Publication | Closed Access
α-Allenyl Ethers as Starting Materials for Palladium Catalyzed Suzuki–Miyaura Couplings of Allenylphosphine Oxides with Arylboronic Acids
41
Citations
70
References
2014
Year
Arylboronic AcidsChemical EngineeringCross-coupling ReactionAryl EthersEngineeringAlkene Metathesisα-Allenyl EthersNatural SciencesDiversity-oriented SynthesisOrganic ChemistryAllenylphosphine OxidesOrganometallic CatalysisCatalysisChemistryCatalytic Synthesis
We disclose here the first palladium-catalyzed Suzuki-Miyaura couplings of aryl ethers functionalized allenylphosphine oxides with arylboronic acids. This new methodology with α-allenyl ethers as starting materials provides a novel approach to generate phosphinoyl 1,3-butadienes and derivatives with medium to excellent yields. The reaction tolerates a variety of functional groups to afford ranges of structurally diverse substituted phosphionyl 1,3-butadienes. For unsymmetrical allene substrates, high stereospecific additions to give E-isomers are usually observed. On the basis of the known palladium and allene chemistry, a mechanism is proposed.
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