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. 2021 Jun 15;11(34):21153–21169. doi: 10.1039/d1ra03276c

13C NMR data (100 MHz) of compounds 5–9a.

Position 5b 6b 7b 8c 9b
1 144.0 147.9 154.3 150.6 150.0
1a 119.0 127.1 110.4 115.3 129.8
1b 126.5 129.0 123.3 119.9 133.8
2 148.9 153.1 148.3 147.7 145.4
3 107.6 117.6 102.7 143.7 123.8
3a 127.5 128.5 137.9 132.6 131.9
4 29.7 27.7 125.8 107.9 31.4
5 55.0 43.4 144.9 156.6 43.5
6a 63.9 54.9 147.1 132.6 52.7
7 27.5 36.1 184.1 174.7 35.0
7a 123.3 135.7 126.3 126.9 138.4
8 143.5 129.6 152.0 108.1 129.9
9 146.6 129.6 157.9 150.8 129.7
10 114.5 129.1 126.3 113.4 129.5
11 120.7 129.9 125.9 123.0 128.7
11a 124.6 133.2 124.9 120.3 132.7
OCH2O 102.4 104.4 102.8
1-OCH3 61.7 61.3
3-OCH3 61.3
5-OCH3 56.2
8-OCH3 61.7
9-OCH3 56.2
graphic file with name d1ra03276c-t7.jpg 22.7
graphic file with name d1ra03276c-t8.jpg 171.4
N–CH3 44.0
graphic file with name d1ra03276c-t9.jpg 21.1
graphic file with name d1ra03276c-t10.jpg 172.5
1′ 103.0
2′ 75.4
3′ 78.8
4′ 71.9
5′ 78.8
6′ 63.1
a

Assignments were based on 1H–1H COSY, HMQC, HMBC, and NOESY experiments; chemical shifts (δ) are given in ppm.

b

Recorded in CDCl3.

c

Recorded in CD3OD.