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Table 2 13C and 1H chemical shifts assignments for the compound

From: A bioactive flavonoid from Pavetta crassipes K. Schum

Position

13C (400 MHz, DMSO-d6)

1H (400 MHz, DMSO-d6)

2

156.4

 

3

133.2

 

4

177.3

 

5

156.6

12.62 (1H, s, 5-OH)

6

98.6

6.19 (1H, d, J = 1.88)

7

164.0

 

8

93.6

6.41 (1H, d, J = 1.80)

9

161.1

 

10

103.9

 

1'

121.1

 

2'

115.2

7.53 (1H, d, J = 8.08)

3'

144.6

 

4'

148.3

 

5'

116.2

6.85 (1H, d, J = 7.84)

6'

121.6

7.55 (1H, d, J = 7.56)

1G

101.1

5.32 (1H, d, J = 7.44)

2G

73.9

3.08 (1H, d, J = 9.28)

3G

75.8

3.23 (1H, d, J = 6)

4G

69.9

3.26-3.36 (3H)

5G

76.3

3.21 (1H, d, J = 5.52)

6G

66.9

3.26-3.36 (3H)

1R

100.7

4.37 (1H, d, J = 7.6)

2R

70.3

3.04 (1H, d, J = 2.68)

3R

70.5

3.69 (1H, d, J = 10.4)

4R

71.8

3.26-3.36 (3H)

5R

68.2

3.39 (1H, d, J = 1.76)

6R

17.6

0.97 (3H, d, J = 6.12)