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Table 1 NMR data related to compounds 2 and 3 (1H at 300 MHz, CDCl3)

From: A novel cytosporone 3-Heptyl-4,6-dihydroxy-3H-isobenzofuran-1-one: synthesis; toxicological, apoptotic and immunomodulatory properties; and potentiation of mutagenic damage

Hydrogen

Compound

2a

δ(ppm) (m/J Hz)

3b

δ(ppm) (multiplicity/J Hz)

3

5,41 (dd/J1 = 8,0/J2 = 2,9)

5,45 (dd/J 1  = 7,8/J 2  = 3,0)

5

6,63 (d/1,9)

6,68 (d/1,8)

7

6,87 (d/1,9)

6,72 (d/1,8)

10

2,16 e 1,61 (m)

2,22 e 1,70 (m)

11

1,22 (m)

1,25-1,31 (m)

12

1,22 (m)

1,25-1,31 (m)

13

1,22 (m)

1,25-1,31 (m)

14

1,22 (m)

1,25-1,31 (m)

15

1,28

1,25-1,31 (m)

16

0,83 (t/J = 6,9)

0,84 (t/J = 6,3)

C-4-OCH3

3,82 (s)

-

C-6-OCH3

3,83 (s)

-

Ph-OH

-

9,28 e 8,96 (sl)

  1. aSolubilized in CDCl3. bSolubilized in Acetone-d6