Author/Authors :
Lutz Jr.، نويسنده , , Marlon R. and Zeller، نويسنده , , Matthias and Becker، نويسنده , , Daniel P.، نويسنده ,
Abstract :
The Beckmann rearrangement has been performed on the oxime of cyclotriveratrylene (CTV) with thionyl chloride affording the ring-expanded 10-membered ring amide exclusively in high yield. Modified conditions afford a helical pentacycle derived from an unusual tandem Beckmann rearrangement and electrophilic aromatic addition followed by demethylation and tautomerization.