Skip to main content
. Author manuscript; available in PMC: 2019 Apr 27.
Published in final edited form as: J Org Chem. 2018 Oct 26;83(22):13670–13677. doi: 10.1021/acs.joc.8b01609

Table 2.

1H and13C NMRa data for lepadin J (2) (TFA salt, CDCl3, 23˚ C)

Position 1H (mult, J)a 13C (mult)b COSY HMBC
1 8.03, brs 2, 8a
2 3.53, m 54.0 (CH) 1, 9
3 5.07, m 68.4 (CH) 2, 4 4a
4 3.12, m; 2.12, m
31.1 (CH2) 4a, 5
4a 117.3 (C)
5 142.4 (C)
6 2.01, m; 1.85, m 32.8 (CH2) 7
7 1.30, m 22.4 (CH2) 6
8 2.05, m; 1.77, m 26.4 (CH2) 8a 4a
8a 3.73, m 55.3 (CH) 8
9 1.29, m 14.6 (CH3) 1, 2
1” 164.3 (C)
2” 5.74, d (14.8) 111.3 (CH) 3” 1”
3” 8.08, dd (14.8, 1.5) 149.8 (CH) 2” 1”, 2”, 5”
4”
5” 2.33, d (1.5) 13.6 (CH3)
1’ 2.02, m; 1.85, m 27.1 (CH2)
2’ 1.31, m; 1.20, m 27.9 (CH2)
3’ 1.24, mc 29.3 (CH2)c
4’ 1.24, mc 29.3 (CH2)c
5’ 1.38, m; 1.27, mc 25.2 (CH2)c
6’ 1.40, m 37.1 (CH2) 7’
7’ 3.57, m 71.2 (CH) 6’, 8’
8’ 1.41, m 39.3 (CH2) 7’
9’ 1.43, m; 1.33, m 18.5 (CH2) 10’
10’ 0.91, t (6.7) 13.6 (CH3) 9’ 8’, 9’
NH 8.23, bs
a

, 600 MHz.

b

, 150 MHz, multiplicities assigned by edited HSQC.

c

, interchangeable assignments.