Table 2 NMR (500 MHz, methanol-d4) data for angiolactone (1)

From: Angiolactone, a new Butyrolactone isolated from the terrestrial myxobacterium, Angiococcus sp.

Pos

δH, mult (J in Hz)

δCa

COSY

HMBC

1

 

175.1

  

2

2.83, dd (7.9, 6.7)

52.2

7

1, 3, 6, 7, 8

3

 

80.8

  

4

 

153.2

  

5

5.25, s

105.8

 

3, 4, 2′, 6′

6a

2.96, d (13.6)

41.2

 

2, 3, 4, 1′′, 2′′, 6′′

6b

2.65, d (13.6)

  

2, 3, 4, 1′′, 2′′, 6′′

7

1.82, m

22.8

2, 8a/b

1, 2, 3, 8

8a

1.61, m

37.8

7, 8b

 

8b

1.48, m

 

7, 8a, 9

 

9

1.65, m

29.1

8b, 10, 11

 

10

0.98b, d (6.4)

22.8

9

8, 9, 11

11

0.97b, d (6.4)

22.8

9

8, 9, 10

1′

 

135.2

  

2′

7.40, d (7.6)

129.4

3′

5, 4′, 6′

3′

7.27, dd (7.6, 7.0)

129.1

2′, 4′

1′, 5′

4′

7.17, dd (7.2, 7.0)

127.6

3′, 5′

2′, 6′

5′

7.27, dd (7.6, 7.2)

129.1

4′, 6′

1′, 3′

6′

7.40, d (7.6)

129.4

5′

5, 2′ 4′

1′′

 

127.5

  

2′′

7.00, d (8.3)

132.8

3′′

6, 4′′, 6′′

3′′

6.63, d (8.3)

115.3

2′′

1′′, 4′′, 5′′

4′′

 

157.4

  

5′′

6.63, d (8.3)

115.3

6′′

1′′, 3′′, 4′′

6′′

7.00, d (8.3)

132.8

5′′

6, 2′′, 4′′

  1. a13C NMR resonances obtained from 2D HSQC and HMBC experiments.
  2. bOverlapping signals.