Skip to main content
. 2019 Nov 21;45(1):98–107. doi: 10.1016/j.jgr.2019.11.007

Table 1.

NMR data of acremonidin E (1, DMSO-d6)a

No. δc, mult.b δH (J in Hz) COSY HMBC
1 167.9, qC
2 112.3, qC
3 141.2, CH
4 117.4, CH 6.93, d (J = 8.8 Hz) 5 2
5 122.1, CH 6.81, d (J = 8.8 Hz) 4 3,7
6 146.5, CH
7 131.1, qC
8 199.9, qC
9 108.9, qC
10 162.2, CH 12
11 107.4, qC 6.11, s 15
12 147.4, qC
13 107.4, CH 6.11, s 15
14 162.2, CH 12
15 22.3, CH3 2.17, s
16 52.5, OCH3 3.55, s 1
3-OH 11.37, br s
6-OH 11.37, br s
10-OH 9.20, br s
14-OH 9.70, br s
a

300 MHz for 1H NMR and 125 MHz for 13C NMR.

b

Multiplicity was determined by analysis of 2D spectra.