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. 2016 Apr 26;21(5):549. doi: 10.3390/molecules21050549

Table 1.

1H, 13C and HMBC correlation data for tokinolide A (6) a.

Position δc, Type δH, (J in Hz) HMBC Position δc, Type δH, (J in Hz) HMBC
1 169.5, qC 1′ 175.4, qC
3 149.0, qC 3′ 151.4, qC
3a 151.4, qC 3a′ 48.2, qC
4 17.8, CH2 2.56 m, 2.40 m 5, 3a, 7a 4′ 29.7, CH2 1.94 m, 2.03 m 5′, 7, 3a′, 7a′
5 20.1, CH2 1.70 m, 2.12 m 4, 6, 7, 7a′ 5′ 21.0, CH2 2.10 m 7′, 3a′, 4′, 6′
6 40.2, CH 2.90 m 4, 5, 7, 1′,7a′ 6′ 131.1, CH 6.11 m 4′, 5′, 7a′
7 34.1, CH 3.23 d (9.4) 4′, 6, 3a, 7a, 3a′ 7′ 124.6, CH 6.00 d (9.8) 5′, 3a′, 7a′
7a 125.3, qC 7a′ 46.4, qC
8 112.1, CH 5.21 t (7.9) 3, 3a, 10 8′ 106.9, CH 4.66 dd (7.1, 8.3) 3′,3a′, 10′
9 27.9, CH2 2.36 m 3, 8, 10, 11 9′ 27.2, CH2 2.08 m, 1.90 m 3′, 8′, 10′, 11′
10 22.4, CH2 1.49 m 8, 9, 11 10′ 22.5, CH2 1.25 m 8′, 9′,11′
11 13.7, CH3 0.95 t (7.4) 9, 10 11′ 13.5, CH3 0.80, (7.4) 9′,10′

a Data obtained on a Varian 600 MHz instrument in CDCl3.