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. 2017 Sep 20;7:11956. doi: 10.1038/s41598-017-12327-1

Table 1.

1H NMR data for compounds 16 in CDCl3 (δ in ppm, J in Hz).

Pos. 1b 2b 3a 4 a 5a 6a
2 6.66, s 6.07, s 6.17, s 6.24, s 6.60, s 6.20, s
3 3.15, m 3.18, m 3.17, m 3.17, m 3.17, m 3.16, m
4 2.58, m 2.58, m 2.62, m 2.70, m 2.59, m 2.77, dd (2.4, 5.6)
5 2.58, m 2.61, m 2.55, m 2.56, m 2.59, m 2.56, m
7 5.35, s 5.37, brs 5.37, brs 5.44, brs 5.45, brs 5.43, brs
8 3.00, d (10.8) 3.05, d (10.2) 2.97, brd (9.2) 3.08, d (10.8) 3.21, m 3.06, d (10.4)
10a 1.15, m 1.16, m 1.18, m 1.16, m 1.17, m 1.18, m
10b 1.30, m
11 1.18, d (7.2) 1.21, d (6.6) 1.21, d (6.8) 1.22, d (7.2) 1.21, d (6.6) 1.24, d (7.2)
12 1.72, s 1.75, s 1.74, s 1.76, s 1.76, s 1.77, s
13 6.23, d (10.8) 6.25, d (10.8) 6.23, d (10.2) 6.19, d (10.8) 6.06, d (11.0) 6.19, d (11.2)
15a 2.17, d (12.6) 2.15, d (10.8) 2.16, brd (11.4) 1.98, m 1.88, m 1.95, m
15b 1.80, t (12.0, 24.0) 1.80, t (12.0, 24.6) 1.89, m 1.87, m 1.76, m 1.85, m
16 2.58, m 2.59, m 2.55, m 1.87, m 1.76, m 1.85, m
17a 2.60, m 2.56, m 2.78, m 1.98, m 1.98, m 1.95, m
17b 2.21, d (15.0) 2.30, d (16.0) 2.55, m 1.87, m 1.88, m 1.85, m
18 3.76, m 3.60, m 3.60, m
19a 2.76, m 5.01, dd (2.4, 10.8) 4.57, brd (8.0) 1.39, m 3.09, m 3.42, m
19b 1.87, m
20a 3.85, ddd (2.4, 11.4, 17.4) 2.92, m 4.16, dd (11.1, 17.4) 3.60, m 4.11, dd (2.2, 18.7) 4.20, d (17.6)
20b 2.40, ddd (,2.4, 7.8, 17.4) 2.55, m 1.92, m 1.93, m 1.90, m
22 1.58, m 1.56, m 1.54, m 1.55, m 1.58, m 1.54, m
23/24 0.90, d (6.6) 0.90, d (6.6) 0.91, d (6.0) 0.89, d (6.8) 0.90, d (6.6) 0.90, d (6.8)
25 1.36, s 1.35, s 1.43, s 1.55, s 1.53, s 1.54, s
26a 3.58, dd (4.8, 10.8) 3.61, dd (5.4, 10.8) 3.66, m 3.60, m 3.55, m 3.56, m
26b 3.41, dd (6.0, 9.6) 3.45, dd (7.2, 10.8) 3.53, t (7.3, 17.0) 3.35, m 3.33 t (9.2, 18.5) 3.34, t (9.2, 18.4)
27 3.34, s 3.51, s

aSpectra were recorded at 400 MHz. bSpectra were recorded at 600 MHz.