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. Author manuscript; available in PMC: 2017 Feb 1.
Published in final edited form as: Phytochemistry. 2015 Nov 26;122:113–118. doi: 10.1016/j.phytochem.2015.11.011

Table 1.

1H and 13C NMR spectroscopic data for kalkipyrone B (2)a, b.

position αC, type αH, (J in Hz) COSY HMBC NOESYc
1 162.1, qC
2 99.3, qC
3 181.0, qC
4 118.0, qC
5 157.2, qC
6 29.9, CH2 3.29 d (7.3) 7, 17, 18 5, 7, 8 17
7 116.8, CH 5.21 ovlp 6, 17, 18 6, 9, 17 9
8 138.8, qC
9 39.2, CH2 2.00 t (7.7) 10 7, 8, 10, 11, 17
10 25.9, CH2 1.52 m 9, 11 8, 9
11 38.9, CH2 1.93 t (7.7) 10 9, 10, 12, 13, 16
12 137.4, qC
13 129.0, CH 5.20 ovlp 14, 16 11, 16 11, 15
14 64.7, CH 4.58 m 13, 15 12, 13 15, 16
15 23.5, CH3 1.23 d (6.3) 14 13, 14
16 16.4, CH3 1.67 s 11, 12, 13
17 16.2, CH3 1.72 s 6 7, 8, 9
18 10.1, CH3 1.96 s 6 3, 4, 5
19 6.8, CH3 1.84 s 1, 2, 3
20 55.4, CH3 3.93 s 1
a

Data obtained on a Varian 500 MHz instrument in CDCl3.

b

ovlp = overlapped signals.

c

data taken in DMSO.