1999
DOI: 10.1016/s0021-9673(99)01036-5
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Characterisation of hydrolysable tannins from leaves of Betula pubescens by high-performance liquid chromatography–mass spectrometry

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Cited by 152 publications
(167 citation statements)
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“…Individual phenolics in the fraction of polar compounds (0.1 ml) were studied by using the high-performance liquid chromatography (HPLC) diode-array detection system as in Salminen et al (1999), except that the solvents used were (1) 0.05 M of H 3 PO 4 , and (2) acetonitrile. A selected set of samples was also analyzed with HPLC electrospray ionization mass spectrometry as in Salminen et al (1999), except that the data system used was Analyst Software 1.1.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Individual phenolics in the fraction of polar compounds (0.1 ml) were studied by using the high-performance liquid chromatography (HPLC) diode-array detection system as in Salminen et al (1999), except that the solvents used were (1) 0.05 M of H 3 PO 4 , and (2) acetonitrile. A selected set of samples was also analyzed with HPLC electrospray ionization mass spectrometry as in Salminen et al (1999), except that the data system used was Analyst Software 1.1.…”
Section: Methodsmentioning
confidence: 99%
“…A selected set of samples was also analyzed with HPLC electrospray ionization mass spectrometry as in Salminen et al (1999), except that the data system used was Analyst Software 1.1. Phenolics were identified on the basis of their UV, mass spectra, and retention times.…”
Section: Methodsmentioning
confidence: 99%
“…The HPLC system (Merck-Hitachi, Tokyo, Japan) consisted of a pump L-7100, a diode array detector L-7455, a programmable autosampler L-7250, and an interface D-7000. Column and chromatographic conditions were as described earlier (Salminen et al, 1999), except that 0.1 M H 3 PO 4 was replaced with 0.05 M H 3 PO 4 . Lipophilic flavonoid aglycones were identified on the basis of their UV and mass spectra and retention times as reported in the literature (Valkama et al, 2003), and quantified (absolute amounts) as acacetins (flavonols and flavones) or naringenins (flavanones).…”
Section: Methodsmentioning
confidence: 99%
“…According to the literature, the main characteristic in the mass spectra of these compounds was the deprotonated molecula [M-H] - (m/z 483, 635, 787, 939, 785, 937) and the loss of one or more galloyl groups (152 mu) and/or gallic acid (170 mu) (Salminen et al, 1999;Zywicki et al, 2002) As far as we know, there was no information on the phenolic composition of C. sativa and R. micrantha flowers, but a few previous studies have been published dealing with the phenolic composition of F. ulmaria flowers from Russia Krasnov et al, 2009;Shilova et al, 2006), Poland (Fecka, 2009) and Austria (Pemp et al, 2007). Some differences were found in the F. ulmaria sample (flowers from Portugal) studied herein, including the presence of different compounds such as isorhamnetin glucoside derivatives and caffeic acid derivatives.…”
Section: Hydrolyzable Tanninsmentioning
confidence: 99%