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Journal of the American Chemical Society 2019-Jun

Enantioselective Total Synthesis of (+)-Dihydro-β-erythroidine.

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Sebastian Clementson
Mikkel Jessing
Henrik Pedersen
Paulo Vital
Jesper Kristensen

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Abstrè

Erythrina alkaloids represent a rich source of complex polycyclic, bioactive natural products. In addition to their sedative and hypotensive effect, their curare-like activity and structural framework have made them attractive targets for synthetic and medicinal chemists. (+)-Dihydro-β-erythroidine (DHβE), the most potent nicotine acetylcholine receptor antagonist (nAChR) of the Erythrina family, is synthesized for the first time in 13 steps from commercially available material.

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