From: Anti-cancer activity of novel dibenzo[b,f]azepine tethered isoxazoline derivatives
H-H-COSY | 1H NMR | 13C NMR | ||
---|---|---|---|---|
Position | Chemical Shifts in ppm | Position | δ ppm1H | δ ppm13C |
H 4a | 3.153/3.208 | |||
3.153/4.886 | H 4ax (C-4) | 3.18 | 38.15 | |
H 4b | 3.208/3.153 | |||
3.208/4.886 | H 4eq (C-4) | 3.36 | 38.15 | |
H 6a | 3.483/4.295 | |||
3.483/4.886 | H 6a (C-6) | 3.59 | 53.7 | |
H 6b | 4.295/3.483 | |||
4.295/4.886 | H 6b (C-6) | 4.31 | 53.7 | |
H 5 | 4.886/3.153 | |||
4.886/3.208 | ||||
4.886/3.483 | ||||
4.886/4.296 | H 5 (C-5) | 4.91 | 78.7 | |
C-3 | 155.56 | |||
Ar-H | 6.5-7.7 | 120-136 |