoyl‐L‐valine tert‐butylamide and/or N‐stearoyl‐L‐leucine tert‐butylamide. In order to make effective use of these phases and also to lower the viscosity, Apiezon C was added as diluent. Through a repeated operation of a temperature gradient, purities more than 99% of leucine and α‐amino butyric acid derivatives were proved to be obtained. © 1993 Wiley‐Liss, Inc.
ISSN:0899-0042
1520-636X
DOI:10.1002/chir.530050411