Molecular rearrangements of superelectrophiles

Scholarly Works

• Alam, S.; Khan, M. I.; Fiaz, F.; Iqbal, M. Z.; Alam, F.; Ahmad, Z.; Hegazy, H. H. Advancements in asymmetric supercapacitors: Material selection, mechanisms, and breakthroughs with metallic oxides, sulfides, and phosphates. Journal of Energy Storage 2023, 72, 108208. doi:10.1016/j.est.2023.108208
• Holmin, G. P.; Hood, J. C.; Scanlon, N.; Klumpp, D. A. Phosphonium-carbenium and oxophosphonium-carbenium dications in Friedel-Crafts reactions. Tetrahedron 2022, 121, 132928. doi:10.1016/j.tet.2022.132928
• Biddle, T. J.; Wermuth, U. D.; Loughlin, W. A.; Cresswell, S. L.; White, A. R. Potential forensic markers from synthetic pathways to 1-phenyl-2-propanone from uncontrolled and controlled substances. Forensic Chemistry 2022, 28, 100410. doi:10.1016/j.forc.2022.100410
• Vuong, H.; Amadou, H.; Stentzel, M. R.; Klumpp, D. A. Superelectrophilic nazarov cyclizations with N-heterocycles. Tetrahedron 2020, 76, 131644. doi:10.1016/j.tet.2020.131644
• Klumpp, D. A.; Anokhin, M. V. Superelectrophiles: Recent Advances. Molecules (Basel, Switzerland) 2020, 25, 3281. doi:10.3390/molecules25143281
• Fung, J.; Duong, T.-V.; Braceros, K. C. A.; Brooks, M. L.; Schloesser-Lingscheit, K.; Tagawa, T. K. S.; Wilson, J. M.; Jones, K. K.; Valente, E. J. Arylpyran Pseudoacid Racemization: Rate Estimation and Structural Influences. Journal of Chemical Crystallography 2020, 51, 14–41. doi:10.1007/s10870-020-00829-2
• Smaoui, A.; Essalah, K.; Boubaker, T.; Assfeld, X.; Picaud, F.; Tangour, B. First-principles study of the reaction mechanism governing the SNAr of the dimethylamine on 2-methoxy-5-nitrothiophenes. Theoretical Chemistry Accounts 2019, 139, 1–14. doi:10.1007/s00214-019-2519-x
• Fujita, H.; Kakuyama, S.; Fukuyoshi, S.; Hayakawa, N.; Oda, A.; Kunishima, M. Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species. The Journal of organic chemistry 2018, 83, 4568–4580. doi:10.1021/acs.joc.8b00331
• Kazakova, A. N.; Vasilyev, A. V. Trifluoromethanesulfonic acid in organic synthesis. Russian Journal of Organic Chemistry 2017, 53, 485–509. doi:10.1134/s1070428017040017
• Lin, D.; Wei, Y.; Ou, C.; Huang, H.; Xie, L.; Tang, L.; Huang, W. Carbon Cationic Relay via Superelectrophiles: Synthesis of Spiro-diazafluorenes. Organic letters 2016, 18, 6220–6223. doi:10.1021/acs.orglett.6b02595
• Gasonoo, M.; Naredla, R. R.; Lill, S. O. N.; Klumpp, D. A. Tetra- and Pentacationic Electrophiles and Their Chemistry. The Journal of organic chemistry 2016, 81, 11758–11765. doi:10.1021/acs.joc.6b02220
• Мikhal´chenko, L. V.; Leibzon, V. N.; Leonova, M. Y.; Gul'tyai, V. P. Effect of medium acidity on the efficiency of oxidation of 2,4,6-trinitrotoluene to 2,4,6-trinitrobenzoic acid. Russian Chemical Bulletin 2016, 65, 2216–2219. doi:10.1007/s11172-016-1571-0
• Coxon, J. M. doi:10.1002/9781118560273.ch13
• McClelland, R. A. doi:10.1002/9781118560273.ch7
• Kovacevic, L. S.; Idziak, C.; Markevicius, A.; Scullion, C.; Corr, M. J.; Kennedy, A. R.; Tuttle, T.; Murphy, J. A. Superelectrophilic Amidine Dications: Dealkylation by Triflate Anion. Angewandte Chemie 2012, 124, 8644–8647. doi:10.1002/ange.201202990
• Kovacevic, L. S.; Idziak, C.; Markevicius, A.; Scullion, C.; Corr, M. J.; Kennedy, A. R.; Tuttle, T.; Murphy, J. A. Superelectrophilic amidine dications: dealkylation by triflate anion. Angewandte Chemie (International ed. in English) 2012, 51, 8516–8519. doi:10.1002/anie.201202990
• Klumpp, D. A. Molecular Rearrangements of Superelectrophiles. ChemInform 2011, 42. doi:10.1002/chin.201138249

Explore citations to this article at