Nitrogenous Educts through Oxidative
Amidation of Phenols:  The Bimolecular
Reaction

Canesi, Sylvain; Bouchu, Denis; Ciufolini, Marco A.

doi:10.1021/ol048094v.s001

ol048094v_si_001.pdf (240.72 kB)

Nitrogenous Educts through Oxidative Amidation of Phenols: The Bimolecular Reaction

journal contribution

posted on 2005-01-20, 00:00 authored by Sylvain Canesi, Denis Bouchu, Marco A. Ciufolini

The elusive oxidative amidation of phenols to 4-aza-substituted dienones in the bimolecular mode may be achieved by treatment with iodobenzene diacetate (“DIB”) in a mixture of hexafluoro-2-propanol and acetonitrile.

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Keywords

hexafluoro DIB diacetate Phenol Oxidative Amidation phenol mixture Nitrogenous Educts iodobenzene oxidative amidation acetonitrile mode dienone Bimolecular Reaction

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