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. 2024 Aug 15;14(1):45. doi: 10.1007/s13659-024-00465-9

Table 1.

1H NMR spectroscopic data of silvaticusins A–C (13) (δ in ppm, J in Hz)

No 1a 2a 3b
1a 0.89, m 0.82, m 1.93, overlap
1b 1.27, m 1.15 d, (13.5) 1.65, overlap
2a 1.08, m 1.26, m 1.92, overlap
2b 1.31, m 1.26, m 1.92, overlap
3a 1.23, m 1.09, m 4.04, m
3b 1.23, m 1.34, m
5 1.56, d, (5.3) 1.41, dd, (11.7, 6.9) 1.59, br d, (12.4)
6a 4.21, d, (5.3) 2.04, m 2.16, q, (12.4)
6b 3.57, m 1.74, m
7 4.80, dt, (12.4, 4.7)
9 2.53, dd, (15.3, 6.3) 1.56, m 1.42, overlap
11a 1.79, m 1.99, m 1.43, overlap
11b 1.95, m 1.99, m 1.52, m
12a 4.32, t, (8.2) 4.26, t, (8.2) 1.66, overlap
12b 0.83, m
13 3.18, br s 3.52, br s 3.23, br s
14 5.34, br s 5.59, br s 5.09, br s
15 5.72, br s
17a 5.36, d, (1.9) 5.49, s 6.30, s
17b 5.74, d, (1.9) 6.38, s 5.39, s
18 1.15, s 1.04, s 9.5, s
19 1.05, s 0.77, s 1.39, s
20a 4.07, d, (9.6) 4.09, d, (10.0) 1.07, s
20b 4.12, d, (9.6) 4.31, d, (10.0)

aRecorded on a 500 MHz NMR spectrometer in pyridine-d5. bRecorded on an 800 MHz NMR spectrometer in pyridine-d5