Organic Letters · 2014 · 77 citations · 48 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryMolecular PharmacologySynthetic Medicinal ChemistryCross-coupling ReactionsRetrosynthetic AnalysisIndole ChemistryIndole DerivativesIndole SynthesisMedicinal Chemistry ApplicationsOxidative CouplingOxidative Coupling ReactionsOxidative Cross-couplingSubstrate Scope
The first C3-dicarbonylation of indoles was realized through direct oxidative cross-coupling of indoles with methyl ketones in the presence of molecular iodine and pyrrolidine. This reaction constructed a highly efficient indolyl diketones scaffold, which might be regarded as a useful biological and pharmacological tool in the exploration of therapeutic A2BAR modulators. The use of inexpensive molecular iodine and pyrrolidine and a broad substrate scope make this protocol very practical. Preliminary mechanistic studies indicate that two paths are involved in this process.
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Chao Liu, Hua Zhang, Wei Shi et al. · Chemical Reviews · 2011 · 1.8K citations
Synthetic Use of Molecular Iodine for Organic Synthesis
Hideo Togo, Shinpei Iida · Synlett · 2006 · 412 citations