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Palladium-Catalyzed Oxidative Sulfenylation of Indoles and Related Electron-Rich Heteroarenes with Aryl Boronic Acids and Elemental Sulfur
108
Citations
60
References
2016
Year
Chemical EngineeringCross-coupling ReactionEngineeringAryl Boronic AcidsPalladium-catalyzed Oxidative SulfenylationSynthetic ProtocolOrganic ChemistryOrganometallic CatalysisCatalysisElemental SulfurChemistryHeterocycle ChemistrySynthetic Chemistry
An efficient and convenient palladium-catalyzed C-H bond oxidative sulfenylation of indoles and related electron-rich heteroarenes with aryl boronic acids and elemental sulfur has been described. This procedure provides a useful and direct approach for the assembly of a wide range of structurally diverse 3-sulfenylheteroarenes with moderate to excellent yields from simple and readily available starting materials. Moreover, this synthetic protocol is suitable for N-protected and unprotected indoles. Notably, the construction of two C-S bonds in one step was also achieved in this transformation.
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