Issue 23, 1997

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.

Article information

Article type
Paper

Chem. Commun., 1997, 2259-2260

Convergent total synthesis of lamellarin K†

M. Banwell and D. Hockless, Chem. Commun., 1997, 2259 DOI: 10.1039/A705874H

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