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Table 1 1H and13 C NMR Data of compounds 1 and 2 (δ in ppm, data obtained in CDCl3)

From: Antivirus isoindolinone alkaloids with rare oxocyclopenta[f]isoindole frameworks isolated from the stems of flue cured tobacco

No

1

2

δC

δH (J in Hz)

δC

δH (J in Hz)

1

169.5 (C)

 

167.5 (C)

 

2-NH

 

9.07, s

  

3

43.7 (CH2)

4.32, s

45.9 (CH2)

4.16, s

4

156.3 (CH2)

 

156.9 (C)

 

5

125.1 (C)

 

123.8 (C)

 

6

152.7 (C)

 

152.4 (C)

 

7

116.3 (CH)

7.49, s

115.8 (CH)

7.47, s

3a

128.4 (C)

 

125.2 (C)

 

7a

134.4 (C)

 

136.8 (C)

 

8

28.3 (CH2)

2.76, t (5.6)

28.1 (CH2)

2.75, t (5.6)

9

37.2 (CH2)

3.33, t (5.6)

37.2 (CH2)

3.35, t (5.6)

10

206.3 (C)

 

206.4 (C)

 

1′

  

34.2 (CH3)

2.84, s

-OMe

60.3 (CH3)

3.83, s

60.4 (CH3)

3.83, s