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An exceptional palladium-catalyzed alkenylation of silyl enol ether in the absence of a fluoride additive
Authors:Hiroki Shigehisa
Affiliation:Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo 142-8501, Japan
Abstract:An exceptional intramolecular palladium-catalyzed alkenylation of silyl enol ether in the absence of a fluoride additive was developed, and this reaction led to the construction of bicyclo[3.3.1]nonane ring system in reasonable yield. In this type of reactions, trialkylamines were employed as additives instead of previously indispensable fluoride additives.
Keywords:Palladium-catalyzed alkenylation   Intramolecular C-C bond formation   Silyl enol ether   Bicyclo[3.3.1]nonane   Trialkylamine
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