Organic & Biomolecular Chemistry · 2022 · 24 citations · 88 references
Natural SciencesChemical EngineeringChemistryGreen ChemistryInorganic ChemistryReaction EngineeringInorganic SynthesisSafer Chemical SynthesisFunctional Group ToleranceRegioselective OxidationSelenium Chemistry
) as a reaction promoter under ambient conditions has been developed. The present protocol showed broad functional group tolerance and easy-to-operate and time-economical features. Additionally, this protocol also allows access to 3-seleno and 3-thiocyanoindoles by the use of readily available selenocyanate and thiocyanate salts. A mechanistic study indicated that the transformation operated through selenenyl iodide-induced electrophilic substitution processes.
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Indole synthesis – something old, something new
Martyn Inman, Christopher J. Moody · Chemical Science · 2012 · 646 citations
Chiral selenium compounds in organic synthesis
Thomas Wirth · Tetrahedron · 1999 · 295 citations
A Visible-Light-Promoted Aerobic Metal-Free C-3 Thiocyanation of Indoles
Weigang Fan, Qi Yang, Fengshan Xu et al. · The Journal of Organic Chemistry · 2014 · 219 citations