1983
DOI: 10.1080/00021369.1983.10865931
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Pyridine Derivatives in Peppermint Oil

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Cited by 3 publications
(9 citation statements)
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“…From the in‐depth analysis of these 4 peppermint oils, 177 components were identified as being present (Figure 1, Table 2), including many trace components. This reported composition is in agreement with the previous literature (Sakurai and others 1983; Ishihara and others 1992; Näf and Velluz 1998; Gaudin, 2000; Frérot and Bagnoud 2002, 2004). Certain trends were observed between the 1st‐ and 2nd‐cut oils and also the fresh leaves and dried hay oil analyses.…”
Section: Resultssupporting
confidence: 93%
“…From the in‐depth analysis of these 4 peppermint oils, 177 components were identified as being present (Figure 1, Table 2), including many trace components. This reported composition is in agreement with the previous literature (Sakurai and others 1983; Ishihara and others 1992; Näf and Velluz 1998; Gaudin, 2000; Frérot and Bagnoud 2002, 2004). Certain trends were observed between the 1st‐ and 2nd‐cut oils and also the fresh leaves and dried hay oil analyses.…”
Section: Resultssupporting
confidence: 93%
“…Pyridine and five other derivatives, 2,6-dimethylpyridine, 5-ethyl-2-methylpyridine, 3-phenylpyridine, 3-phenyl-4-propylpyridine, and 5-phenyl-2-propylpyridine, had been already identified as the basic components of Mitcham peppermint oil (Takahashi et al, 1980;Sakurai et al, 1983). It is also reported that phenylpyridine derivatives have very strong characteristic odors and are representative of an odor profile of the basic fraction of peppermint oil.…”
Section: Methodsmentioning
confidence: 98%
“…4-Isopropyl-2-methylpyridine was prepared according to the method of Comins and Abdullah (1982) in 52% yield. The spectral data were as follows: RI = 1059; IR (film) 3080, 3030, 2975,1603,1560,920,830 cm"1; NMR (CDC13) 1.20 (d, «7 = 7 Hz, 6 H, two CH3), 2.47 (s, 3 H, CH3), 2.79 (dq, «7=7 and 7 Hz, 1H, CH), 6.84 (d, «7 = 5 Hz, , H), 6.87 (s, , H), 8.25 (d, «7 = 5 Hz, 1H, Ar H); EI-MS m/z (relative intensity) 135 (M+, 64), 120 (100), 106 (4), 93 (6), 77 (13), 65 (5), 42 (6), 41 (6). 3-Phenyl-4-propylpyridine was prepared from 3-phenylpyridine and butyric acid according to the modified method of Minisci et al (1971), and it showed the same physicochemical properties as those reported by Sakurai et al (1983).…”
Section: Methodsmentioning
confidence: 99%
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