2010
DOI: 10.1016/j.jfluchem.2009.11.009
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Synthesis of fluorofurans and perfluoroalkylfurans

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Cited by 20 publications
(8 citation statements)
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References 176 publications
(188 reference statements)
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“…Being interested in the synthesis of organofluorine compounds, we recently presented a detailed overview of methods for the synthesis and applications of α,β-unsaturated trifluoromethyl ketones, 13 trifluoromethyl pyrroles and trifluoromethyl indoles, 14 fluorofurans and perfluoroalkylfurans, 15 and fluorinated thiophenes and their benzo analogues. 16 Herein, we highlight methods for the synthesis of fluoropyrroles, fluoroindoles, and some other condensed anologues of fluoropyrroles ( Figure 2).…”
Section: Figurementioning
confidence: 99%
“…Being interested in the synthesis of organofluorine compounds, we recently presented a detailed overview of methods for the synthesis and applications of α,β-unsaturated trifluoromethyl ketones, 13 trifluoromethyl pyrroles and trifluoromethyl indoles, 14 fluorofurans and perfluoroalkylfurans, 15 and fluorinated thiophenes and their benzo analogues. 16 Herein, we highlight methods for the synthesis of fluoropyrroles, fluoroindoles, and some other condensed anologues of fluoropyrroles ( Figure 2).…”
Section: Figurementioning
confidence: 99%
“…Both overview of methods for the synthesis of fluorofurans and perfluoroalkylfurans [21]. More general reviews on the preparation of polyfluorinated heterocyclic and heteroaromatic compounds have been compiled by both Brooke and Yakobson [22,23].…”
Section: Conclusion 58 Introductionmentioning
confidence: 99%
“…Indeed, fluorofuran or (perfluoroalkyl)furan fragments have already been embedded within structures possessing important pharmacological properties. [9] Recently, we have reported gold-catalyzed cycloisomerization of 2-fluoroalk-3-yn-1-ones as a tool for the synthesis of unsymmetrically 2,5-disubstituted 3-fluoro-the synthesis of 2,5-disubstituted 3-bromo-4-fluoro-and 3-fluoro-4-iodofurans. The sequential procedure starts at monofluorination of the alk-1-en-3-yn-1-yl silyl ethers with Selectfluor and proceeds with good overall yields (62-78 %).…”
Section: Introductionmentioning
confidence: 99%