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. Author manuscript; available in PMC: 2016 Mar 27.
Published in final edited form as: J Nat Prod. 2015 Jan 28;78(3):552–556. doi: 10.1021/np501028u

Table 3.

13C NMR Spectroscopic Data of Compounds 1–3 [δc, ppm]a

carbon 1 2 3
C-1 54.4 61.6 61.8
C-3 37.4 44.1b 44.1b
C-4 29.1 22.5 23.1
C-4a 125.7 124.9 129.5
C-5 105.1 105.0 105.8
C-6 146.8 146.6 152.3
C-7 133.6 133.9 137.1
C-8 141.1 141.9 148.2
C-8a 123.2 122.6 121.6
C-α 38.4 39.6 39.3
C-9 134.5 135.5 135.7
C-10 115.4 115.0 115.0
C-11 149.9 149.4 149.4
C-12 147.4 147.2 147.3
C-13 111.4 111.6 111.7
C-14 122.2 123.0 123.1.
C-1′ 65.2 65.2 65.2
C-3′ 51.2 51.1 51.4
C-4′ 24.2 24.1 24.2
C-4a′ 122.3 122.2 122.0
C-5′ 132.9 133.1 132.5
C-6′ 137.7 138.1 138.8
C-7′ 151.1 151.1 151.2
C-8′ 105.7 106.1 106.3
C-8a′ 146.5 147.0 147.4
C-α′ 40.8 41.0 41.2
C-9′ 134.5 134.1 134.1
C-10′ 131.1 131.0 131.1
C-11′ 120.3 120.0 119.9
C-12′ 153.4 153.9 153.9
C-13′ 120.3 120.0 120.0
C-14′ 133.0 132.9 132.7
N-Me - 42.6 42.8
6-OMe 56.3 56.3 56.0
7-OMe - - 56.5
12-OMe 56.2 56.3 56.2
N′-Me 44.1 44.1b 44.1b
6′-OMe 60.6 60.8 60.6
7′-OMe 56.2 56.2 56.5
a

Recorded in CDCl3 at 100 MHz and 300 K

b

Overlapped signals