Publication | Closed Access
Pd-Catalyzed Cross-Coupling Reaction of Alkyl Tosylates and Bromides with Grignard Reagents in the Presence of 1,3-Butadiene
86
Citations
13
References
2003
Year
Asymmetric CatalysisRoom TemperatureChemical EngineeringCross-coupling ReactionEngineeringAlkene MetathesisGrignard ReagentsOrganic ChemistryOrganometallic CatalysisCatalysisChemistryPd-catalyzed Cross-coupling ReactionEnantioselective SynthesisAlkyl Tosylates
Abstract A new method for cross-coupling reaction of alkyl tosylates and bromides with Grignard reagents has been developed by the use of Pd(acac)2 or PdCl2 as the catalyst. Addition of 1,3-butadiene is essential to afford good yields of coupling products. This reaction proceeds efficiently at room temperature using primary and secondary alkyl and aryl Grignard reagents.
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