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1998
DOI: 10.1002/(sici)1099-1565(199809/10)9:5<237::aid-pca411>3.3.co;2-l
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Taxane analysis by high performance liquid chromatography–Nuclear magnetic resonance spectroscopy of Taxus species

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Cited by 5 publications
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“…Today, the analysis of Taxus ingredients is performed mostly by high performance liquid chromatography (HPLC) using photodiode array (PDA) detection and mass spectrometry (MS, MS/MS, laser desorption/ionisation) detection . Besides nuclear magnetic resonance (NMR) and fluorescence detection was described. Immunological methods and thin layer chromatography have declined in significance …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Today, the analysis of Taxus ingredients is performed mostly by high performance liquid chromatography (HPLC) using photodiode array (PDA) detection and mass spectrometry (MS, MS/MS, laser desorption/ionisation) detection . Besides nuclear magnetic resonance (NMR) and fluorescence detection was described. Immunological methods and thin layer chromatography have declined in significance …”
Section: Introductionmentioning
confidence: 99%
“…Today, the analysis of Taxus ingredients is performed mostly by high performance liquid chromatography (HPLC) using photodiode array (PDA) detection [12][13][14][15][16][17][18][19][20][21][22][23][24][25] and mass spectrometry (MS, MS/MS, laser desorption/ionisation) detection. 10,21,[25][26][27][28][29][30][31] Besides nuclear magnetic resonance (NMR) 32,33 and fluorescence 34 detection was described.…”
Section: Introductionmentioning
confidence: 99%
“…In different combinations, these hyphenated techniques have already proven their value for the analysis of complex matrixes. [20][21][22][23][24] The on-line elucidation of relative or absolute configurations of chiral molecules right from crude extracts, however, without the use of chiral chromatographic phases, is still a demanding task, which has been accomplished only rarely. [25][26][27][28][29] In this paper, we present a screening procedure for this pharmacologically promising class of dimeric naphthylisoquinoline alkaloids.…”
mentioning
confidence: 99%
“…4). Other reported stopped-flow experiments deal with hop bitter acids [38], [65], starfish saponins [51], ecdysteroids of Silene otites (Caryophyllaceae) [39], [66], taxanes from Taxus species (Taxaceae) [67], metabolites from Anigozanthos species (Haemodoraceae) [68], [69], [70], lignans from Torreya jackii (Taxaceae) [71], extract of St. John's wort [72], Agromyces culture broth extract [73], a lignan glucoside from flax seed [74], flavonoids in Sorocea bomplandii (Moraceae) [75] and Trifolium pratense (Fabaceae) extract [76], protoberberine alkaloid fraction from Corydalis (Fumariaceae) cell cultures [77], [78], major metabolites of Aloe littoralis (Asphodelacaea) [79] (Fig. 5), flavonoid glycosides in transgenic tomatoes [80], sesame oil lignans [81], quinic acid derivatives from Fagara zanthoxyloides (Rutaceae) [82], betalain fraction from Hylocereus polyrhizus (Cactaceae) [83], phthalides from Ligusticum chuanxiong (Apiaceae) [84], and metabolites from several Chinese plants [85].…”
Section: Stopped-flow Measurementsmentioning
confidence: 99%