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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: J Nat Prod. 2019 Jan 2;82(1):154–162. doi: 10.1021/acs.jnatprod.8b00871

Table 3.

NMR Spectroscopic Data (1H 600 MHz, 13C 150 MHz) for Compounds 5 and 6 Recorded in DMSO-d6

5
6
position δC, type δH (J in Hz) δC, type δH (J in Hz)
1 201.9, C 203.4, C
2 34.2, CH2 Hα: 2.66, dt (3.6, 18.6) 35.1, CH2 2.69, m
Hβ: 2.98, m
3 31.9, CH2 Hα: 2.26, td (4.2, 13.2) 31.5, CH2 Hα: 1.91, m
Hβ: 2.32, dt (4.2, 13.2) Hβ: 2.15, m
4 80.5, C 66.3, CH 4.69, dd (3.6, 9.0)
4a 145.8, C 149.6, C
5 99.0, CH 6.62, s 101.1, CH 6.77, s
6 163.3, C 163.2, C
7 117.9, C 118.0, C
8 160.7, C 160.8, C
8a 109.5, C 109.5, C
9 15.1, CH2 2.56, q (7.2) 60.3, CH 5.16, q (6.6)
10 13.1, CH3 1.01, t (7.2) 22.2, CH3 1.41, d (6.6)
11 41.0, CH2 Hα: 2.01, dd (10.2, 13.2)
Hβ: 3.08, dd (8.4, 13.2)
12 67.1, CH 4.77, t (9.0, 9.6)
13 176.3, C
6-
OCH3
56.0, CH3 3.91, s 55.9, CH3 3.88, s
4-OH 5.64, br s
8-OH 13.07, br s 13.18, s
9-OH a
12-OH 6.12, br s
a

Not observed.