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. 2023 Feb 7;86(2):380–389. doi: 10.1021/acs.jnatprod.2c01007

Table 3. NMR Spectroscopic Data (500 MHz, CDCl3) of 9-Methoxycrotokilwaepoxide A (3).

position δC, type δH (J in Hz) HMBCa
1 211.3, C    
2 36.9,CH 2.57, ddq (8.4, 8.4, 7.1) C-1, C-3, C-19
3 34.2, CH2 1.69 dd (13.9, 8.4) C-2, C-4, C-5, C-19
    2.90 dd (13.9, 8.4)  
4 61.4, C    
5 57.8, CH 3.09 s C-3, C-4, C-6, C-20
6 57.3, C    
7 38.0, CH 3.02 d (12.8) C-6, C-8, C-9, C-13, C-14, C-15
8 158.7, C    
9 109.8, C    
OMe-9 52.0, CH3 3.55 s C-9
10 30.5, CH2 1.75 ddd (15.0, 13.9, 4.0) C-9, C-11, C-12
    2.67 ddd (15.0, 3.9, 3.6) C-8, C-9, C-11, C-12
11 32.9, CH2 1.49 ddd (13.8, 4.0, 3.6) C-9, C-10, C-13, C-18
    2.15 ddd (13.9, 13.8, 3.9) C-9, C-10, C-12, C-13
12 58.4, C    
13 35.7, CH 3.07 d (12.8) C-7, C-8, C-11, C-12, C-14, C-18
14 64.3, C    
15 129.9, C    
16 170.8, C    
17 10.0, CH3 1.95 s C-6, C-7, C-8, C-9, C-10, C-15, C-16
18 57.9, CH2 2.78 s C-11, C-12, C-13
19 13.1, CH3 1.11 d (7.1) C-1, C-2, C-3
20 20.5, CH3 1.15 s C-6, C-7
a

HMBC correlations, optimized for 6 Hz, are from the stated proton(s) to the indicated carbon.