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Pd-Catalyzed Copper-Free Carbonylative Sonogashira Reaction of Aryl Iodides with Alkynes for the Synthesis of Alkynyl Ketones and Flavones by Using Water as a Solvent
192
Citations
48
References
2005
Year
Room TemperatureChemical EngineeringCross-coupling ReactionEngineeringAryl IodidesCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryBalloon PressureAsymmetric CatalysisAlkynyl Ketones
The Pd-catalyzed copper-free carbonylative Sonogashira coupling reaction to synthesize alkynyl ketones from terminal alkynes and aryl iodides was achieved by using water as a solvent. The reaction was carried out at room temperature under balloon pressure of CO with Et(3)N as a base. The developed method was successfully applied to the synthesis of flavones.
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