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N‐Heterocyclic Carbene Derived Nickel–Pincer Complexes: Efficient and Applicable Catalysts for Suzuki–Miyaura Coupling Reactions of Aryl/Alkenyl Tosylates and Mesylates
142
Citations
81
References
2009
Year
Inorganic ChemistryChemical EngineeringCross-coupling ReactionEngineeringAryl/alkenyl TosylatesNhc‐derived Nickel–pincer ComplexesNatural SciencesNickelacycle 1ADiversity-oriented SynthesisCatalytic SynthesisSuzuki–miyaura Coupling ReactionsAlkenylboronic AcidsApplicable CatalystsOrganometallic CatalysisCatalysisMolecular CatalysisChemistryBiomolecular Engineering
Abstract Catalytic activities of NHC‐derived nickel–pincer complexes for the Suzuki–Miyaura coupling reactions of aryl/alkenyl tosylates and mesylates are described. In the presence of a catalytic amount of nickelacycle 1a , a wide array of tosylates and mesylates reacted with several aryl‐ and alkenylboronic acids to afford the coupling products, generally in high yields. Fine tuning of the reaction conditions for each class of electrophiles was achieved only by choosing the appropriate reaction medium (DME for tosylates, dioxane for mesylates).(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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