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. Author manuscript; available in PMC: 2021 Oct 1.
Published in final edited form as: Bioorg Chem. 2020 Jul 23;103:104127. doi: 10.1016/j.bioorg.2020.104127

Table 2.

1H and 13C NMR Data for Eucalyprobusones C (8) and D (9).

Eucalyprobusone C (8)a Eucalyprobusone D (9)b
No. δC δH (J in Hz) δC δH (J in Hz)
1 165.8 163.6
2 104.6 104.0
3 162.5 162.0
4 93.6 6.10 s 92.8 6.07 s
5 164.4 162.8
6 110.3 106.0
7 211.3 211.1
8 39.9 3.82 sept. (6.7) 39.3 3.79 sept. (6.8)
9 19.6 1.13 d (6.7) 19.2 1.17 d (6.8)
10 19.7 1.12 d (6.7) 19.2 1.17 d (6.8)
1′ 165.8 169.9
2′ 104.6 105.6
3′ 162.5 165.3
4′ 93.6 6.10 s 104.8
5′ 164.4 168.4
6′ 110.3 103.5
7′ 211.6 15.1 3.74 2H s
8′ 27.8 a 1.79 m, b 1.35 m 193.2 10.15 s
9′ 46.7 3.69 sext. (6.7) 207.2
10′ 16.8 1.11 d (6.7) 52.2 3.00 2H d (6.7)
11′ 16.9 1.11 d (6.7) 25.2 2.44 brsept. (6.7)
12′ 22.7 0.99 d (6.7)
13′ 22.7 0.99 d (6.7)
1″ 28.2 5.01 t (8.1)
2″ 40.8 2.08 2H m
3″ 27.4 1.44 brsept. (6.5)
4″ 22.8 0.88 d (6.5)
5″ 22.8 0.88 d (6.5)
OH-1 9.50 s 16.76 s
OH-1′ 9.50 s 17.23 s
OH-3′ 10.31 s
OH-5 8.93 s
OH-5′ 14.48 s
OMe-3 56.2 3.90 s 55.8 3.86 s
OMe-3′ 56.2 3.89 s
a

Data were recorded at 600 MHz in acetone-d6.

b

Data were recorded at 500 MHz in CDCl3.