Chemical Communications · 2019 · 24 citations · 39 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisSulfur ChemistrySulfur CompoundsBenzimidazole ChemistryBenzimidazole SynthesisBenzothiazole SynthesisBenzoxazole SynthesisElemental Sulfur ChemistryElemental Sulfur OxidationOne-pot Heterocycle SynthesisThiazole Chemistry
A novel and direct strategy has been developed for the synthesis of 2-(2,2,2-trifluoroethyl)benzoxazoles by reaction of o-aminophenols and 2-bromo-3,3,3-trifluoropropene in the presence of elemental sulfur under metal-free conditions. The scope of this methodology was further extended to the synthesis of the trifluoroethylated benzothiazole and benzoimidazole derivatives. A plausible mechanism was proposed on the basis of isolation and characterization of a thioamide intermediate.
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Practical and innate carbon–hydrogen functionalization of heterocycles
Yuta Fujiwara, Janice A. Dixon, Fionn O’Hara et al. · Nature · 2012 · 924 citations · Full text