2005
DOI: 10.1016/j.jfluchem.2004.11.003
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Highly selective electrochemical fluorination of organic compounds in ionic liquids

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Cited by 51 publications
(30 citation statements)
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References 24 publications
(22 reference statements)
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“…These studies indicate high selectivity toward fluorination of active methylene group attached to sulfur atom [5][6][7][8].…”
Section: Introductionmentioning
confidence: 77%
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“…These studies indicate high selectivity toward fluorination of active methylene group attached to sulfur atom [5][6][7][8].…”
Section: Introductionmentioning
confidence: 77%
“…Partial fluorination of aromatic compounds by electrochemical method in fluoride containing solvent-free electrolyte systems has been extensively studied and reviewed [5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…Chemical fluorination can also be achieved by using halide exchange process [19] or by employing other novel fluorinating agents [20]. Solvent free Et 3 N Á nHF and Et 4 NF Á mHF has been successfully employed for anodic fluorination of compounds which are more difficult to fluorinate in presence of solvents [21,23,[25][26][27][28][29].…”
Section: Introductionmentioning
confidence: 99%
“…ILs have made significant progress in recent years in the catalytic processes. [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30] They are liquid salts in which the ions are poorly coordinated. ILs are not simply salts dissolved in liquid but they usually exist as liquid below 100 °C, or even at room temperature (room temperature ionic liquids; RTILs).…”
Section: Introductionmentioning
confidence: 99%