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. 2011 Aug 4;16(8):6582–6590. doi: 10.3390/molecules16086582

Table 1.

1H-NMR and 13C-NMR spectral data of (+)-kunstlerone (1) in CDCl3 (δ in ppm, J in Hz).

Position 1H 13C
C-1′ - 132.12
C-2′ 6.80, br s 107.25
C-3′ - 147.97
C-4′ - 146.39
C-5′ 6.76, d, (8.1) 108.32
C-6′ 6.71, br d, (8.1) 119.69
C-1 - 46.01
C-2 4.32, s 79.11
C-3 - 159.47
C-4 - 138.46
C-5 - 193.10
C-6 2.90, d, (8.5) 50.16
C-7 3.21, dd,
(7.8, 8.5)
44.58
C-8 2.83, m 49.63
C-9 3.72, dd,
(9.5, 3.9)
3.90, d, (9.5)
70.84
C-10 2.38, m 41.76
C-11 5.66, m 136.51
C-12 5.13, d, (Jcis = 11.0),
5.11, d, (Jtrans = 16.5)
119.41
OCH2O 5.91, s 101.08
3-OCH3 4.08, s 58.46
4-OCH3 3.69, s 60.57