Issue 12, 2011

Intramolecular palladium-catalysed enolate arylation of 2- and 3-iodoindole derivatives for the synthesis of β-carbolines, γ-carbolines, and pyrrolo[3,4-b]indoles

Abstract

The palladium-catalysed intramolecular α-arylation of carbonyl compounds with amino-tethered 2- and 3-iodoindoles provides a useful methodology for the synthesis of indolo-b-fused nitrogen heterocycles. A variety of substituted tetrahydro β- and γ-carbolines, and pyrrolo[3,4-b]indoles, have been prepared by means of this palladium-catalysed annulation process.

Graphical abstract: Intramolecular palladium-catalysed enolate arylation of 2- and 3-iodoindole derivatives for the synthesis of β-carbolines, γ-carbolines, and pyrrolo[3,4-b]indoles

Supplementary files

Article information

Article type
Paper
Submitted
17 Jan 2011
Accepted
25 Mar 2011
First published
25 Mar 2011

Org. Biomol. Chem., 2011,9, 4535-4544

Intramolecular palladium-catalysed enolate arylation of 2- and 3-iodoindole derivatives for the synthesis of β-carbolines, γ-carbolines, and pyrrolo[3,4-b]indoles

D. Solé, M.-Lluïsa Bennasar and I. Jiménez, Org. Biomol. Chem., 2011, 9, 4535 DOI: 10.1039/C1OB05087G

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