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. Author manuscript; available in PMC: 2009 Oct 16.
Published in final edited form as: Org Lett. 2008 Sep 25;10(20):4681–4684. doi: 10.1021/ol8020176

Table 1.

1H NMR (δ, DMSO-d6,J in Hz in parentheses) data of compounds 3 and 11-14a

compd H-2 H-5 H-12 H-14 & H-18 H-1′ H-3′ & H-7′ H-9 (N) H-2″& H-6″
3 8.92 s 8.75 s 5.51 s 7.33 d (8.7) 5.08 s 7.29 d (8.7) -- --
11 7.87 s 7.53 s -- -- 4.63 dd (15.1, 18.3) 7.19 d (8.6) 9.82 s 6.68 d (8.6)
12 (CDCl3) 7.69 s 7.65 s 5.13 q (14.2) 7.08 d (8.6) 4.72 s 7.33 d (8.6) 9.47 s 6.72 d (8.6)
13 7.83 s 7.50 s -- -- 4.62 dd (15.1, 18.3) 7.20 d (8.72) 9.68 s 6.56 d (9.2)
14 7.85 s 7.50 s -- -- 4.60 dd (15.1, 18.3) 7.22 d (8.72) 9.4 s 5.80 d (H-2″) (8.72)
a

Assignments are based on DEPT, HMQC and HMBC experiments.