The cyclization of 2-alkynylanilines in the presence of PdCl2 and nBu4NCl under an acidic CH2Cl2-HCI two-phase system affords 2-substituted indoles in good to high yield, at room temperature. The reaction is particularly suited to the one-flask preparation of 2-substituted indoles from 2-ethynylaniline.

Palladium-catalysed cyclization of 2-alkynylanilines to 2-substituted indoles under an acidic two-phase system

CARNICELLI, VERONICA;MARINELLI, Fabio
1994-01-01

Abstract

The cyclization of 2-alkynylanilines in the presence of PdCl2 and nBu4NCl under an acidic CH2Cl2-HCI two-phase system affords 2-substituted indoles in good to high yield, at room temperature. The reaction is particularly suited to the one-flask preparation of 2-substituted indoles from 2-ethynylaniline.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/11966
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