| Autor: |
Kula, Józef, Sikora, Magdalena, Hammad, Dina, Bonikowski, Radosław, Balawejder, Maciej, Nowicki, Janusz |
| Zdroj: |
Flavour & Fragrance Journal; Sep2005, Vol. 20 Issue 5, p487-491, 5p |
| Abstrakt: |
Starting from furfural and 5-methyfurfural, the furyl analogues of linalool, geraniol, citral, citronellol and citronellal, in which the isobutenyl moiety was replaced by a furyl substituent, have been synthesized. The olfactory properties of the new compounds prepared are of the corresponding parent terpene type; however, a positive influence of the methyl group in the furan ring on the odour was observed. The relative vapour pressures of furyl analogue alcohols were determined by SPME-GC and shown to be lower by a factor of 1.6-2.9 as compared to their corresponding parent terpene alcohols. Copyright © 2005 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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Plný text