Reactions of 1-Arylbenziodoxolones with Azide Anion: Experimental and Computational Study of Substituent Effects

Keyphrases

• Computational Study 100%
• Substituent Effect 100%
• Azide Anion 100%
• Benziodoxolones 100%
• Nucleophilic Substitution 66%
• Electron-withdrawing 66%
• Para-position 66%
• Substitution Rate 66%
• Iodine Atom 66%
• Ortho 33%
• Quantum Chemistry 33%
• Reaction Pathway 33%
• Nucleophile 33%
• Bromine 33%
• Benzene Ring 33%
• Nitro Group 33%
• Leaving Group 33%
• Electron-deficient 33%
• Bulky Substituents 33%
• Aryl Rings 33%
• Iodonium 33%
• Observed Effects 33%
• Benziodoxole 33%

Chemistry

• Substituent Effect 100%
• Nucleophilic Substitution 100%
• Iodine Atom 100%
• Azide Anion 100%
• Reaction Path 50%
• Benzene Ring 50%
• Nitro Group 50%
• Benziodoxole 50%
• Iodonium 50%
• Nucleophile 50%
• electronics 50%