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. 2016 Aug 19;21(8):1089. doi: 10.3390/molecules21081089

Table 3.

1H-NMR Data of compounds 47.

Proton 4 5 6 7
3 6.94 s 7.04 s 6.94 s 6.94 s
5 9.45 d (9.5) 9.51 d (9.5) 9.41 d (9.5) 9.41 d (9.5)
6 7.20 dd (9.5, 3.0) 7.24 dd (9.5, 3.0) 7.11 dd (9.5, 3.0) 7.11 dd (9.5, 3.0)
8 7.26 d (3.0) 7.37 d (3.0) 7.14 d (3.0) 7.13 d (3.0)
9 7.59 d (9.5) 7.70 d (9.5) 7.52 d (9.5) 7.50 d (9.5)
10 7.70 d (9.5) 7.74 d (9.5) 7.67 d (9.5) 7.66 d (9.5)
1′ 6.67 d (3.0) 6.20 d (3.0) 6.24 d (3.0) 6.66 d (3.0)
3′ 6.69 dd (9.5, 3.0) 6.65 d (3.0) 6.58 d (3.0) 6.67 dd (9.5, 3.0)
4′ 8.05 d (9.5) 8.02 d (9.5)
5′ 8.07 d (9.0) 8.02 d (9.5)
6′ 6.38 d (3.0) 6.69 dd (9.0,3.0) 6.61 dd (9.5, 3.0) 6.39 d (3.0)
8′ 6.29 d (3.0) 6.68 d (3.0) 6.60 d (3.0) 6.29 d (3.0)
9′ 2.61–2.63 m a 2.59–2.60 m 2.59–2.63 m 2.61–2.63 m a
10′ 2.61–2.63 m a 2.53–2.56 m 2.54–2.58 m 2.61–2.63 m a
4-OCH3 4.12 s 4.16 s 4.12 s 4.12 s
7-OCH3 3.91 s 3.94 s
4′-OCH3 3.81 s 3.75 s
5′-OCH3 3.80 s 3.80 s

1H-NMR data were measured at 500 MHZ in CD3OD for 4, 67, in acetone-d6 for 5, δ in ppm, J in Hz; a overlapped; the number in brackets represented coupling constants.