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Efficient Stille Cross-Coupling Reaction Catalyzed by the Pd(OAc)2/Dabco Catalytic System

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The First General Method for Stille Cross-Couplings of Aryl Chlorides
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N-Heterocyclic Carbenes: A New Concept in Organometallic Catalysis
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The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]
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Homogeneous Catalysis with Metal Phosphine Complexes
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trans-Pd(OAc)2(Cy2NH)2 catalyzed Suzuki coupling reactions and its temperature-dependent activities toward aryl bromides
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Palladium complexes containing rigid bidentate nitrogen ligands as catalysts for carboncarbon bond formation
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Dabco as an Inexpensive and Highly Efficient Ligand for Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reaction

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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1,4-Diazabicyclo [2.2.2]octane
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Stille Coupling
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Formation of Alkanes and Arenes by Coupling Reactions
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Efficient Stille Cross‐Coupling Reaction Catalyzed by the Pd(OAc)2/Dabco Catalytic System.
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Introduction
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Experimental
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