2008
DOI: 10.3407/rpn.v2i1.15
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FLAVONOIDES DE Chromolaena subscandens (Hieron.) R.M. King & H. Rob.

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Cited by 3 publications
(1 citation statement)
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“…One-and two-dimensional nuclear magnetic resonance (NMR) spectra were recorded for the isolated compounds using deuterated dimethyl sulfoxide (DMSO-d 6 ). 1 H-and 13 C-NMR chemical shifts (see Supplementary Material) were in accordance with those reported for pinocembrin 1 [28][29][30], sakuranetin 2 [31][32][33][34], cirsimaritin 3 [26,[35][36][37], and naringenin 4 [27,28,[38][39][40][41]. An unambiguous assignment of the 13 C-NMR spectrum of these compounds was deduced from 1 H-1 H COSY, NOESY, HSQC, and HMBC spectra (see Supplementary Material).…”
Section: Column Chromatography Recrystallization Meohsupporting
confidence: 85%
“…One-and two-dimensional nuclear magnetic resonance (NMR) spectra were recorded for the isolated compounds using deuterated dimethyl sulfoxide (DMSO-d 6 ). 1 H-and 13 C-NMR chemical shifts (see Supplementary Material) were in accordance with those reported for pinocembrin 1 [28][29][30], sakuranetin 2 [31][32][33][34], cirsimaritin 3 [26,[35][36][37], and naringenin 4 [27,28,[38][39][40][41]. An unambiguous assignment of the 13 C-NMR spectrum of these compounds was deduced from 1 H-1 H COSY, NOESY, HSQC, and HMBC spectra (see Supplementary Material).…”
Section: Column Chromatography Recrystallization Meohsupporting
confidence: 85%