Efficient, Transition Metal Mediated, Sequential, Two- and Three-Component Coupling Reactions for...
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Transcript of Efficient, Transition Metal Mediated, Sequential, Two- and Three-Component Coupling Reactions for...
2007
Cyclopentane derivativesQ 0030 Efficient, Transition Metal Mediated, Sequential, Two- and Three-Component
Coupling Reactions for the Synthesis of Highly Substituted Five-Membered Ring Carbocycles. — An efficient method for the synthesis of methylenecyclopentanes, e.g. (III), (V) and (VIII), is presented, involving a Michael addition of a stabilized enolate with an activated enyne followed by intramolecular carbocupration. Combination of this method with palladium-catalyzed arylation then affords the corresponding aryl-methylene analogues (XIV) in a one-pot reaction. — (COIA, N.; BOUYSSI, D.; BALME*, G.; Eur. J. Org. Chem. 2007, 19, 3158-3165; Inst. Chim. Biochim. Mol. Supramol., CNRS, Univ. Lyon 1, F-69622 Lyon, Fr.; Eng.) — Mischke
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