Efficient, Transition Metal Mediated, Sequential, Two- and Three-Component Coupling Reactions for the Synthesis of Highly Substituted Five-Membered Ring Carbocycles
Autor: | Didier Bouyssi, Nicolas Coia, Geneviève Balme |
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Rok vydání: | 2007 |
Předmět: | |
Zdroj: | ChemInform. 38 |
ISSN: | 1522-2667 0931-7597 |
DOI: | 10.1002/chin.200743063 |
Popis: | A Cu-catalysed method for the preparation of highly substituted methylenecyclopentanes, through a sequence involving a Michael addition of stabilized enolates to activated enynes followed by an intramolecular carbocupration reaction, is presented. This method was also successfully combined with a Pd-mediated coupling reaction to perform a new three-component reaction through a transmetallation pathway on the vinylcopper intermediate. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) |
Databáze: | OpenAIRE |
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