The Flavonoids 1975
DOI: 10.1007/978-1-4899-2909-9_1
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Isolation Techniques for Flavonoids

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Cited by 51 publications
(47 citation statements)
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“…It was obtained as a white, crystalline substance. Compound structure was confirmed by chromatographic and spectroscopic methods (13). …”
Section: Isolation and Identification Of Compoundmentioning
confidence: 96%
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“…It was obtained as a white, crystalline substance. Compound structure was confirmed by chromatographic and spectroscopic methods (13). …”
Section: Isolation and Identification Of Compoundmentioning
confidence: 96%
“…Quercetin-3,4'-diglucoside, kaempferol-3,4'-diglucoside and isorhamnetin-3,4'-diglucoside were isolated from the herb Echinocystis lobata and its structure elucidation was based on UV, 1 H NMR, 13 C NMR and MS data (12). The standards were dissolved in methanol (1 mg mL -1 ).…”
Section: Chemicalsmentioning
confidence: 99%
“…3'-and 4'-hydroxyl groups. 14 The glycoside on hydrolysis with dilute HCl afforded an aglycone which exhibited a 18 nm hypsochromic shift in band I in the UV spectrum in presence of AlCl 3 /HCl with respect to AlCl 3 indicating an orthodihydroxyl system in either ring A or B. The presence of orthodihydroxylgroup in ring B was ruled out by another spectrum in NaOAc/H 3 BO 3 as stated above.…”
Section: Resultsmentioning
confidence: 89%
“…Compound 1 afforded UV data, which suggested free hydroxyls at C-5, C-7, and C-4 [8][9][10]. The assignment of the 1 H and 13 C NMR data supported by NOESY and HMBC correlations confirmed the aglycone as isorhamnetin (3'-O-methylquercetin) substituted at C-3.…”
Section: Resultsmentioning
confidence: 99%