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. 2013 Dec 30;9:2940–2949. doi: 10.3762/bjoc.9.331

Table 1.

1H and 13C NMR data (500 and 125 MHz, CD3OD) of plakilactones G (1) and H (2).

1 2

position δHa δC HMBC δHa δC HMBC

1 175.9 175.5
2 136.6 136.6
3 7.11 br t (1.5) 153.5 C1, C2, C4, C11 7.12 br t (1.2) 153.0 C1, C2, C4, C11
4 91.9 90.7
5 2.04 d (14.7)
1.64 dd (6.0, 14.7)
36.6 C3, C4, C6, C7, C13, C15
C3, C4, C6, C13, C15
1.95 dd (5.2, 14.7)
1.87 ovl
40.0 C3, C4, C6, C7, C13, C15
C3, C4, C6, C7, C13, C15
6 1.43 ovl 37.4 0.91 ovl 39.5 C4, C7
7 3.33b 75.3 C5, C8, C15 2.50 dd (2.0, 8.0) 63.3 C6, C9, C15
8 3.32b 73.9 C7 2.69 ddd (2.0, 5.6, 7.5) 61.6 C9
9 1.76 m
1.34 m
27.4 C10
C8, C10
1.54 m 26.0 C8, C10
10 1.00 t (7.4) 10.1 C8, C9 0.98 t (7.5) 9.9 C8, C9
11 2.28 q (7.5) 19.2 C1, C2, C3, C12 2.26 q (7.5) 19.3 C1, C2, C3, C12
12 1.17 t (7.5) 12.1 C2, C11 1.16 t (7.5) 12.3 C2, C11
13 1.85 m 32.1 C3, C4, C5, C14 1.86 ovl, 1.84 m 31.8 C5, C14
14 0.81 t (7.5) 7.8 C4, C13 0.81 t (7.3) 7.8 C4, C13
15 1.43 ovl 26.2 C6 1.44 m
1.39 m
26.9 C5, C6, C7, C16
C5, C6, C7, C16
16 0.85 t (6.8) 11.6 C6, C15 0.91 t (7.5) 11.8 C6, C15

aCoupling constants are in parentheses and given in Hertz. 1H and 13C assignments aided by COSY, HSQC and HMBC experiments. bOverlapped with solvent signal; ovl: overlapped with other signals.