Impacts of Steric Compression, Protonation, and Intramolecular Hydrogen Bonding on the N NMR Spectroscopy of Norditerpenoid Alkaloids and Their Piperidine-Ring Analogues

H-N HMBC spectra of norditerpenoid alkaloids and their synthetic azabicyclic analogues were obtained to investigate the impacts of the through-space effect of steric compression, protonation, and formation of intramolecular hydrogen bonding on the N NMR spectroscopy of these natural products and their piperidine-containing analogues. A rare N NMR effect of steric compression is demonstrated in half-cage A/E-rings of norditerpenoid alkaloid free bases and their synthetic azabicyclic analogues, in which the distribution of the lone pair of electrons of the tertiary amine -atom is sterically restricted by bridged cycloalkanes, e.g., cyclopentane, cyclohexane, and cycloheptane rings. This results in significant changes in the N chemical shift, typically by at least ∼10 ppm. The lone pair of electrons of the -atom in the piperidine ring are sterically compressed whether the bridged cyclohexane ring adopts a chair or boat conformation. The N chemical shifts of 1α-OMe norditerpenoid alkaloid free bases significantly increase (Δδ ≥ 15.6 ppm) on alkaloid protonation and thence the formation of an intramolecular hydrogen bond between -H and 1α-OMe. The intramolecular hydrogen bonds between the -atom and 1α-OH of 1α-OH norditerpenoid alkaloid free bases, karacoline, condelphine, and neoline stabilize their A-rings, adopting an unusual twisted-boat conformation, and they also significantly increase δ of the tertiary amine -atom.