European Journal of Organic Chemistry · 2018 · 14 citations · 47 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst CharacterizationCatalytic MechanismsHeterogeneous CatalysisMetal CatalysisOrganic SynthesisSupported CatalystsAlkylation CatalysisAlkylation ProcessesAlkylation ReactionsCatalytic Reaction MechanismsHeteroaromatic CompoundsPincer ComplexesTransition Metal-catalyzed SynthesisTransition-metal-catalyzed Functionalization
Hydrogen‐autotransfer alkylation (HAT or “borrowing‐hydrogen” alkylation) of heteroaromatic compounds has been studied with a range of substrates recently, but pyrroles have been largely absent from such studies. The conditions for HAT alkylations of pyrroles were investigated under a variety of conditions and were found to take place under basic alcoholic conditions (Hans Fischer alkylation) in the absence of transition‐metal catalysts; by means of a heterogeneous Pd/C catalyst in the presence of base; and finally by means of homogeneous transition‐metal catalysis combining a base and iridium pincer complexes generated in situ that have not previously been used in HAT alkylations of heterocycles.
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The Catalytic Amination of Alcohols
Sebastian Bähn, Sebastian Imm, Lorenz Neubert et al. · ChemCatChem · 2011 · 739 citations
A sustainable catalytic pyrrole synthesis
Stefan Michlik, Rhett Kempe · Nature Chemistry · 2013 · 486 citations