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. 2021 Mar 4;84(3):724–737. doi: 10.1021/acs.jnatprod.0c01217

Table 5. 1H, 13C, and 13C DEPT NMR Data of Compounds 6 and 9a.

  6
9
position δH δC, type δH δC, type
1 4.93 br d (2.5) 71.2, CH 4.17 br d (4.5) 80.2, CH
2a 3.59 br d (16.0) 34.6, CH2 3.01 dd (17.0, 3.6) 35.5, CH2
2b 3.10 dd (16.0, 7.5)   2.40 br d (17.0)  
3   170.9, C   171.0, C
4   84.7, C   82.0, C
5 2.41b 44.8, CH 2.25 br t (8.7) 55.8, CH
6a 2.13b 26.3, CH2 1.94 m 25.3, CH2
6b 1.95 ddd (15.0, 7.5, 2.5)      
7 4.56 br d (2.5) 74.6, CH 4.65 br s 74.7, CH
8   41.8, C   45.0, C
9 2.87 d (2.0) 39.9, CH 2.67 d (5.0) 46.9, CH
10   45.4, C   46.0, C
11 5.25 m 68.5, CH 5.38 m 69.4, CH
12a 2.45b 38.2, CH2 2.55 dd (14.4, 10.0) 39.0, CH2
12b 1.62b   1.70b  
13   41.8, C   40.0, C
14   68.5, C   69.1, C
15 3.70 s 54.1, CH 3.61 s 56.8, CH
16   169.4, C   168.2, C
17 5.51 s 77.0, CH 5.52 br s 78.8, CH
18 1.41 s 18.3, CH3 1.36 s 19.4, CH3
19a 1.53 s 17.2, CH3 5.12 d (14.0) 67.9, CH2
19b     4.53 d (14.0)  
20   165.0, C   164.0, C
21 6.14 br s 97.4, CH 6.12 br s 97.8, CH
22 6.32 br s 124.3, CH 6.35 br s 124.6, CH
23   168.4, C   169.3, C
28 1.40 s 34.2, CH3 1.39 s 29.6, CH3
29 1.60 s 23.6, CH3 1.13 s 20.5, CH3
30 1.30 s 21.1, CH3   21.4, CH3
COCH3-1 2.15 s 21.6, CH3    
COCH3-1   169.4, C    
COCH3-7 2.15 s 20.2, CH3 2.20 s 21.6, CH3
COCH3-7   169.4, C   169.5, C
COCH3-11 2.15 s 21.1, CH3 2.15 s 21.4, CH3
COCH3-11   169.4, C   170.5, C
a

Spectra were recorded in CDCl3 at 600 MHz (1H) and 150 MHz (13C). J values are in parentheses and reported in Hz; chemical shifts are given in ppm; assignments were confirmed by 1D-TOCSY, COSY, HSQC, and HMBC experiments.

b

Overlapped signal.