Review
Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids
Article first published online: 11 APR 2007
DOI: 10.1002/anie.200604335
Copyright © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Fürstner, A. and Davies, Paul W. (2007), Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids. Angew. Chem. Int. Ed., 46: 3410–3449. doi: 10.1002/anie.200604335
Publication History
- Issue published online: 27 APR 2007
- Article first published online: 11 APR 2007
- Manuscript Received: 23 OCT 2006
Funded by
- Max-Planck Society
- Fonds der Chemischen Industrie
- Abstract
- Article
- References
- Cited By
Keywords:
- alkynes;
- carbenes;
- natural products;
- noble metals;
- rearrangement
Abstract
The ability of platinum and gold catalysts to effect powerful atom-economic transformations has led to a marked increase in their utilization. The quite remarkable correlation of their catalytic behavior with the available structural data, coordination chemistry, and organometallic reactivity patterns, including relativistic effects, allows the underlying principles of catalytic carbophilic activation by π acids to be formulated. The spectrum of reactivity extends beyond their utility as catalytic and benign alternatives to conventional stoichiometric π acids. The resulting reactivity profile allows this entire field of catalysis to be rationalized, and brings together the apparently disparate electrophilic metal carbene and nonclassical carbocation explanations. The advances in coupling, cycloisomerization, and structural reorganization—from the design of new transformations to the improvement to known reactions—are highlighted in this Review. The application of platinum- and gold-catalyzed transformations in natural product synthesis is also discussed.

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