Convergent total synthesis of lamellarin K

Martin Banwell, Bernard Flynn, David Hockless

Research output: Contribution to journalArticleResearchpeer-review

104 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)2259-2260
Number of pages2
JournalChemical Communications
Issue number23
Publication statusPublished - 1 Jan 1997
Externally publishedYes

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