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. 2021 Nov 10;26(22):6798. doi: 10.3390/molecules26226798

Table 2.

Spectrum data for compound 8f.

1H NMR 1H-1HCOSY Assignment
13.41 (bs; 1H) OH-4/4’
12.91 (bs; 1H) OH-4’/4
12.20 (s; 2H) 6.81 NH-1/1’, 1″
12.09 (bs; 1H) NH-1’/1
8.84 (s; 1H) H-d
7.47 (d, J = 8.3; 1H) 7.38, 7.22 H-7″
7.40 (d, J = 9.2; 2H) 7.26 H-8, 8’
7.38 (d, J = 8.4; 2H) 7.47, 7.26, 2.29 H-5/5’, 8″
7.33 (m; 1H) 7.26 H-5’/5
7.26 (d, J = 8.1; 2H) 7.40, 7.38, 7.33 H-7, 7’
7.22 (s; 1H) 7.47, 2.29 H-5″
7.05 (d, J = 8.2; 2H) 7.01, 6.15 H-o
7.01 (d, J = 8.2; 2H) 7.05 H-m
6.81 (s; 1H) 12.20 H-3″
6.15 (bs; 1H) 7.05 H-a
5.27 (s; 2H) H-b
3.82 (s; 6H) H-6b, 6b’
2.29 (s; 3H) 7.40, 7.38, 7.26 H-6a″
13C NMR HSQC HMBC Assignment
165.85, 164.13 6.15 C-2, 2’
161.84 C-4, 4’
160.84 C-2″, 4″
156.06 7.05, 5.27 C-p
154.81 7.40, 3.82 C-6, 6’
143.42 8.84, 7.40, 7.22, 6.81, 5.27 C-c
137.50 7.47, 7.22 C-8a″
133.15 7.47 7.47, 7.22 C-7″
131.73, 131.51 7.38, 7.26, 2.29 C-8a, 8a’
130.07 C-i
127.40 7.05 C-o, 6″
126.50 8.84 8.84,3 7.01, 5.27 C-d
123.15 7.22 7.47, 7.05, 2.29 C-5″
120.82 7.26 7.01 C-7, 7’
117.69 6.81 7.05, 6.813 C-3″
117.45 7.40 7.403 C-8, 8’
116.69 7.38, 7.33 C-4a, 4a’
115.89 7.38 C-8″
114.38 7.01 7.38, 6.81 C-m, 4a″
111.86, 110.18 6.15 C-3, 3’
103.81 7.38, 7.33 C-5, 5’
60.85 5.27 C-b
55.40 3.82 3.823 C-6b, 6b’
34.71 6.15 C-a
20.50 2.29 7.47, 7.22, 2.293 C-6a″
15N NMR HSQC HMBC Assignment
247.4 8.84, 6.81 N-e
151.6 12.20 7.38, 6.81 N-1″
144.2 12.09 N-1’/1
142. 12.20 N-1/1‘
N-f, g n/o.