2006
DOI: 10.1016/j.phytochem.2006.01.014
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An unusual glucoside from Cleistanthus gracilis

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Cited by 10 publications
(10 citation statements)
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“…Thereafter the extracts were concentrated in a rotatory evaporator at 40 °C to dryness. The crude extracts were fractionated based on the partition method of Charaux-Paris using solvents with increasing polarities (Pinho et al, 2006;Silva et al, 2012). Thus, to 1 g of crude extract 50 mL of n-hexane was added and centrifuged at 5500 g, 20 min, 4 °C.…”
Section: Preparation Of Heather Extracts and Fractionationmentioning
confidence: 99%
“…Thereafter the extracts were concentrated in a rotatory evaporator at 40 °C to dryness. The crude extracts were fractionated based on the partition method of Charaux-Paris using solvents with increasing polarities (Pinho et al, 2006;Silva et al, 2012). Thus, to 1 g of crude extract 50 mL of n-hexane was added and centrifuged at 5500 g, 20 min, 4 °C.…”
Section: Preparation Of Heather Extracts and Fractionationmentioning
confidence: 99%
“…The crude methanolic extracts were fractionated using the Charaux-Paris method, which consists in a sequential liquid-liquid partition with n-hexane (Fraction 1), diethyl ether (Fraction 2) and water (Fraction 3) ( Figure 3) [41,42]. This process allows obtaining fractions with different and increasing polarities.…”
Section: Extraction and Fractionationmentioning
confidence: 99%
“…4). Lupeol (21) and 3-oxofriedelin (22) were isolated from the stem and roots of C. gracilis (Pinho et al 2006).…”
Section: Triterpenesmentioning
confidence: 99%
“…Recently, gracicleistanthoside (28) has been isolated from the stem and roots of C. gracilis Hook. f., collected from Thailand (Pinho et al 2006). Figure 6 shows the structure of ellagic acid (27) Acetylation of gracicleistanthoside (28) gave rise to the acetate 29 whose structure was established by 1 H, 13 CNMR, COSY, NOESY, HSQC, HMBC and HRMS.…”
Section: Miscellaneousmentioning
confidence: 99%
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