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. 2017 Dec 29;16(1):5. doi: 10.3390/md16010005

Table 1.

1H NMR data for compounds 3 and 4 (600 MHz, CDCl3).

Position (3R,4S)-Epoxy-Pinnatifidenyne (3) (3S,4R)-Epoxy-Pinnatifidenyne (4)
δH (J in Hz) δH (J in Hz)
1 2.39, d (1.7) 2.38, d (1.7)
3 3.52, dd (1.7, 4.0) 3.44, dd (1.7, 4.0)
4 3.25, ddd (3.8, 4.0, 8.4) 3.12, ddd (4.0, 4.7, 7.6)
5 1.64, ddd (3.3, 8.4, 14.6)
2.35, ddd (3.8, 9.7, 14.6)
2.06, ddd (4.7, 7.0, 14.5)
2.14, ddd (7.6, 7.6, 14.5)
6 4.12, ddd (2.5, 3.3, 9.7) 4.03, ddd (2.6, 4.7, 7.6)
7 3.95, ddd (2.5, 5.0, 11.6) 4.08, ddd (2.6, 5.1,11.7)
8 2,55, ddd (5.0, 6.6, 11.8)
2.96, ddd (1.7, 11.6, 11.8)
2.56, ddd (5.8, 6.1, 12.5)
2.99, dddd (1.8, 11.6, 12.5)
9 5.72, dddd (1.7, 6.6, 10.1) 5.72, ddd (1.8, 6.1, 10.3)
10 5.93, br.dd (8.4, 10.1) 5.93, br.dd (8.5, 10.3)
11 2.44, ddd (1.3, 8.4, 14.0)
2.61, br.dd (3.7, 14.0)
2.37, ddd (1.0, 8.5, 13.9)
2.62, br.dd (3.8, 13.9)
12 3.65, ddd (1.3, 3.7, 10.0) 3.53, ddd (1.0, 3.8, 10.1)
13 3.97, ddd (3.0, 3.3, 10.0) 3.97, ddd (2.8, 3.5, 10.1)
14 1.79, ddq (3.3, 7.2, 14.5)
2.06, ddq (3.0, 7.2, 14.5)
1.80, ddq (2.8, 7.2, 14.5)
2.04, ddq (3.5, 7.2, 14.5)
15 1.08, t (7.2) 1.08, t (7.2)