Table 1.

¹³C NMR spectroscopic data for saliniquinones A–F (1–6, in CDCl₃)^A

Position	Compound δC
	1	2	3	4	5	6
2	168.9	169.9	169.6	165.6	170.1	171.6
3	109.8	109.0	110.7	108.5	113.0	109.7
4	179.7	179.8	179.7	180.3	178.7	179.4
4a	126.6	126.6	126.3	126.4	126.5	126.3
5	150.2	150.0	150.2	149.6	150.3	150.4
6	124.0	124.0	124.0	123.5	126.0	126.0
6a	136.9	NRB	NRB	NRB	135.9	136.0
7	181.4	181.4	181.1	181.5	181.7	181.9
7a	132.3	132.1	132.0	132.1	132.3	132.1
8	119.9	119.8	119.8	119.5	119.6	119.5
9	137.3	136.9	137.1	136.6	136.8	136.6
10	125.8	125.7	125.6	125.6	125.5	125.4
11	162.8	162.8	162.8	162.7	162.6	162.6
11a	116.8	116.7	116.4	116.6	116.6	116.7
12	187.0	187.1	187.1	187.2	187.6	187.4
12a	121.6	121.5	121.0	121.4	119.5	119.6
12b	156.6	156.6	155.9	156.4	156.5	156.1
13	65.2	65.2	64.9	65.1	24.4	24.1
14	59.6	57.9	75.7	125.7	44.7	72.9
15	14.0	13.7	25.0	12.3	15.8	26.3
16	66.1	67.7	68.7	142.9	74.5	45.2
17	130.9	22.0	133.2	22.7	138.5	131.8
18	123.1	10.4	120.3	13.3	116.4	120.8

^AChemical shifts (δ) in ppm.

^BResonances were not observed.