2006
DOI: 10.1021/jf052267t
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Nonvolatiles of Commercial Lime and Grapefruit Oils Separated by High-Speed Countercurrent Chromatography

Abstract: The nonvolatile fractions of cold-pressed peel oils of Key and Persian lime as well as grapefruit were separated by high-speed countercurrent chromatography (HS-CCC). In addition to the isolation of the main coumarins, psoralens and polymethoxyflavones, a number of minor constituents were enriched and successfully characterized by GC-MS and HPLC-UV. 5,7,8-Trimethoxycoumarin and the cyclical acetals of oxypeucedanin hydrate with citral were determined as new nonvolatile trace constituents of lime oils and confi… Show more

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Cited by 37 publications
(28 citation statements)
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“…This is in agreement with the broad 1 H NMR methylene proton resonance at 1.23 ppm with a large integration value and the absence of other terminal methyl group resonances other than those of C-10′′ of the alkane substituent and of the geranyl C-3′ and C-7′ methyl groups. The assignment of an acetal group to C-1′′ of 1 is consistent with the observation of a 1 H NMR resonance at To further verify this structure, 1 was synthesized from 2 and decanal using reaction conditions for the synthesis of acetals, similar to that reported by Feger et al 11 The MS and the 1 H and 13 C NMR data of the synthesized product and the originally isolated 1 were identical. Marmin (2) was previously shown to possess an Rconfiguration, 18 and thus, 1 was identified as (R)-6′,7′-marmin decanal acetal.…”
supporting
confidence: 83%
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“…This is in agreement with the broad 1 H NMR methylene proton resonance at 1.23 ppm with a large integration value and the absence of other terminal methyl group resonances other than those of C-10′′ of the alkane substituent and of the geranyl C-3′ and C-7′ methyl groups. The assignment of an acetal group to C-1′′ of 1 is consistent with the observation of a 1 H NMR resonance at To further verify this structure, 1 was synthesized from 2 and decanal using reaction conditions for the synthesis of acetals, similar to that reported by Feger et al 11 The MS and the 1 H and 13 C NMR data of the synthesized product and the originally isolated 1 were identical. Marmin (2) was previously shown to possess an Rconfiguration, 18 and thus, 1 was identified as (R)-6′,7′-marmin decanal acetal.…”
supporting
confidence: 83%
“…The assignment of an acetal group to C-1′′ of 1 is consistent with the observation of a 1 H NMR resonance at δ 4.77 (H-1′′, t, J ) 4.72 Hz) and the 13 C NMR resonance at δ 101.2. 11 The 1 H NMR spectrum revealed three signals associated with protons (H-1′ δ 4.67; H-6′ δ 3.44; H-1′′ δ 4.77) covalently bonded to three alkoxy carbons (C-1′, C-6′, and C-1′′), whereas the 13 C NMR data provided evidence of four alkoxy carbons (C-1′ δ 65.1, C-6′ δ 83.6, C-7′ δ 78.7, and C-1′′ δ 101.2). These data supported a structure lacking…”
mentioning
confidence: 99%
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“…Further fractionation and separation of the CHCl 3 fraction by various chromatographic methods yielded ten coumarins, which were identified as osthol (1), meranzin (2), auraptenol (3), meranzin hydrate (4), 7-hydroxy-8-methoxy coumarin (5), imperatorin (6), xanthotoxol (7), xanthotoxin (8), bergapten (9) and isopimpinellin (10) (Fig. 1), by the direct comparison of their physicochemical and spectroscopic data with those previously reported [12][13][14][15][16]. Among the compounds isolated, compounds 2 and 5 are reported from this plant for the first time.…”
Section: Resultsmentioning
confidence: 66%
“…Além destes, outros sinais foram detectados entre δ 164,0-122,4, relativos aos carbonos sp 2 C-2/C-3 e C-6/C-7 da mistura isomérica. Através da comparação dos dados obtidos com aqueles descritos na literatura (Feger et al, 2006;Pihlasalo et al, 2007), foi possível identificar os dois monoterpenos na mistura.…”
Section: Resultsunclassified