Convergent total synthesis of lamellarin K†
Abstract
The azomethine ylide derived from dihydroisoquinolinium salt 24 undergoes an intramolecular [3 + 2] cycloaddition reaction to give pyrrole 25 which upon de-isopropylation affords the marine alkaloid lamellarin K 4.
- This article is part of the themed collection: RACI100: Celebrating Australian Chemistry