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. 2022 Aug 4;70(32):9834–9844. doi: 10.1021/acs.jafc.2c02502

Table 2. 1H and 13C NMR Data of Truncatenoneab.

no. δCc δH (J in Hz) HMBC
1 14.8 q 1.89 (3H) d (6.8) H-2
2 138.3 d 6.79 (1H) q (6.8) H3C-1, H3C-9
3 138.2 s   H3C-1, H3C-9
4 207.2 s   H-2, H-5, H-6, H3C-9, H3C-10
5 43.1 d 3.30 (1H) quint (7.2) H2C-7, H3C-10
6 75.6 d 3.63 (1H) m H-5, H2C-7, H3C-8, H3C-10
7 27.9 t 1.50 (1H) m H3C-8
    1.43 (1H) m  
8 10.1 q 0.97 (3H) t (7.4) H-6, H2C-7
9 10.8 q 1.78 (3H) s H-2
10 16.0 q 1.15 (3H) d (7.2) H-5
a

2D 1H, 1H (COSY), and 13C, 1H (HSQC) NMR experiments confirmed the correlations of all of the protons and the corresponding carbons.

b

Coupling constants (J) are given in parentheses.

c

Multiplicities were assigned to the DEPT spectrum.