Publication | Closed Access
Monofluorovinyl Tosylate: A Useful Building Block for the Synthesis of Terminal Vinyl Monofluorides via Suzuki−Miyaura Coupling
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Citations
35
References
2010
Year
Arylboronic AcidsTerminal Vinyl MonofluoridesCross-coupling ReactionEngineeringAlkene MetathesisMonofluorovinyl TosylatePractical Vinyl FluorideFluorous SynthesisOrganic ChemistrySuzuki−miyaura CouplingCatalysisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective Synthesis
Monofluorovinyl tosylate was developed as a practical vinyl fluoride building block to couple with a variety of arylboronic acids in the presence of a palladium catalyst. The high stereoselectivity of 2-aryl-1-fluoroethene derivatives was achieved. This approach is also applicable to the synthesis of 2,2-diaryl-1-fluoroethenes in good yields.
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