1984
DOI: 10.1016/s0021-9673(00)96248-4
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On-line high-performance liquid chromatography

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Cited by 79 publications
(22 citation statements)
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“…For the remaining constituents, LC/UV with post-column addition of shift reagents was utilised in order to determine substitution pattern, including the presence of oxygenated groups and the position of the sugar, or other component, linked to the aglycone [11]. Although the derivatisation technique was originally developed for use in conjunction with conventional UV analysis of flavonoids employing methanol as solvent [12], it has also been shown to be appropriate for acidic solvents, such as the formic acid:acetonitrile:methanol mixture utilised in the LC analysis of Maytenus extracts. All phenolic groups, except for those in the peri position to a keto function, are affected by the presence of strong base (sodium hydroxide), while Al 3+ forms a complex with ortho-dihydroxy groups or keto groups having a hydroxyl in the peri position.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…For the remaining constituents, LC/UV with post-column addition of shift reagents was utilised in order to determine substitution pattern, including the presence of oxygenated groups and the position of the sugar, or other component, linked to the aglycone [11]. Although the derivatisation technique was originally developed for use in conjunction with conventional UV analysis of flavonoids employing methanol as solvent [12], it has also been shown to be appropriate for acidic solvents, such as the formic acid:acetonitrile:methanol mixture utilised in the LC analysis of Maytenus extracts. All phenolic groups, except for those in the peri position to a keto function, are affected by the presence of strong base (sodium hydroxide), while Al 3+ forms a complex with ortho-dihydroxy groups or keto groups having a hydroxyl in the peri position.…”
Section: Resultsmentioning
confidence: 99%
“…Eleven glycosylated flavonoids were determined in M. ilicifolia, the two major components being quercetin-di-rhamno-hexoside (3) and kaempferol-di-rhamno-pentoside (8), neither of which were detected in M. aquifolium. M. ilicifolia also showed the presence of a diglycosylated quercetin derivative (6) and rutin (13), together with four diglycosylated kaempferol derivatives (11,12,16 and 18), two monoglycosylated quercetin derivatives (14 and 15) and quercitrin (19). The presence in M. ilicifolia of rutin, quercitrin and the monoglycosylated flavonoids 14 and 15 has not been previously reported [7].…”
mentioning
confidence: 99%
“…Useful information was also obtained with the post-column addition of UV shift reagents according to a protocol already tested for flavonoids and xanthones. 19,20 The shifted and original UV spectra were overlaid and compared for each peak, and the shifts were interpreted according to data reported in the literature. 21 These analyses provided important complementary information on the structural features and oxygenation pattern for the on-line identification.…”
Section: Lc/uv/ms Analysismentioning
confidence: 99%
“…All three peaks on the mass spectrum showed the same m/z value for the parent ion peak (Figure 2) confirming the same molecular weight of the analyte (indicator dye) when performed in the negative ion mode [M-H + = 433]. [9][10][11][12][13][14][15][16][17][18] A comparison of the HPLC retention times and mass spectral data for the indicator is presented in Table 1.…”
Section: Spectral Analysismentioning
confidence: 77%