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Issue 23, 1997
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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.

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Article type: Paper
DOI: 10.1039/A705874H
Citation: Chem. Commun., 1997,0, 2259-2260
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    Convergent total synthesis of lamellarin K†

    M. Banwell and D. Hockless, Chem. Commun., 1997, 0, 2259
    DOI: 10.1039/A705874H

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