2007
DOI: 10.1590/s0103-50532007000100011
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On-line LC/UV/MS analysis of flavonols in the three apple varieties most widely cultivated in Brazil

Abstract: Este trabalho apresenta a primeira investigação sobre a estrutura química dos flavonóis presentes em cascas das três variedades de maçãs mais cultivadas no Brasil: Gala, Golden e Fuji. As análises foram feitas por CL/UV/EM (cromatografia líquida de alta eficiência com detector UV com arranjo de diodos acoplada à espectrometria de massas), usando adição pós-coluna de reagentes de deslocamento de UV e também espectrometria de massas de múltiplos estágios (EM n ) com ionização "electrospray" no modo negativo. A i… Show more

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Cited by 33 publications
(19 citation statements)
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“…The most common flavonoids in food are flavone/flavonol O-glycosides and flavone C-glycosides (Rayyan et al, 2010). In some fruits, such as apples, flavonols are usually O-glycosylated at the C-3 position (Tiberti et al, 2007). In some fruits, such as apples, flavonols are usually O-glycosylated at the C-3 position (Tiberti et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The most common flavonoids in food are flavone/flavonol O-glycosides and flavone C-glycosides (Rayyan et al, 2010). In some fruits, such as apples, flavonols are usually O-glycosylated at the C-3 position (Tiberti et al, 2007). In some fruits, such as apples, flavonols are usually O-glycosylated at the C-3 position (Tiberti et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…The flavonoid glycosides occur mainly as 3-or 7-O-glycosides, but the C-5, -6, -8 and -4 0 positions are sometimes glycosylated as well. In some fruits, such as apples, flavonols are usually O-glycosylated at the C-3 position (Tiberti et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…The individual MS 2 base peak at m/z 135 of peak 3 was resulted from the loss of a CO 2 moiety from corresponding deprotonated ion (Zhang et al, ). Peak 8 showed the [M–H] – at m/z 301, which was attributed to the aglycone quercetin, while the MS 2 spectrum showed the formation of m/z 179 (X – ) ion due to the fragmentation of rings A and B (Tiberti, Yariwake, Ndjoko, & Hostettmann, ). Peaks 4, 5, and 6 ([M−H] − at m/z 515) could be assigned as 3,4‐ O ‐, 3,5‐ O ‐, and 4,5‐ O ‐dicaffeoylquinic acids, respectively, based on their elution order, fragmentation pattern, and relative abundances (Clifford et al, ).…”
Section: Resultsmentioning
confidence: 99%
“…The individual MS 2 base peak at m/z 135 of peak 3 was resulted from the loss of a CO 2 moiety from corresponding deprotonated ion (Zhang et al, 2015). Peak 8 showed the [M-H]at m/z 301, which was attributed to the aglycone quercetin, while the MS 2 spectrum showed the formation of m/z 179 (X -) ion due to the fragmentation of rings A and B (Tiberti, Yariwake, Ndjoko, & Hostettmann, 2007). Peaks with published data (Mattonai, Parri, Querci, Degano, & Ribechini, 2016).…”
Section: Identification and Quantification Of Phenolic Compounds Inmentioning
confidence: 87%
“…The structure of the isolated substance was identified as glycosylated flavonoid quercetrin (quercetin-3-O-a-L-rhamnoside, 1), a yellow amorphous powder, by uni-and bidimensional NMR spectroscopic data analysis (UV, ESI-MS, and 1 H and 13 C NMR) and by comparing with data from literature (Correia et al, 2008;Tiberti et al, 2007).…”
Section: Chemical Constituents Of S Chilensismentioning
confidence: 99%