Palladium-Catalyzed Direct Ortho Aroylation of 2‑Phenoxypyridines with Aldehydes and Catalytic Mechanism Investigation

Abstract

A direct ortho aroylation of 2-phenoxypyridines with aldehydes leading to aryl ketones by the use of palladium­(II) acetate, <i>tert</i>-butyl hydroperoxide, and chlorobenzene as the catalyst, oxidant, and solvent, respectively, is presented. Intra- and intermolecular kinetic isotope effects, radical trapping, and controlled experiments were carried out to support the proposed catalytic mechanism for the reaction. Syntheses of (2-hydroxyphenyl)­(phenyl)­methanones and 1-hydroxy-9<i>H</i>-fluoren-9-ones directed from ortho-aroylated 2-phenoxypyridines were demonstrated

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Last time updated on 12/02/2018

This paper was published in FigShare.

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