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Table 2 1 H NMR spectroscopic data for compounds 13 (δ in ppm, mult., J in Hz)

From: Chemical constituents from the medicinal herb-derived fungus Chaetomium globosum Km1226

  

1 a

 

2 a

 

3 a

position

 

δH, mult (J in Hz)

 

δH, mult (J in Hz)

 

δH, mult (J in Hz)

1a

 

5.22 dd (16.2, 1.8)

 

1.09 t (7.2)

 

1.10 t (7.2)

1b

 

5.09 dd (10.2, 1.8)

    

2

 

6.36 dt (16.2, 10.2)

 

2.29 qd (7.2, 7.2)

 

2.30 qd (7.2, 7.2)

    

2.29 qd (7.2, 7.2)

 

2.30 qd (7.2, 7.2)

3

 

6.31 dd (15.0, 10.2)

 

6.50 dt (15.0, 7.2)

 

6.51 dt (15.0, 7.2)

4

 

5.72 dd (15.0, 7.2)

 

6.76 ddt (15.0, 12.0, 1.2)

 

6.78 ddt (15.0, 10.2, 1.2)

5

 

4.06 m

 

7.20 d (12.0)

 

7.22 d (10.2)

6

 

3.70 t (7.8)

    

7

 

2.83 quintet (7.8)

 

5.43 s

 

5.44 s

8

 

5.61 dd (14.4, 7.8)

    

9

 

6.20 dd (14.4, 10.2)

 

6.41 dd (15.6, 1.8)

 

6.38 dd (15.6, 1.2)

10

 

6.23 ddt (15.0, 10.2, 1.2)

 

6.98 ddd (15.6, 5.0, 1.8)

 

6.79 dd (15.6, 6.0)

11

 

5.76 dt (15.0, 5.4)

 

4.25 br q (5.0)

 

3.85 qd (6.0, 1.2)

12a

 

4.08 dd (5.4, 1.2)

 

3.51 dd (10.8, 5.0)

 

3.55 dd (10.2, 6.0)

12b

   

3.48 dd (10.8, 5.0)

 

3.49 dd (10.2, 6.0)

13a

 

4.06 b

 

9.42 s

 

9.42 s

13b

 

3.70 t (7.8)

    

11-OCH3

     

3.31 s

  1. aMeasured in methanol-d4 (600 MHz)
  2. bSignal without multiplicity was overlapped, and was picked up from HSQC experiment