Abstract
The synthesis of 4-aryl-1,2,3,4-tetrahydroisoquinolines is achieved via the ether rearrangement methodology. Subsequent reactions yielded cherylline and ether derivatives of amaryllidaceac alkaloids.
GRAPHICAL ABSTRACT
![](/cms/asset/3c3924b5-9ff8-448a-9d12-143618f521cd/lsyc_a_891745_o_uf0001.gif)
ACKNOWLEDGMENT
We thank Suven Life Sciences for the excellent analytical facilities and allowing us to publish these results.