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Table 1 1H and 13C-NMR and Chemical Shifts of compound (ppm, CDCl3, 500 and 100 MHz, respectively).

From: Anti-spasmodic action of crude methanolic extract and a new compound isolated from the aerial parts of Myrsine africana

C. No Multiplicity (DEPT) 13C-NMR 1H (J= Hz)
1 CH2 38.5 1.71(m # of H), 1.93(m, #of H)
2 CH2 32.3 1.59 m, 1.83 m
3 CH 72.4 3.44 br m (w 1/2 = 12.5)
4 CH2 43.0 2.21 dd, 2.23 dd
5 C 140.8 ------
6 CH 121.8 5.53 br d (5.0)
7 CH2 32.8 1.81 m, 1.97 m
8 CH 31.8 1.61 m
9 CH 51.7 0.95 m
10 C 36.5 ------
11 CH2 22.0 1.01 m, 1.42 m
12 CH2 40.9 1.69 m, 1.40 m
13 C 41.3 ------
14 CH 57.8 1.09 m
15 CH2 32.7 1.49 m, 1.63 m
16 CH 82.2 4.39 q like (7.5)
17 CH 63.7 1.75 m
18 CH3 19.8 1.06 s
19 CH3 14.9 0.80 s
20 CH 29.9 1.60 m
21 CH3 17.5 0.72 d (J 21,20 = 6.5)
22 CH2 33.2 1.2 dd (overlapped), 1.50 dd (overlapped)
23 C 110.5 ------
24 CH 42.9 1.84 dd (5.5, 4.5)
25 CH2 32.4 1.65 m, 1.81 m
26 CH2 67.9 3.35 m, 3.42 m
27 CH3 16.8 0.95 d (J 27,24 = 6.5)