Traditional Herbal Medicine Research Methods 2010
DOI: 10.1002/9780470921340.ch4
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Identification and Structure Elucidation of Compounds from Herbal Medicines

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Cited by 3 publications
(2 citation statements)
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“…IR can take place in the near-, mid- or far-infrared regions, or use a Fourier Transform method to simultaneously beam many frequencies, repeated in bursts of different combinations over a short time and then calculate the absorbance at each wavelength. The near range, from 780–2,526 nm is the most commonly used in quality control due to having higher energy and penetration capacity and producing less heat ( Zeng et al, 2011 ) while the mid-infrared spectrum (2.5–25 µm) is superior for identifying structure and functional groups ( Liang et al, 2011 ).…”
Section: Resultsmentioning
confidence: 99%
“…IR can take place in the near-, mid- or far-infrared regions, or use a Fourier Transform method to simultaneously beam many frequencies, repeated in bursts of different combinations over a short time and then calculate the absorbance at each wavelength. The near range, from 780–2,526 nm is the most commonly used in quality control due to having higher energy and penetration capacity and producing less heat ( Zeng et al, 2011 ) while the mid-infrared spectrum (2.5–25 µm) is superior for identifying structure and functional groups ( Liang et al, 2011 ).…”
Section: Resultsmentioning
confidence: 99%
“…Compound ICW-V-a had a molecular ion at m/z 597 [M-H] À . It also showed an ion at m/z 477 [M-120-H] À that indicates a characteristic fragment ion of C-glycosyl flavonoids (Liang, Jin, Feng, & Ke, 2011). It has 1 H NMR and 13 C NMR spectral data as the followings: 1 H NMR (CD 3 OD, 500 MHz): phloretin (aglycone) moiety d7.03 (2H, d, J = 8.4 Hz, H2 and H6), 6.67 (2H, d, J = 8.4 Hz, H3 and H5), 3.34 (2H, m, Ha), 2.85 (2H, m, Hb); glucose moiety d4.93 (2H, d, J = 9.8 Hz, H1 00 , H1 00 0 ), 3.84 (2H, dd, J = 12.2 Hz and 2.1 Hz, H6a 00 , H6a 00 0 ), 3.80 (2H, dd, J = 12.2 Hz and 4.2 Hz, H6b 00 , H6b 000 ), 3.61 (2H, dd, J = 9 Hz and 9.5 Hz, H2 00 , H2 00 0 ), 3.54 (2H, dd, J = 9 Hz and 9 Hz, H3 00 , H3 00 0 ), 3.50 (2H, dd, J = 8.8 Hz and 8.8 Hz, H4 00 , H4 00 0 ), 3.42 (2H, m, H5 00 , H5 00 0 ).…”
Section: Analysis and Identification Of Phenolic Compounds In Extractmentioning
confidence: 99%