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Highly Selective Palladium-Catalyzed Cross-Coupling of Secondary Alkylzinc Reagents with Heteroaryl Halides

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Highly_Selective_Palladium_Catalyzed_Cross_Coupling_of_Secondary_Alkylzinc_Reagents_with_Heteroaryl_Halides/2038890
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The highly selective palladium-catalyzed Negishi coupling of secondary alkylzinc reagents with heteroaryl halides is described. The development of a series of biarylphosphine ligands has led to the identification of an improved catalyst for the coupling of electron-deficient heterocyclic substrates. Preparation and characterization of oxidative addition complex (L)­(Ar)­PdBr provided insight into the unique reactivity of catalysts based on CPhos-type ligands in facilitating challenging reductive elimination processes.
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2015-12-17
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