Issue 17, 2009

Palladium-catalysed synthesis of 1-isoindolecarboxylic acidesters and sequential Diels–Alder reactions: access to bridged- and fused-ring heterocycles

Abstract

The Pd-catalysed intramolecular α-arylation of α-amino acid esters provides a useful methodology for the synthesis of substituted isoindole derivatives, which have been used in Diels–Alder reactions to access diverse skeletal frameworks.

Graphical abstract: Palladium-catalysed synthesis of 1-isoindolecarboxylic acid esters and sequential Diels–Alder reactions: access to bridged- and fused-ring heterocycles

Supplementary files

Article information

Article type
Communication
Submitted
18 May 2009
Accepted
02 Jul 2009
First published
09 Jul 2009

Org. Biomol. Chem., 2009,7, 3382-3384

Palladium-catalysed synthesis of 1-isoindolecarboxylic acid esters and sequential Diels–Alder reactions: access to bridged- and fused-ring heterocycles

D. Solé and O. Serrano, Org. Biomol. Chem., 2009, 7, 3382 DOI: 10.1039/B909701E

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