Publication | Closed Access
Development of a Novel, Highly Efficient Halide-Catalyzed Sulfenylation of Indoles
191
Citations
10
References
2006
Year
Chemical EngineeringNovel OrganocatalystsEngineeringOrganic ChemistryCatalysisSulfenylated IndolesChemistryHalide-containing SaltsStereoselective SynthesisNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringEfficient Reaction
[reaction: see text] The reaction of a variety of indoles with N-thioalkyl- and N-thioarylphthalimides to produce 3-thioindoles is reported. Catalytic quantities of halide-containing salts are crucial to the success of this reaction. This highly efficient reaction provides sulfenylated indoles from bench-stable, readily available starting materials in good to excellent yields.
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