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DOI: 10.1039/A901388A (Paper) Reference Section for: Anal. Commun., 1999, 36, 149-151

Update on enantiomeric composition of (1R)-(+)- and (1S)-(–)-camphor in essential oils by enantioselective gas chromatography

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F. Tateo, M. Bononi, E. De Dominicis and V. Fumagalli

Abstract

The enantiomeric ratios of camphor have been determined in authentic essential oils, using heptakis(6-O-t-butylsilyl-2,3-di-O-ethyl)-β-cyclodextrin as the chiral stationary phase. An enantiomeric excess of (1S)-(–) within 72–75% is characteristic of coriander oil (Coriandrum sativum L.). Contrary, an enantiomeric excess of (1R)-(+) characterizes the essential oils of sage (>90% for Salvia sclarea L. and 50–70% for Salvia officinalis L.) and of basil (>94% for Ocimum basilicum L.).

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