TABLE 1.

¹H and¹³C NMR data (DMSO-d ₆) for compounds 1 ^a and 2 ^b .

pos.	1		2
	δ C	δ H (J in Hz)	δ C	δ H (J in Hz)
1	131.4
2	110.7	6.83, d (1.8)	110.7	6.85, d (1.8)
3	147.5		147.5
4	145.9		145.9
5	115.5	6.79, d (8.2)	115.5	6.65, d (8.1)
6	119.4	6.70, dd (8.2, 1.8)	119.8	6.73, dd (8.1, 1.8)
7	80.7	4.25, d (7.2)	80.7	4.21, d (7.3)
8	44.4	2.11, td (7.2, 4.0)	44.1	2.16, m
9	63.4	3.80, m, 3.99, dd (11.1, 4.0)	63.1	4.19, m, 4.26, m
10	63.5	3.26, m, 3.33, m	63.5	3.22, dd (9.5, 7.0), 3.29, m
11	15.2	1.11, t (7.0)	15.2	1.07, t (7.0)
1′	125.5		125.5
2′	111.1	7.29, d (2.0)	111.1	7.30, d (2.0)
3′	147.9		147.9
4′	149.4		149.4
5′	115.2	6.79, d (8.2)	115.2	6.77, d (8.2)
6′	123.2	7.07, dd (8.2, 2.0)	123.2	7.07, dd (8.2, 2.0)
7′	144.9	7.48, d (15.9)	144.9	7.51, d (15.9)
8′	114.3	6.44, d (15.9)	114.3	6.46, d (15.9)
9′	166.5		166.7
1″	128.9		128.9
2″	109.4	6.94, d (2.0)	109.4	6.89, d (1.9)
3″	147.6		147.6
4″	145.8		145.8
5″	115.4	6.67, d (8.1)	115.4	6.79, d (8.2)
6″	119.0	6.74, dd (8.1, 2.0)	119.0	6.71, dd (8.2, 1.9)
7″	131.2	6.27, d (15.3)	131.3	6.17, d (15.1)
8″	125.2	6.08, dd (15.3, 7.6)	124.7	5.96, dt (15.1, 7.0)
9″	30.8	2.30, dt (14.9, 7.6), 2.48, m c	31.4	2.05, dt (14.6, 7.0), 2.14, m
MeO-3	55.5	3.74, s	55.6	3.75, s
MeO-3′	55.7	3.82, s	55.7	3.81, s
MeO-3″	55.4	3.74, s	55.5	3.72, s

^aRecorded at 600 MHz (¹H) and 150 MHz (¹³C).

^bRecorded at 400 MHz (¹H) and 100 MHz (¹³C).

^cOverlapping with solvent peak.