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. Author manuscript; available in PMC: 2016 Oct 8.
Published in final edited form as: J Nat Prod. 2015 May 19;78(6):1437–1441. doi: 10.1021/np500974f

Table 1.

NMR Spectral Data of Lumiquinone A (1) in Chloroform-d1 (δH 7.25, δC 77.1)

no. δCa type δHb mult (J in Hz) HMBC
1 181.8 C
2 145.6 C
3 105.1 C
4 179.1 C
5 153.1 C
6 120.5 C
7 118.2 CH 6.84 d (16.7) C-2, C-4, C-8, C-9
8 132.4 CH 7.15 d (16.7) C-3, C-10, C-14
9 137.3 C
10 126.2 CH 7.46 d (7.9) C-8, C-12, C-14
11 128.6 CH 7.34 t (7.3) C-9, C-13
12 127.8 CH 7.26 mc C-10, C-14
13 128.6 CH 7.34 t (7.3) C-9, C-11
14 126.2 CH 7.46 d (7.9) C-8, C-10, C-12
15   24.1 CH 3.17 m C-1, C-5, C-6, C-16, C-17
16   19.8 CH3 1.23 d (7.1) C-6, C-15, C-17
17   19.8 CH3 1.23 d (7.1) C-6, C-15, C-16
a

Chemical shifts of 13C were determined by HSQC and HMBC.

b

600 MHz.

c

Overlapping signal.