1981
DOI: 10.1016/s0021-9673(00)82664-3
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Chromatographic investigation of jasmin absolutes

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1989
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Cited by 16 publications
(37 citation statements)
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“…To simplify the experiment, we used only indole in jasind, but at a slightly higher level (6%) than in natural jasmine oil to compensate for the lack of para-cresol. We note that the components in the model jasmine we created are present in natural jasmine (Verzele et al, 1981;Toda et al, 1983;Kaiser, 1988) with the exception of hexylcinnamic aldehyde, which has been found to be a useful building block of jasmine odor, and that the components in the model are sufficient to capture many aspects of natural jasmine.) All stimuli were diluted 1:5 in dipropylene glycol in such a way that the eight components would be present at the same level in jasmine and jasind regardless of the presence of indole.…”
Section: Methodsmentioning
confidence: 99%
“…To simplify the experiment, we used only indole in jasind, but at a slightly higher level (6%) than in natural jasmine oil to compensate for the lack of para-cresol. We note that the components in the model jasmine we created are present in natural jasmine (Verzele et al, 1981;Toda et al, 1983;Kaiser, 1988) with the exception of hexylcinnamic aldehyde, which has been found to be a useful building block of jasmine odor, and that the components in the model are sufficient to capture many aspects of natural jasmine.) All stimuli were diluted 1:5 in dipropylene glycol in such a way that the eight components would be present at the same level in jasmine and jasind regardless of the presence of indole.…”
Section: Methodsmentioning
confidence: 99%
“…1), [17][18][19][20][21] (+)-(S)-geranyllinalool (6) (Fig. 3), [26][27][28][29][30][31][32][33][34][35][36] and the cembranoids (−)-(R)-nephthenol (7) 37-44 and 11,12-epoxysarcophytol A (8) ( Signals for four methyl groups, seven methylene groups, and six methine groups were identified by 1 H NMR, 13 C NMR, and DEPT measurements. Complete proton to carbon assignment was achieved by HSQC and HMBC measurements (Table S2 †).…”
Section: Sinularia Gravismentioning
confidence: 99%
“…35 Thus, it plays a decisive role in the fragrance of jasmine. 26,30,34 Whilst the laevorotatory (R)-enantiomer has been described frequently, the dextrorotatory (S)-enantiomer is rare. It has been found in jasmine oil 26 and in the freshwater aquatic plant Potamogeton pectinatus.…”
Section: Sinularia Gravismentioning
confidence: 99%
“…To simplify the experiment, we used only indole in jasind, but at a slightly higher level (6%) than in usual jasmine oil to compensate for the lack of para-cresol. We note that the components in the model jasmine we created are present in natural jasmine (Demole, 1982;Kaiser, 1988;Toda et al, 1983;Verzele et al, 1981) with the exception of hexylcinnamic aldehyde which has been found to be a useful building block of jasmine odor (Demole, 1982), and that the components in the model are sufficient to capture many aspects of natural jasmine.) All stimuli were diluted 1:5 in dipropylene glycol in such a way that the 8 components would be present at the same level in jas and jasind regardless of the presence of indole.…”
Section: Stimulimentioning
confidence: 99%