Chiral GC analysis of (1 R )(+)‐pulegone with high enantiomeric purity in essential oils of some lamiaceae aromatic plants | Zendy

Ravid Uzi | Zendy; Putievsky Eli | Zendy; Katzir Irena | Zendy

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Chiral GC analysis of (1 R )(+)‐pulegone with high enantiomeric purity in essential oils of some lamiaceae aromatic plants

Author(s) -

Ravid Uzi,

Putievsky Eli,

Katzir Irena

Publication year - 1994

Publication title -

flavour and fragrance journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.393

H-Index - 70

eISSN - 1099-1026

pISSN - 0882-5734

DOI - 10.1002/ffj.2730090410

Subject(s) - pulegone , lamiaceae , chemistry , enantiomer , essential oil , monoterpene , enantiomeric excess , stereochemistry , chromatography , organic chemistry , botany , enantioselective synthesis , biology , catalysis

(1 R )(+)‐Pulegone with high enantiomeric purity (95–100%) was detected in the essential oils from fresh leaves of Mentha piperita L., M. longifolia (L.) Huds., M. pulegium L., M. sylvestris L., Calamintha incána (Sm.) Heldr. and Micromeria fruticosa . L. High enantiomeric purities were found in samples of commercial (+)‐ and (—)‐pulegone. Direct enantiomeric separation was performed using a Cyclodex B chiral capillary column.

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