FeCl3-mediated Friedel-Crafts hydroarylation with electrophilic N-acetyl indoles for the synthesis of benzofuroindolines.
Rodolphe Beaud, Régis Guillot, Cyrille Kouklovsky, Guillaume Vincent
Index: Angew. Chem. Int. Ed. Engl. 51(50) , 12546-50, (2012)
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Abstract
IRONic electrophilic indoles! The C3-regioselective hydroarylation of N-acetyl indoles with aromatic nucleophiles mediated by FeCl(3) features a rare example of the electrophilic reactivity of the indole core in a Friedel-Crafts reaction. This indole umpolung allows us straightforward access to the tetracyclic benzofuroindoline motif found in the natural product diazonamide A, which is a potent antitumor agent.Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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