Table 1.

¹H and ¹³C NMR Data of Compounds 1–4.

Pos.	1		2		3		4
	δC, type	δH (J in Hz)	δC, type	δH (J in Hz)	δC, type	δH (J in Hz)	δC, type	δH (J in Hz)
1	88.2, C	-	86.6, C	-	80.4, C	-	87.3, C	-
2	137.7, C	-	137.5, C	-	134.8, C	-	133.1, C	-
3	140.4, C	-	142.1, C	-	134.0, C	-	137.0, C	-
4	76.0, CH	4.47, bs	75.8, CH	4.52, dd (12.06, 6.5)	80.5, CH	4.80, d (5.9)	75.5, CH	4.47, br s
5	65.0, CH	4.43, d (6.4	64.9, CH	4.47, d (6.5)	67.9, CH	4.33, d (6.0)	66.0, CH	4.47, br s
1’	57.1, CH	4.51, d (7.3)	59.5, CH	4.82, d (6.7)	121.0, CH	6.18, m	120.6, CH	6.17, m
2’	69.5, CH	4.33, p (6.4)	70.0, CH	4.20, m	132.5, CH	5.93, dq (15.7, 6.6)	134.55, CH	6.17, m
3’	20.9, CH3	1.34, d (6.2)	19.8, CH3	1.33, d (6.4)	19.3, CH3	1.81, d (7.2)	19.5, CH3	1.82, d (5.1)
1”	171.9, C	-	171.9, C	-	173.0, C	-	172.1, C	-
2”	54.5, CH3	3.91, s	54.6, CH3	3.92, s	53.9, CH3	3.82, s	54.6, CH3	3.91, s
1-OH	-	4.12 s	-	5.11, s	-	-	-	-
4-OH	-	3.43, d	-	3.47, d	-	-	-	-
2’-OH	-	1.95 s	-	3.10 d	-	-	-	-

^aCDCl₃ (¹H NMR 400 MHz, ¹³C NMR 100 MHz).