2003
DOI: 10.1002/pca.730
|View full text |Cite
|
Sign up to set email alerts
|

Variation in the composition of the heartwood flavonoids of Prunus avium by on‐column capillary gas chromatography

Abstract: A fast and simple extraction procedure, coupled with on-column gas chromatography, has been developed in order to investigate the relative amounts of flavonoids in individual trees within several homogeneous populations of Prunus avium. Eight known flavonoid aglycones were isolated from the heartwood of P. avium and multivariate analysis was employed in order to characterise population groups.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
12
0
2

Year Published

2004
2004
2020
2020

Publication Types

Select...
6
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 19 publications
(16 citation statements)
references
References 25 publications
2
12
0
2
Order By: Relevance
“…More recently, two already cited studies devoted to woods employable in cooperage (Sanz et al, 2010;Sanz, Fern andez de Sim on, Esteruelas, et al, 2012) identified eriodictyol, naringenin, hesperetin and pinocembrin in seasoned and light toasted cherry wood, but not sakuranetin. The occurrence of this latter compound, whose UV and (MÀH) features are the same as its isomer isosakuranetin, was unambiguously ascertained by fortification experiments and confirms the findings of other researchers who indagued on P. avium heartwood (McNulty et al, 2009;Vinciguerra, Luna, Bistoni, & Zollo, 2003). Three further compounds (compounds #10, #11 and #16) displayed UV spectrum and MS fragmentation referable to flavanone aglycones (Fabre, Rustan, de Hoffmann, & QuetinLeclercq, 2001) and were tentatively assigned accordingly.…”
Section: Characterization Of Phenolics Extracted From Cherry Woodmentioning
confidence: 53%
See 1 more Smart Citation
“…More recently, two already cited studies devoted to woods employable in cooperage (Sanz et al, 2010;Sanz, Fern andez de Sim on, Esteruelas, et al, 2012) identified eriodictyol, naringenin, hesperetin and pinocembrin in seasoned and light toasted cherry wood, but not sakuranetin. The occurrence of this latter compound, whose UV and (MÀH) features are the same as its isomer isosakuranetin, was unambiguously ascertained by fortification experiments and confirms the findings of other researchers who indagued on P. avium heartwood (McNulty et al, 2009;Vinciguerra, Luna, Bistoni, & Zollo, 2003). Three further compounds (compounds #10, #11 and #16) displayed UV spectrum and MS fragmentation referable to flavanone aglycones (Fabre, Rustan, de Hoffmann, & QuetinLeclercq, 2001) and were tentatively assigned accordingly.…”
Section: Characterization Of Phenolics Extracted From Cherry Woodmentioning
confidence: 53%
“…Chrysin was the only flavone found in our extracts at quite an high concentration (around 70 mg/g). This compound has been described as one of the main flavonoid present in recently felled P. avium heartwood (Nagarajan & Parmar, 1977;Vinciguerra et al, 2003), at amounts of about 200 mg/g (Hasegawa, 1957). On the other hand, other researchers did not report chrysin among the flavonoids extracted from seasoned or toasted cherry wood (Sanz et al, 2010), suggesting the natural variability of the wood as raw material for cooperage.…”
Section: Characterization Of Phenolics Extracted From Cherry Woodmentioning
confidence: 94%
“…Alternative woods Nat (NS) Q. pyrenaica (I) [27] 2522 Q. pyrenaica (G) [23] 3940 ns ns ns ns 3940 ns ns ns ns ns ns ns 3940 Q. pyrenaica (H) [23] 20500 ns ns ns ns 20500 ns ns ns ns ns ns ns 20500 Robinia p. (A) [17] 2. 76…”
Section: Alternative Wood Species From Quercus Genusmentioning
confidence: 99%
“…TMS derivatives of flavonoids are stable, and give informative fragmentation ions under positive electron ionization (EI). The successful separation of TMS derivatives of flavonoids by GC followed by their mass spectrometric identification (GC-MS) has been reported by several researchers [19][20][21]. The ease of preparation and their excellent GC properties has led to an increased use of trimethylsilyl (TMS) derivatives for polar molecules for many compounds [22][23][24][25][26].…”
Section: Introductionmentioning
confidence: 99%