The Journal of Organic Chemistry · 2016 · 40 citations · 73 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCatalyst DesignCatalyst PreparationHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisFuran ChemistryFuran SynthesisFuransIndole ChemistryIndole SynthesisOne-pot Library SynthesisSonogashira CouplingSuzuki - Miyaura Coupling
Disubstituted benzo[b]furans were synthesized by ortho-selective Sonogashira coupling of dichlorophenols and terminal alkynes, followed by cyclization and Suzuki-Miyaura coupling in one pot, using a palladium-dihydroxyterphenylphosphine (Cy-DHTP) catalyst. The use of substoichiometric amounts of tetrabutylammonium chloride was effective in accelerating the Suzuki-Miyaura coupling. This protocol was also successfully applied to the one-pot synthesis of disubstituted indoles from dichloroaniline derivatives.
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Xiaohua Huang, Kevin W. Anderson, Danilo Zim et al. · Journal of the American Chemical Society · 2003 · 767 citations
Indole synthesis – something old, something new
Martyn Inman, Christopher J. Moody · Chemical Science · 2012 · 646 citations