Table 2.

¹H and ¹³C NMR Spectroscopic Data for Compounds 6 and 7

	amomol A (6)		amomol B (7)
position	δC, mult.a	δH (J in Hz)	δC, mult.a	δH (J in Hz)
2	111.6, qC		111.5
3	36.6, CH2	2.34, m	36.6	2.24, m
		2.15, m
4	34.9, CH2	2.39, m	35.1	2.43, m
		2.07, m		2.07, m
5	79.1, qC		78.7
6	148.4, CH	6.78, d (10.0, 2.7)	148.2	6.81, d (10.0)
7	127.1, CH	6.13, d (10.0)	127.4b	6.14, d (10.0)
8	185.2, qC		185.3
9	127.7, CH	6.17, d (10.0)	127.5b	6.17, d (10.5)
10	150.6, CH	6.85, d (10.0, 2.7)	150.6	6.85, d (10.5)
11	40.7, CH2	2.13, m	40.1	1.96, m
		1.70, brd (14.7)		1.96, m
12	69.1, CH	3.84, m	68.2	3.79, m
13	37.8, CH2	1.54, m	37.8	1.53, m
		1.43, m		1.43, m
14	25.4, CH2	1.43, m,	25.5	1.43, m
		1.33, m		1.33, m
15–24	29.6–29.7, CH2	1.26–1.33, m	29.6–29.7	1.26–1.33, m
25	31.9, CH2	1.26, m	31.9	1.26, m
26	22.7, CH2	1.30, m	22.7	1.30, m
27	14.1, CH3	0.88, t (6.8)	14.1	0.89, t (6.7)
OCH3	48.9, CH3	3.35, s	48.5	3.35, s

^aMultiplicity was deduced from the DEPT and HSQC spectroscopic data.

^bAssignments are interchangeable.