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Issue 4, 2013
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A mild entry to isoindolinones from furfural as renewable resource

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Abstract

A convenient transformation of furfural and derivatives into arene compounds is described. This process provides a straightforward access to isoindolinones from a renewable resource via the sequence of a tandem Ugi–Diels–Alder process followed by a ring-opening, dehydrating aromatisation. Five bonds are created and water is the sole by-product during this two-step sequence.

Graphical abstract: A mild entry to isoindolinones from furfural as renewable resource

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Publication details

The article was received on 19 Nov 2012, accepted on 23 Jan 2013 and first published on 24 Jan 2013


Article type: Paper
DOI: 10.1039/C3NJ41050A
Citation: New J. Chem., 2013,37, 1195-1200
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    A mild entry to isoindolinones from furfural as renewable resource

    G. Caillot, S. Hegde and E. Gras, New J. Chem., 2013, 37, 1195
    DOI: 10.1039/C3NJ41050A

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