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. 2019 Jun 12;7:435. doi: 10.3389/fchem.2019.00435

Table 2.

1H (600MHz) and 13C (150MHz) NMR data of 5 (CDCl3).

Position δC, type δH, mult. (J in Hz)
1 45.5, CH 3.60, d (3.5)
2 74.2, C
3 209.2, C
4 62.5, C
5 194.9, C
6 104.7, C
7 172.3, C
8 117.2, CH 6.12, d (14.9)
9 144.6, CH 7.38, dd (14.8, 10.2)
10 130.8, CH 6.29, dd (15.3, 10.2)
11 141.4, CH 6.24, m
12 19.0, CH3 1.91, d (6.0)
13 24.4, CH3 1.28, s
14 10.4, CH3 1.23, s
1′ 76.3, CH 5.44, dd (8.9, 3.5)
2′ 41.4, CH 2.89, ddd (11.5, 8.9, 5.5)
3′ 30.2, CH2 2.70, dd (19.2, 11.6)
2.24, dd (19.2, 5.4)
4′ 174.8, C
7-OH 14.32, s