Organic Letters · 2021 · 23 citations · 34 references
Natural SciencesChemistryGreen ChemistryOrganic ChemistryPolymer ChemistryCross-coupling ReactionsGreen Polymer ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisSafer Chemical SynthesisCross-coupling CatalysisGreen Heterocycle SynthesisHeterocycle FunctionalizationNickel-catalyzed Cross-couplingReductive Cross-couplingSilane Coupling
A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.
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Updating and further expanding GSK's solvent sustainability guide
Catherine M. Alder, John Hayler, Richard K. Henderson et al. · Green Chemistry · 2016 · 1K citations
Reductive Cross‐Coupling Reactions between Two Electrophiles
Christiane E. I. Knappke, Sabine Grupe, Dominik Gärtner et al. · Chemistry - A European Journal · 2014 · 750 citations · Full text