Publication | Closed Access
Electro‐Oxidative Coupling of Azoles with 2‐ and 3‐Haloindoles/Thiophenes Providing Access to 2/3‐Halo(Azol‐1‐Yl)Indoles/Thiophenes
15
Citations
42
References
2021
Year
Organic Material ChemistryChemical EngineeringCross-coupling ReactionEngineeringOrganic ElectrochemistryNatural SciencesDiversity-oriented SynthesisOrganometallic ElectrochemistryOrganic ChemistryElectrochemical ApproachOrganometallic CatalysisCatalysisElectro‐oxidative CouplingChemistryHeterocycle ChemistryHydrogen GasFunctional Indoles
Abstract This report discloses an electrochemical oxidative C−H/N−H cross coupling method for the synthesis of C‐2/C‐3 azolated halo‐indoles/thiophenes under metal catalyst‐free and external chemical oxidant free condition. Hydrogen gas was the only byproduct of this C−H/N−H cross‐coupling reaction. The synthetic utility of this electrochemical approach is highlighted by its easy scalabity and compatibility with highly functional indoles and azoles. The retention of halogen on the heterocycles could serve as a useful functional group for future late‐stage modifications. magnified image
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