Enantioselective Total Synthesis of (+)-Dihydro-β-erythroidine
作者:Sebastian Clementson、Mikkel Jessing、Henrik Pedersen、Paulo Vital、Jesper L. Kristensen
DOI:10.1021/jacs.9b04626
日期:2019.6.5
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-beta-erythroidine (DH beta E), 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.