Table 1 The 1H NMR and 13C NMR spectral data of the compound 1 in methanol-d4.

From: Isolation, purification and identification of biological compounds from Beauveria sp. and their evaluation as insecticidal effectiveness against Bemisia tabaci

No.

1H NMR

13C NMR

No.

1H NMR

13C NMR

1

3.70 (1H, dd, 10.4, 3.6)

4.10 (1H, dd, 10.4, 5.6)

69.7 (t)

19

5.79, 6.09 (each 1H, br s)

125.2 (t)

2

3.98 (1H, m)

54.6 (d)

1′

177.2 (s)

3

4.13 (1H, br dd, 7.5, 7.3)

72.7 (d)

2′

3.97 (1H, m)

73.0 (d)

4

5.50 (1H, ddt, 15.4, 7.3, 1.3)

131.7 (d)

3′

1.54, 1.71 (each 1H, m)

35.9 (t)

5

5.74 (1H, dtd, 15.4, 6.6, 0.7)

133.4 (d)

4′

1.35−1.45 (2H, m)

26.2 (t)

6

2.26−2.33 (2H, m)

28.1 (t)

5′−13′

1.24−1.33 (18H, m)

30.5−30.8 (t)

7

2.82 (2H, br t, 7.4)

38.1 (t)

14′

1.27 (2H, m)

33.1 (t)

8

203.0 (s)

15′

1.30 (2H, m)

23.7 (t)

9

150.2 (s)

16′

0.89 (3H, t, 7.0)

14.4 (q)

10

2.25 (2H, br t, 7.6)

32.0 (t)

1″

4.26 (1H, d, 7.8)

104.7 (d)

11

1.38 (2H, m)

29.8 (t)

2″

3.18 (1H, dd, 9.2, 7.8)

75.0 (d)

12−15

1.24−1.33 (8H, m)

30.5−30.8 (t)

3″

3.35 (1H, dd, 9.2, 8.8)

77.9 (d)

16

1.27 (2H, m)

33.1 (t)

4″

3.27 (1H, m)

71.6 (d)

17

1.30 (2H, m)

23.7 (t)

5″

3.27 (1H, m)

78.0 (d)

18

0.89 (3H, t, 7.0)

14.4 (q)

6″

3.66 (1H, dd, 11.9, 5.5)

3.86 (1H, dd, 11.9, 1.3)

62.7 (t)