Electrochemically promoted nucleophilic aromatic substitution in room temperature ionic liquids - An environmentally benign way to functionalize nitroaromatic compounds

Keyphrases

• Nucleophilic Aromatic Substitution 100%
• Nitroaromatic Compounds 100%
• Room Temperature Ionic Liquid 100%
• Environmentally Benign 100%
• Regioselectivity 40%
• 1,3,5-Trinitrobenzene 40%
• Popular 20%
• Organic Solvents 20%
• Nitroaromatics 20%
• Amines 20%
• Hydrides 20%
• Atom Economy 20%
• Ketones 20%
• Nucleophile 20%
• Alternative Solvents 20%
• Economic Cost 20%
• Electrochemical Approach 20%
• Electrocatalysis 20%
• Green Synthetic Route 20%
• Electrochemical Studies 20%
• Cyanide 20%
• Solvation Effect 20%
• 1-Ethyl-3-methylimidazolium Acetate 20%
• Nitrotoluene 20%
• Electrosynthesis 20%
• Supporting Electrolyte 20%
• Ionic Liquid Solvents 20%
• 1-chloro-2 20%
• 1-Butyl-3-methylimidazolium Bis(trifluoromethylsulfonyl)imide 20%
• Nucleophilic Aromatic Substitution Reaction 20%
• Trinitrobenzene 20%
• Aprotic Solvent 20%
• Methoxide 20%
• Nitroarenes 20%
• Dinitroaniline 20%
• Electrolyte Systems 20%
• Green Alternatives 20%
• 1-Butyl-3-methylimidazolium Tetrafluoroborate 20%
• 1-Butyl-3-methylimidazolium Hexafluorophosphate 20%
• Dinitronaphthalene 20%
• Electrocatalyses 20%

Chemistry

• Nucleophilic Aromatic Substitution 100%
• Ambient Reaction Temperature 100%
• Ionic Liquid 100%
• 1-Butyl-3-Methylimidazolium 60%
• Regioselectivity 40%
• Ketones 20%
• Solvation 20%
• Electrocatalysis 20%
• 4-Nitrotoluene 20%
• BF 4 20%
• 1,3-dinitronaphthalene 20%
• 1,3-dinitrobenzene 20%
• 2,4-dinitroaniline 20%
• 1,3,5-trinitrobenzene 20%
• Methoxide 20%
• 1-chloro-2,4,6-trinitrobenzene 20%
• Aprotic Solvent 20%
• Supporting Electrolyte 20%
• Nitroarene 20%
• Nucleophile 20%
• Imide 20%
• 1-Butyl-3-Methylimidazolium Tetrafluoroborate 20%