The Journal of Organic Chemistry · 2020 · 47 citations · 76 references
Cross-coupling ReactionEngineeringPropargyl ElectrophilesAlkene MetathesisPropargyl ElectrophilePalladium-propargyl IntermediateElectrosynthesisOrganometallic CatalysisCatalysisChemistryPalladium CatalysisBiomolecular Engineering
The propargyl electrophile has proven to be a versatile reactant when coupled with palladium catalysis. Its versatility is owed to the several reaction pathways that the palladium-propargyl intermediate can proceed by, and the outcome can be predictably controlled by varying several factors. The tunable nature of the propargyl electrophile along with its versatility are detailed herein. The initial reports for each of the pathways are highlighted along with a discussion of more recent developments in the field.
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Tetsuo Tsuda, Yoshiki Chujo, Seiichi Nishi et al. · Journal of the American Chemical Society · 1980 · 225 citations
Palladium-Catalyzed Cyclization of Propargylic Compounds
Li‐Na Guo, Xin‐Hua Duan, Yong‐Min Liang · Accounts of Chemical Research · 2010 · 212 citations · Full text
Douglas C. Behenna, Justin T. Mohr, Nathaniel H. Sherden et al. · Chemistry - A European Journal · 2011 · 201 citations
Prochiral Enolate, α-Quaternary Ketones, Mechanistic Studies +11