Hidden Heptacyclic Chiral N-Acyl Iminium Ions: A New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid-Promoted Intramolecular Pictet-Spengler Reaction.
Yasmin ReviriotBastien MicheletRodolphe BeaudAgnès Martin-MingotFrédéric GueganSébastien ThibaudeauJean RodriguezDamien BonnePublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2022)
Enantioenriched complex fused-tricyclic azepanes or bridged-polycyclic azocanes were constructed via a two-step sequence involving an enantioselective organocascade followed by superacid activation of the domino adduct. The activated oxa-bridged azepane acts as a key hidden heptacyclic chiral N-acyl iminium ion triggering a chemo- and diastereoselective intramolecular mono- or di-arylation.