Abstract:
Conditions under which a nitro group in 1,3,5-trinitrobenzene is replaced under the action of NH-azoles were found.
Document Type:
Article
Language: English
Citation:
O. Yu. Sapozhnikov, M. D. Dutov, M. A. Korolev, V. V. Kachala, S. A. Shevelev, “Substitution for a nitro group in 1,3,5-trinitrobenzene under the action of NH-azoles”, Mendeleev Commun., 11:6 (2001), 232–233
Linking options:
https://www.mathnet.ru/eng/mendc4310
https://www.mathnet.ru/eng/mendc/v11/i6/p232
This publication is cited in the following 14 articles:
Igor L. Dalinger, Alexandr V. Kormanov, Tatyana K. Shkineva, Aleksei B. Sheremetev, “Reactivity of Azasydnones: Unusual Diversity in Reactions of Chloro‐ and Nitrophenyl Derivatives with Nitrogen Nucleophiles”, Asian J Org Chem, 9:5 (2020), 811
Rosa M. Claramunt, Dolores Santa María, Ibon Alkorta, José Elguero, “The Structure ofN‐phenyl‐pyrazoles and Indazoles: Mononitro, Dinitro, and Trinitro Derivatives”, Journal of Heterocyclic Chem, 55:1 (2018), 44
M. D. Dutov, S. A. Shevelev, V. N. Koshelev, D. R. Aleksanyan, O. V. Serushkina, O. D. Neverova, E. V. Kolvina, E. S. Bobrov, “Dual reactivity of 1-chloro- and 1-bromo-3,5-dinitrobenzenes in aromatic nucleophilic substitution”, Mendeleev Commun., 27:2 (2017), 160–162
Alexey M. Starosotnikov, Vladislav V. Nikol'skiy, Anastasiya N. Borodulya, Vadim V. Kachala, Maxim A. Bastrakov, Vitaly N. Solkan, Svyatoslav A. Shevelev, “Synthesis and Functionalization of 5,7‐Dinitroquinoline and Its N‐Oxide”, Asian J Org Chem, 5:5 (2016), 685
Nataliya Belskaya, Julia Subbotina, Svetlana Lesogorova, Topics in Heterocyclic Chemistry, 40, Chemistry of 1,2,3-triazoles, 2014, 51
R. Chauhan, J. Dwivedi, A. A. Siddiqi Anees, D. Kishore, “Synthesis and antimicrobial activity of chalcone derivatives of indole nucleus”, Pharm Chem J, 44:10 (2011), 542
S. S. Vorob'ev, M. D. Dutov, I. A. Vatsadze, E. P. Petrosyan, V. V. Kachala, Yu. A. Strelenko, S. A. Shevelev, “Intramolecular cyclization of O-(3,5-dinitrophenyl) and O-(3-amino-5-nitrophenyl) ketoximes, products of transformations of 1,3,5-trinitrobenzene. The synthesis of nitrobenzo[b]furans and 4-hydroxynitroindoles”, Russ Chem Bull, 56:5 (2007), 1020
A. Kh. Shakhnes, S. S. Vorob'ev, S. A. Shevelev, “Selective reduction of one, two, or three nitro groups in 1,3,5-trinitrobenzene with hydrazine hydrate”, Russ Chem Bull, 55:5 (2006), 938
M. D. Dutov, S. S. Vorob'ev, O. V. Serushkina, S. A. Shevelev, B. I. Ugrak, V. V. Kachala, “Reactions of ortho-aminophenols and ortho-aminothiophenols with 1,3,5-trinitrobenzene”, Mendeleev Commun., 16:4 (2006), 230–232
O. Yu. Sapozhnikov, V. V. Dyachuk, M. D. Dutov, V. V. Kachala, S. A. Shevelev, “Synthesis of 2-aryl-6-nitro-4-(vic-triazol-1-yl)-1H-indoles from E-2,4,6-trinitrostilbenes”, Russ Chem Bull, 54:5 (2005), 1331
M. D. Dutov, I. A. Vatsadze, S. S. Vorob'ev, S. A. Shevelev, “Synthesis of 4,6-dinitrobenzo[b]furans from 1,3,5-trinitrobenzene”, Mendeleev Commun., 15:5 (2005), 202–204
Oleg Yu. Sapozhnikov, Mikhail D. Dutov, Maksim A. Korolev, Vadim V. Kachala, Svyatoslav A. Shevelev, “ChemInform Abstract: Substitution for a Nitro Group in 1,3,5‐Trinitrobenzene under the Action of NH‐Azoles.”, ChemInform, 33:23 (2002)
S. A. Shevelev, I. A. Vatsadze, M. D. Dutov, “Substitution for a nitro group in 1,3,5-trinitrobenzene and meta-substituted 1,3-dinitrobenzenes under the action of oximes”, Mendeleev Commun., 12:5 (2002), 196–198
O. Yu. Sapozhnikov, M. D. Dutov, V. V. Kachala, S. A. Shevelev, “Consecutive substitution for three nitro groups in 1,3,5-trinitrobenzene under the action of benzotriazole and other nucleophiles”, Mendeleev Commun., 12:6 (2002), 231–233
Contact us: