Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5217367 | Tetrahedron | 2013 | 8 Pages |
Abstract
Novel developments are described, which have been achieved in the framework of the studies of sequential palladium-catalyzed reactions, involving palladacycle formation with norbornene or norbornadiene via aromatic C–H activation. The use of o-bromophenols as partners of iodobenzenes has led to ring formation after norbornene deinsertion, or to arylphenols, containing a pendant norbornenyl or norbornadienyl group or to vinylarylphenols. The availability of a reductive elimination step drives the reaction course toward a preferential product.
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