Improved gas chromatographic stereodifferentiation of chiral main constituents from different essential oils using a mixture of chiral stationary phases | Zendy

Bayer Mathias | Zendy; Mosandl Armin | Zendy

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Improved gas chromatographic stereodifferentiation of chiral main constituents from different essential oils using a mixture of chiral stationary phases

Author(s) -

Bayer Mathias,

Mosandl Armin

Publication year - 2004

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.1429

Subject(s) - chemistry , linalool , linalyl acetate , nerolidol , limonene , chromatography , essential oil , terpineol , enantioselective synthesis , lavender , monoterpene , organic chemistry , geraniol , gas chromatography , enantiomer , stationary phase , catalysis

The simultaneous enantioselective gas chromatographic differentiation of the chiral main compounds of lavender, neroli, petitgrain and bitter orange oil [limonene, linalool, linalool oxides (furanoid), linalyl acetate, ( E )‐nerolidol, α ‐pinene, β ‐pinene, terpinen‐4‐ol and α ‐terpineol] is described, using a dened mixture of heptakis(2,3‐di‐ O ‐methyl‐6‐ O ‐ tert ‐butyldimethylsilyl)‐ β ‐cyclodextrin and heptakis(2,3‐di‐ O ‐acetyl‐6‐ O ‐ tert ‐butyldimethylsilyl)‐ β ‐cyclodextrin as the chiral stationary phase. Copyright © 2004 John Wiley & Sons, Ltd.

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