STEREOISOMERIC FLAVOR COMPOUNDS - LXXX - ALKYL-BRANCHED ALKANALS - STEREODIFFERENTIATION, STRUCTURE ELUCIDATION AND STRUCTURE-FUNCTION RELATIONSHIP

Citation
D. Bartschat et A. Mosandl, STEREOISOMERIC FLAVOR COMPOUNDS - LXXX - ALKYL-BRANCHED ALKANALS - STEREODIFFERENTIATION, STRUCTURE ELUCIDATION AND STRUCTURE-FUNCTION RELATIONSHIP, ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG A-FOOD RESEARCH AND TECHNOLOGY, 206(3), 1998, pp. 165-168
Citations number
13
Categorie Soggetti
Food Science & Tenology
ISSN journal
14314630
Volume
206
Issue
3
Year of publication
1998
Pages
165 - 168
Database
ISI
SICI code
1431-4630(1998)206:3<165:SFC-L->2.0.ZU;2-S
Abstract
The direct enantioseparation of 2-methylbutanal, 2-methylpentanal, 2-e thylhexanal, 3-methylpentanal and 4-methylhexanal was achieved using e nantioselective gas chromatography and the chiral stationary phase hep takis-[2,3-di-O-acetyl-6-O-tert. butyldimethylsilyl]-beta-cyclodextrin (DIAC-TBDMS-beta-CD). Odour characteristics and threshold values of d etection for compounds were evaluated by enantioselective gas chromato graphy/olfactometry. Enantiopure reference compounds with defined abso lute configurations were synthesized starting from the corresponding a lcohols or acids which were commercially available or prepared in the laboratory.