Table 1. NMR spectroscopic data for compounds 1 and 2 (pyridine-d₅).

Position	1		2
	δC	δH (J in Hz)	δC	δH (J in Hz)
1	77.8	4.57, brs	77.8	4.58, m
2	74.4	4.41, m	74.0	4.41, m
3	72.8	5.03, brs	72.8	5.03, brs
4	68.7	4.31, brs	68.7	4.31, brs
5	78.2		78.2
6	30.5	2.48, d (13.2)	30.5	2.48, d (13.2)
		1.67, m		1.67, m
7	28.8	1.54, m	28.8	1.50, m
		1.14, m		1.10, m
8	35.2	1.71, m	35.2	1.71, m
9	45.7	1.22, m	45.7	1.20, m
10	45.5		45.5
11	21.9	1.58, m	21.9	1.57, m
		1.45, m		1.41, m
12	40.2	1.59, m	40.2	1.58, m
		1.03, m		1.01, m
13	40.9		40.9
14	56.4	1.03, m	56.4	1.01, m
15	32.5	2.03, m	32.5	2.02, m
		1.44, m		1.43, m
16	81.7	4.59, m	81.8	4.58, m
17	63.3	1.81, m	63.4	1.80, m
18	16.8	0.84, s	16.8	0.83, s
19	13.9	1.59, s	13.9	1.58, s
20	42.2	1.96, m	42.2	1.95, m
21	15.3	1.09, d (7.0)	15.3	1.09, d (7.0)
22	109.8		109.8
23	33.5	1.81, m	33.5	1.76–1.79, m
24	29.3	2.70, m	29.3	2.70, m
		2.25, d (11.5)		2.24, d (11.5)
25	144.7		144.7
26	65.4	4.47, d (12.1)	65.4	4.47, d (12.1)
		4.04, d (12.1)		4.04, d (12.1)
27	109.1	4.82, s	109.1	4.81, s
		4.78, s		4.78, s
	2-O-Xyl		2-O-Ara
1	103.5	5.15, d (7.5)	103.4	5.13, d (7.0)
2	75.4	4.08, m	72.8	4.56, m
3	78.7	4.18, m	74.8	4.22, m
4	71.4	4.24, m	69.7	4.36, m
5	67.7	4.40, m	67.3	4.38, m
		3.76, m		3.85, m