Table 3 1H NMR and 13C NMR Spectroscopic Data for Compounds 5–6 and 8–9.

From: Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis

Proton No.

5 a

Proton No.

6 b

Proton No.

8 a

Proton No.

9 a

δH multi

δC

δH

δC

δH

δC

δH

δC

2

 

87.0

2

 

85.0

2

 

87.0

2

 

87.0

3

3.86 d (8.5)

61.8

3

4.09 d (8.5)

62.2

3

3.88 d (8.5)

61.8

3

3.88 d (8.5)

62.0

4

4.06 d (8.5)

61.8

4

3.91 d (8.5)

62.5

4

4.10 d (8.5)

62.0

4

4.12 d (8.5)

61.8

5

 

83.6

5

 

88.0

5

 

83.3

5

 

83.4

5a

 

106.1

5a

 

107.6

5a

 

106.1

5a

 

106.2

6

 

159.0

6

 

154.2

6

 

159.0

6

 

159.0

7

5.78 d (2.0)

93.0

7

6.04 d (2.0)

95.0

7

6.04 d (2.0)

93.0

7

5.77 d (2.0)

92.9

8

 

161.2

8

 

162.7

8

 

161.2

8

 

161.2

9

6.03 d (2.0)

94.0

9

5.89 d (2.0)

93.6

9

5.78 d (2.0)

94.0

9

6.03 d (2.0)

93.9

9a

 

153.0

9a

 

160.4

9a

 

153.0

9a

 

153.0

10

4.89 s

78.8

10

4.68 s

79.7

10

4.89 s

79.0

10

4.87 d (5.0)

78.9

11

 

173.6

11

 

175.8

11

 

173.8

11

 

173.3

13

2.75 m 2.85 m

39.1

13

2.91 m 2.83 m

40.2

13

2.96 m 2.86 m

39.1

13

2.90 m 2.85 m

39.5

14

0.94 m

26.4

14

1.15 m

27.3

14

1.36 m

24.2

14

1.18 m

29.7

15

1.01 m

26.1

15

1.28 m

27.6

15

1.94 t (7.3)

31.3

15

1.10 m

25.7

16

2.95 m

39.3

16

3.17m

40.4

16

 

173.4

16

3.40 m

62.5

18

 

172.0

18

 

170.0

COOCH3

3.62

51.7

5-OH

5.44 s

 

19

3.45 s

43.1

19

 

126.7

   

10-OH

5.18 d (5.0)

 

20

 

126.8

20, 24

7.67 d (8.5)

130.4

      

21, 25

7.06 d (8.5)

130.8

21, 23

6.81 d (8.5)

114.4

      

22, 24

6.84 d (8.5)

116.5

22

 

161.9

      

23

 

155.6

         

6-OMe

3.09 s

55.9

6-OMe

3.10 s

56.4

6-OMe

3.08 s

55.9

6-OMe

3.07 s

55.9

8-OMe

3.71 s

55.5

8-OMe

3.71 s

55.8

8-OMe

3.71 s

55.5

8-OMe

3.69 s

55.5

4′-OMe

3.78 s

55.5

4′-OMe

3.76 s

55.8

4′-OMe

3.82 s

55.4

4′-OMe

3.81 s

55.5

NH-12

5.50 t (5.5)

 

NH-12

5.25 t (5.5)

 

NH-12

6.58 m

 

NH-12

6.74 t (6.0)

 

NH-17

6.68 t (5.5)

 

NH-17

6.47 t (5.5)

       

1′

 

130.3

1′

 

131.7

1′

 

130.1

1′

 

130.3

2′6′

7.68 d (8.5)

129.4

2′6′

7.69 d (8.5)

130.2

2′6′

7.71 d (8.3)

129.3

2′6′

7.74 d (8.6)

129.4

3′5′

6.86 d (8.5)

113.9

3′5′

6.90 d (8.5)

116.1

3′5′

6.92 d (8.3)

114.0

3′5′

6.92 d (8.6)

114.0

4′

 

159.8

4′

 

161.1

4′

 

159.9

4′

 

159.8

1″

 

136.9

1″

 

138.3

1″

 

136.8

1″

 

137.0

2″6″

6.97 m

128.7

2″6″

6.97 m

129.8

2″6″

6.97 m

128.7

2″6″

6.98 m

128.7

3″5″

7.16 m

128.0

3″5″

7.17 m

128.8

3″5″

7.17 m

127.9

3″5″

7.14 m

127.9

4″

7.16 m

127.3

4″

7.17 m

128.2

4″

7.17 m

127.3

4″

7.14 m

127.2

  1. a,b 1H NMR spectra measured at 500 MHz; 13C NMR spectra measured at 125 MHz; a was obtained in CDCl3; b was obtained in methanol-d4. The assignments are based on the 2D-NMR spectra.