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. 2021 Nov 1;11(55):34938–34944. doi: 10.1039/d1ra07196c

1H and 13C NMR data of 1–3.

Pos. 1 2 3
δ H a (multi, J in Hz) δ C b , e, type δ H a (multi, J in Hz) δ C b , e, type δ H c (multi, J in Hz) δ C d , e, type
1 172.1, C 172.2, C 172.1, C
3 5.27, br s (2H) 70.2, CH2 5.27, br s (2H) 70.2, CH2 5.27, br s (2H) 70.2, CH2
3a 148.8, C 148.8, C 148.8, C
4 122.7, C 122.8, C 122.7, C
5 164.6, C 164.6, C 164.6, C
6 130.9, C 130.9, C 130.9, C
7 153.8, C 153.9, C 153.8, C
7a 113.2, C 113.2, C 113.2, C
Me-4 2.21, s (3H) 11.6, CH3 2.22, s (3H) 11.6, CH3 2.21, s (3H) 11.6, CH3
MeO-5 3.79, s (3H) 61.6, CH3 3.80, s (3H) 61.5, CH3 3.79, s (3H) 61.6, CH3
1′ 3.45, m 25.0, CH2 3.45, m 25.0, CH2 3.45, m 25.0, CH2
3.65, dd (14.3, 6.5) 3.69, dd (14.0, 7.3) 3.65, dd (14.2, 7.2)
2′ 5.28, t (6.5) 124.9, CH 5.26, t (7.3) 124.3, CH 5.28, t (7.2) 124.9, CH
3′ 134.9, C 136.6, C 134.9, C
4′ 2.28, t (7.4, 2H) 36.0, CH2 2.00, t (7.4, 2H) 40.6, CH2 2.28, t (7.5, 2H) 36.0, CH2
5′ 2.34, t (7.4, 2H) 35.5, CH2 2.08, m (2H) 35.9, CH2 2.41, t (7.5, 2H) 35.5, CH2
6′ 178.2, C 5.09, t (7.4) 125.5, CH 176.9, C
7′ 1.82, d (1.2, 3H) 16.5, CH3 134.8, C 1.82, d (1.2, 3H) 16.5, CH3
6′-OMe 3.57, s (3H) 52.0, CH3
8′ 2.18, m (2H) 34.0, CH2
9′ 2.16, m (2H) 35.6, CH2
10′ 179.0, C
11′ 1.57, d (1.3, 3H) 16.1, CH3
12′ 1.80, d (1.3, 3H) 16.5, CH3
1′′ 5.33, d (7.7) 106.5, CH 5.29, d (7.7) 106.7, CH 5.33, d (7.7) 106.5, CH
2′′ 3.50, m 75.8, CH 3.53, m 75.9, CH 3.50, m 75.8, CH
3′′ 3.23, ddd (9.7, 5.5, 2.3) 78.5, CH 3.22, ddd (9.8, 5.4, 2.2) 78.5, CH 3.23, ddd (9.7, 5.5, 2.3) 78.4, CH
4′′ 3.37, dd (9.8, 8.8) 71.4, CH 3.37, t (9.0) 71.4, CH 3.37, dd (9.8, 8.8) 71.4, CH
5′′ 3.46, t (9.0) 78.4, CH 3.45, t (9.0) 78.4, CH 3.46, t (9.0) 78.4, CH
6′′ 3.65, m 62.6, CH2 3.64, m 62.7, CH2 3.65, m 62.6, CH2
3.76, m 3.78, m 3.76, m
a

Measured in methanol-d4 at 600 MHz.

b

Measured in methanol-d4 at 150 MHz.

c

Measured in methanol-d4 at 400 MHz.

d

Measured in methanol-d4 at 100 MHz.

e

Assigned based on gHMQC and gHMBC spectra.