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. 2010 Dec 21;15(12):9462–9472. doi: 10.3390/molecules15129462

Table 1.

NMR data for compound 10. a

Position δ H δ C Position δ H δ C
1 119.1 OCH2O 6.46 s 103.0
2 7.65 s 105.7 OCH3 3.94 s 56.0
3 148.2 1′ 5.08 d (6.5) 103.0
4 146.9 2′ 3.92 dd (8.5, 6.5) 81.0
4a 109.0 3′ 3.54 t (8.5) 75.8
4b 127.9 4′ 3.47 t (8.5) 69.4
5 8.26 dd (8.5, 1.0) 118.4 5′ 3.18 m 76.9
6 7.56 dd (8.0, 8.5) 126.1 6′α, 6′β 3.8 − 3.6 m 60.5
7 7.23 dd (8.0, 1.0) 110.8 1″ 4.65 d (7.5) 102.4
8 157.2 2″ 3.06 dd (7.5, 8.5) 74.1
8a 120.0 3″ 3.10 t (8.5) 76.1
9 132.6 4″ 3.17 t (8.5) 69.3
10 b 5″ 2.99 ddd (8.5, 4.7, 2.5) 76.4
10a 124.4 6″α, 6″β 3.35 m 60.3
3.8 − 3.6 m
CO 167.4 NH 10.18 s

a The 1H- and 13C-NMR data were assigned with the assistance of gHMQC, gHMBC, and 1H-1H COSY experiments (11.7 T); recorded in DMSO-d6; J in Hz; b Signal not observed.