Table 5 13C NMR data (acetone-d6, 125 MHz) of compounds 1, 3 and 4
From: Herbicidal secondary metabolites from Bacillus velezensis JTB8-2 against Orobanche aegyptiaca
Carbon | 1 | 3 | 4 |
|---|---|---|---|
δC, type | δC, type | δC, type | |
1 | 165.9, C | 165.9, C | 171.3, C |
3 | 45.6, CH2 | 53.8, CH2 | 54.0, CH2 |
4 | 23.1, CH2 | 68.3, CH | 68.8, CH |
5 | 28.9, CH2 | 40.7, CH2 | 38.1, CH2 |
6 | 59.6, CH | 59.4, CH | 54.8, CH |
7 | 169.9, C | 168.9, C | 167.3, C |
9 | 57.1, CH | 56.7, CH | 58.2, CH |
10 | 37.0, CH2 | 38.1, CH2 | 39.3, CH2 |
11 | 25.4, CH | ||
12 | 23.3, CH3 | ||
13 | 22.1, CH3 | ||
1' | 138.2, C | 137.3, C | |
2' | 129.2, CH | 129.2, CH | |
3' | 130.6, CH | 130.9, CH | |
4' | 127.5, CH | 127.8, CH | |
5' | 130.6, CH | 130.9, CH | |
6' | 129.2, CH | 129.2, CH |