Organic Letters · 2013 · 26 citations · 21 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisIndole ChemistryIndole DerivativesIndole SynthesisOxidative DesulfurizationRing-forming ReactionsTransition Metal-catalyzed Synthesis
The cycloannulation of β-oxodithioesters and tryptamine in dichloromethane in the presence of a catalytic amount of InCl3 and TFA gave the novel 5-aryl/heteroaryl 2a(1),9b-dihydro-1H-2a,5a-diaza-cyclopenta[jk]fluorene-3(2H)-thiones in moderate to good yields. The reaction was proposed to involve a tandem transformation of thioamide, protonation, and dehydrative cyclization. KMnO4-oxidation of these newly prepared compounds yielded oxidative desulfurization products in good yields.
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Total Synthesis of (±)-Communesin F
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Structure of the Bacillus subtilis quorum-sensing peptide pheromone ComX
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Alkaloids from the Root of <i>Isatis indigotica</i>
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