Skip to main content
. 2019 Dec 11;19:361. doi: 10.1186/s12906-019-2776-1

Table 1.

1H NMR (CDCl3, 600 MHz) and 13C NMR (CDCl3, 151 MHz) spectral data of compound 1

Position δH (ppm) δC(ppm) HMBC
1 1.25 (21H, m) 14.3 C-2
2 4.15 (2H, q, J = 7.1 Hz) 60.1 C-1, C-3
3 174.3
4 2.31 (2H, t, J = 7.7 Hz)) 35.0 C-3, C-5, C-6
5 1.60 (2H, m) 29.1 C-4
6 1.32 (21H, m) 24.9 C-5
7 2.79 (2H, m) 35.0 C-8
8 5.41 (1H, m) 130.0 C-6
9 5.41 (1H, m) 130.0
10 2.02 (2H, m) 31.9 C-11, C-9
11 1.35 (21H, m) 29.7 C-13
12 1.25 (21H, m) 2.8 C-11
13 0.85 (4H, t, J = 7.1 Hz)) 14.3 C-11, C-12