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Table 1 1H NMR (600 MHz) and 13C NMR (150 MHz) spectral data of compounds 13 in DMSO-d 6

From: Dihydroisocoumarins from Radix Glycyrrhizae

Position

Compound 1

Compound 2

Compound 3

δ C

δH (J in Hz)

δ C

δH (J in Hz)

δ C

δH (J in Hz)

1

169.8

167.6

168.0

2

3

78.5

4.72 (1H, qd, 6.4, 1.6)

80.7

4.88 (1H, qd, 6.8, 1.6)

80.9

4.87 (1H, qd, 6.8, 1.2)

4

62.3

4.66 (1H, dd, 6.8, 1.6)

63.2

4.77 (1H, dd, 5.2, 1.6)

63.6

4.67 (1H, dd, 5.6, 1.2)

5

124.7

125.3

127.0

6

138.3

7.64 (1H, d, 8.8)

138.3

7.66 (1H, d, 8.8)

137.1

7.45 (1H, d, 8.4)

7

117.3

6.99 (1H, d, 8.8)

117.0

7.03 (1H, d, 8.8)

116.7

6.92 (1H, d, 8.4)

8

161.1

160.6

158.8

9

16.6

1.45 (3H, d, 6.4)

17.4

1.16 (3H, d, 6.8)

16.7

1.16 (3H, d, 6.8)

10

62.2

5.09 (1H, d, 12.4)

62.0

5.07 (1H, d, 12.4)

17.6

2.29 (3H, s)

  

5.17 (1H, d, 12.4)

 

5.20 (1H, d, 12.4)

  

11

170.8

170.2

   

12

21.2

2.04 (3H, s)

20.7

2.03 (3H, s)

  

4a

141.3

138.9

138.6

 

8a

108.2

107.4

107.1

 

OH-4

 

5.70 (1H, d, 7.2)

 

5.96 (1H, d, 5.2)

5.82 (1H, d, 5.2)

OH-8

 

11.20 (1H, s)

 

11.19 (1H, s)

10.9 (1H, s)

  1. Chemical shift values are expressed in ppm