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. 2014 Nov 20;12(11):5563–5575. doi: 10.3390/md12115563

Table 2.

1H and 13C NMR data for compounds 46.

NO. 4 c 5 d 6 c
δH (J in Hz) δC δH (J in Hz) δC δH (J in Hz) δC
1 12.03, s
2 8.41, s 134.8 152.2 153.0
3 114.1 157.2 8.44, d (4.1) 143.3
3a 125.9
4 8.21, dd (2.0, 6.6) 121.4
5 7.19, m 121.9 153.9 153.0
6 7.23, m 122.9 8.25, s 141.7 8.44, d (4.1) 143.3
7 7.49, dd (1.7, 6.8) 112.2 3.10, t (7.2) 29.3 2.96, t (7.3) 29.2
7a 136.3
8 195.5 2.79, t (7.2) 32.9 2.67, t (7.3) 32.2
9 4.69, t (4.5) 75.8 177.1 173.8
10 3.63, dd (5.5, 11.1)
3.71, dd (4.5, 11.1)
65.3 3.04, t (7.2) 30.7 2.96, t (7.3) 29.2
11 2.76, t (7.2) 33.9 2.67, t (7.3) 32.2
12 176.9 173.8
13 2.88, q (7.5) 28.3
14 1.29, t (7.5) 13.1

c Measured in DMSO-d6 on a Bruker AM-400 spectrometer; d measured in CD3OD on a Bruker DRX-600 spectrometer.