Nitrogen-, phosphorus-, and sulfur-containing palladacycles, typically containing four- or six-electron donor anionic metallated ligands, are emerging as a new family of organometallic catalyst precursors. These thermally and air-stable complexes are easy to handle and their synthesis is often straightforward. Palladacycles are now being successfully exploited in catalytic reactions ranging from classical hydrogenations to enantioselective aldol-type condensations. The main recent achievements pertaining to their use in homogeneous organometallic catalysis are outlined herein.
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Dupont et al. (2001) studied this question.
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