An aniline dication-like transition state in the Bamberger rearrangement

Scholarly Works

• Lu, J.; Tang, K.; Qi, G.; Juan, C.; Xu, J.; Cai, Z.; Li, D.; Cai, X.; Liu, X.; Chen, M.; Ding, W.; Zhu, Y. Exclusive catalytic hydrogenation of nitrobenzene toward p-aminophenol over atomically precise Au36(SR)24 clusters. Chemical science 2024, 15, 15617–15624. doi:10.1039/d4sc05018e
• Dhandabani, G. K.; Chang, L.-T.; Hsieh, H.-Y.; Shih, C.-L.; Hsin, L.-W. One-pot tandem reduction and site-selective halogenation of nitroarenes. Organic & biomolecular chemistry 2024, 22, 976–981. doi:10.1039/d3ob01732j
• Nakamura, I. Cu-catalyzed [1,3]-Alkoxy Rearrangement Reactions of N-Alkoxyaniline Derivatives. Journal of Synthetic Organic Chemistry, Japan 2023, 81, 2–13. doi:10.5059/yukigoseikyokaishi.81.2
• Sochnev, V. S.; Kuz'menko, T. A.; Morkovnik, A. S.; Koshchienko, Y. V. Specific Features of the Reduction of 7-Nitro-9-R-2,3-dihydroimidazo[1,2-a]benzimidazoles with SnCl2 in Hydrochloric Acid. Russian Journal of Organic Chemistry 2022, 58, 679–684. doi:10.1134/s1070428022050062
• Boddapati, S. N. M.; Tamminana, R.; Alam, M. M.; Gugulothu, S.; Varala, R.; Bollikolla, H. B. Efficient Pd(II)-catalyzed regioselective ortho-halogenation of arylcyanamides. New Journal of Chemistry 2021, 45, 17176–17182. doi:10.1039/d1nj01998h
• De, S. K. doi:10.1002/9783527828166.ch1
• de Fonzo, N.; Quartarone, G.; Ronchin, L.; Tortato, C.; Vavasori, A. Kinetics and mechanistic study of the Bamberger rearrangement of N-phenylhydroxylamine to 4-aminophenol in acetonitrile-trifluoroacetic acid: A substrate acid complex as para selectivity driver. Applied Catalysis A: General 2016, 516, 58–69. doi:10.1016/j.apcata.2016.02.020
• Yamabe, S.; Yamazaki, S. A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid. Journal of Physical Organic Chemistry 2016, 29, 361–367. doi:10.1002/poc.3543
• Snape, T. J. Arene Chemistry; Wiley, 2015; pp 485–510. doi:10.1002/9781118754887.ch18
• van der Werf, A.; Selander, N. Para-Selective Halogenation of Nitrosoarenes with Copper(II) Halides. Organic letters 2015, 17, 6210–6213. doi:10.1021/acs.orglett.5b03198
• Yamabe, S.; Zeng, G.; Guan, W.; Sakaki, S. Proton transfers in the Strecker reaction revealed by DFT calculations. Beilstein journal of organic chemistry 2014, 10, 1765–1774. doi:10.3762/bjoc.10.184
• Liu, S.; Hao, Y.; Jiang, J. Bamberger Rearrangement of N-Arylhydroxylamine to p-Aminophenol in a CO2–H2O System. Industrial & Engineering Chemistry Research 2014, 53, 8372–8375. doi:10.1021/ie500864p

Explore citations to this article at