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Table 2 1H and 13C NMR data of compounds 2 in chloroform-d

From: In vivo anti-malarial activity of the hydroalcoholic extract of rhizomes of Kniphofia foliosa and its constituents

Present data Reference data [35]
Position δC (ppm) δH (ppm) δC (ppm) δH (ppm)
1 161.69 12.6 (1H, s, −OH) 161.7 12.53 (1H, s, −OH)
1a 115.22 114.7
2 125.31 7.28 (1H, s) 124.6 7.32 (1H, q, J = 0.7 Hz)
3 152.44 151.6  
4 125.75 128.5  
4a 132.72 131.6  
5 120.11 7.55 (1H, dd, J = 1.5, 7 Hz) 119.3 7.56 (1H, dd, J = 1.5, 7 Hz)
5a 134.27 134.4  
6 137.12 7.57 (1H, dd, J = 7, 8 Hz) 137.4 7.75 (1H, dd, J = 7, 8 Hz)
7 123.85 7.21 (1H, dd, J = 1.5, 8 Hz) 123.3 7.30 (1H, dd, J = 1.5, 8 Hz)
8 159.51 11.9 (1H, s, -OH) 161.1 12.0 (1H, s, -OH)
8a 115.37 115.5
9 192.68 192.5
10 182.66 181.9
1’ 106.07 104.7
2’ 163.27 5.7 (1H, s (br), -OH) 163.3 8.95 (1H, s (br), -OH)
3’ 107.14 107.3
4’ 163.07 162.4
5’ 90.61 6.19 (1H, s) 91.2 6.24 (1H, s)
6’ 162.85 14.3 (1H, s, -OH) 161.9
ArCH3 21.02 2..21 (3H, s) 20.4 2.17 (3H, d, J = 0.7 Hz)
OCH3 55.56 3.91 (3H, s) 55.6 3.98 (3H, s)
COCH3 33.14 2.70 (3H, s) 32.6 2.62 (3H, s)
COCH3 202.3 202.3
  1. s, singlet, d, doublet, dd, doublet of doublets, q, quartet, m, multiplet, br, broad