Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.

Issue 23, 1997
Previous Article Next Article

Convergent total synthesis of lamellarin K†


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.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A705874H
Chem. Commun., 1997, 2259-2260

  •   Request permissions

    Convergent total synthesis of lamellarin K†

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

Search articles by author