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Issue 13, 1994
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A new route to the isoindole nucleus via Furan–pyrrole ring-exchange

Abstract

Isoindole is readily synthesized via intramolecular cycloaddition and sucessive ring opening of Boc-protected furfuryl propargylamine in the presence of base.

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Article type: Paper
DOI: 10.1039/C39940001535
Citation: J. Chem. Soc., Chem. Commun., 1994,0, 1535-1535

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    A new route to the isoindole nucleus via Furan–pyrrole ring-exchange

    M. Lee, H. Moritomo and K. Kanematsu, J. Chem. Soc., Chem. Commun., 1994, 0, 1535
    DOI: 10.1039/C39940001535

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