B. Gigante et al., C-13 AND H-1-NMR ASSIGNMENTS FOR A SERIES OF DEHYDROABIETIC ACID-DERIVATIVES, Magnetic resonance in chemistry, 33(4), 1995, pp. 318-321
Reliable assignments were made for a series of nitro and amine C ring-
substituted dehydroabietic acid derivatives, the main resin acid prese
nt in disproportionated rosin and an important intermediate in the che
mical industry. A combination of 1D and 2D NMR techniques, including H
ETCORR, COSY and DEFT experiments, was used. Quaternary carbon atoms,
mainly aromatic substituted, require care owing to assignment difficul
ties that are based on calculated data and are confirmed by long-range
H-1, C-13 NMR correlation with selective INEPT and the proton-detecte
d HMBC experiment.