Generation of arylnitrenium ions by nitro-reduction and gas-phase synthesis of N-heterocycles

Keyphrases

• Nitroarene Reduction 100%
• Arylnitrenium Ions 100%
• Gas-phase Synthesis 100%
• N-heterocycles 100%
• 1,2-dichloroethane 75%
• Ion-molecule Reactions 50%
• Chemical Ionization 50%
• Nitrobenzene 50%
• Radical Cation 50%
• Nitroaromatics 50%
• Reagent Ion 25%
• Formation Reaction 25%
• Mass Spectrometry 25%
• Chemical Reactivity 25%
• Methyl 25%
• Condensed Phase 25%
• Reduction Reaction 25%
• Oncogenesis 25%
• Phenyl 25%
• Sulfone 25%
• Explosive Detection 25%
• 1,3-dioxolane 25%
• Ortho 25%
• Indole 25%
• Regioselectivity 25%
• Vinyl Halides 25%
• Selective Method 25%
• Collision-induced Dissociation 25%
• Ethyl Vinyl Ether 25%
• Atmospheric Pressure Chemical Ionization 25%
• Direct Formation 25%
• Phase Chemistry 25%
• Reactions with nucleophiles 25%
• Benzomorpholine 25%
• Nitro Group Reduction 25%
• Indole Synthesis 25%
• Morpholine 25%
• Thioanisole 25%

Chemistry

• Heterocyclic Compound 100%
• 1,2-Dichloroethane 100%
• Chemical Ionization 66%
• Nitrobenzene 66%
• Radical Cation 66%
• Indole 66%
• Chemistry 33%
• Mass Spectrometry 33%
• Chemical Reactivity 33%
• Ethyl 33%
• Condensed Phase 33%
• Halide 33%
• Reduction 33%
• Sulfone 33%
• 1,3-dioxolane 33%
• Vinyl Ether 33%
• Nitro Group 33%
• Nucleophile 33%
• Collision Induced Dissociation 33%
• Collisionally Activated Dissociation (CAD) 33%
• Regioselectivity 33%
• Atmospheric Pressure Chemical Ionization 33%
• Morpholine 33%
• Thioanisole 33%