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. Author manuscript; available in PMC: 2016 Jun 30.
Published in final edited form as: Bioorg Med Chem. 2006 Oct 11;14(24):8495–8505. doi: 10.1016/j.bmc.2006.08.042

Table 9.

1H and 13C NMR spectral data for compounds 15, 16, and 17

Position 15
16
17
δH δC δH δC δH δC
2 7.1, br d 131.4, d 6.9, d(6) 132.1, d 7.0, br d 131.5, d
3 6.8, br d 101.0, d 6.8, d(6) 101.2, d 6.8, br d 113.4, d
3a 149.2, s 149.4, s 149.2, s
5 7.6, d(6) 147.0, d 8.0, d(7.6) 146.4, d 7.5, br d 147.0, d
6 7.5, br d 118.3, d 7.2, d(7.6) 113.4, d 7.5, br d 124.8, d
6a 136.7, s 135.5, s 136.5, s
7 6.8, s 101.0, d 6.7, s 101.1, d 6.8, s 100.7, d
8 151.6, s 157.2, s 158.5, s
9 135.0, s 135.0, s 135.0, s
9a 123.8, s 123.9, s 124.0, s
9b 117.9, s 118.1, s 118.0, s
NCH3 3.9, s 45.3, q 3.8, s 45.4, q 3.9, s 45.5, q
OCH3 3.9, s 56.8, q 3.9, s 56.7, q 3.9, s 56.8, q
1′ 163.2, s 164.9, s 164.9, s
2′ 125.0, s 125.3, s 125.2, s
3′ 8.0, br d 127.8, d 8.1, d(8) 130.5, d 8.1, d(8) 130.5, d
4′ 7.4, dd(8) 113.6, d 7.3, d(8) 129.7, d 7.6, d(8) 126.0, d
5′ 157.2, s 145.5, s 157.3, s
6′ 149.0, s 7.3, d(8) 129.7, d 7.6, d(8) 126.0, d
7′ 8.0, br d 118.1, d 8.1, d(8) 130.5, d 8.1, d(8) 130.5, d
8′ 2.5, s 21.8, q 35.3, s
9′ 1.4, s 31.0, q
10′ 1.4, s 31.0, q
11′ 1.4, s 31.0, q

Measured in CDCl3 at 400 MHz for 1H and 100 MHz for 13C, respectively. J values in Hz.