Аннотация:
A facile, diastereoselective method for the synthesis of diaziridines with C- and N-cyclopropyl substituents has been developed, N-cyclopropyldiaziridines being for the first time synthesized. The method is based on one-pot three-component condensation of cyclopropyl-containing carbonyl compounds, primary aliphatic amines including cyclopropylamine, and N-chloroalkylamines in organic solvents in the presence of bases under mild conditions.
Образец цитирования:
V. V. Kuznetsov, V. V. Kachala, N. N. Makhova, “Synthesis of hybrid structures comprising diaziridine and cyclopropane rings in one molecule”, Mendeleev Commun., 28:5 (2018), 497–500
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1813
https://www.mathnet.ru/rus/mendc/v28/i5/p497
Эта публикация цитируется в следующих 11 статьяx:
V.V. Kuznetsov, D.V. Khakimov, A.I. Samigullina, A.S. Dmitrenok, “Synthesis and physical properties of new 1,6-diazabicyclo[4.1.0]heptanes: Quantum-chemistry calculations and crystal structures simulations”, Chemical Physics, 579 (2024), 112187
Georgiy G. Ageev, Anatoliy N. Rykov, Olga E. Grikina, Igor F. Shishkov, Igor V. Kochikov, Vladimir V. Kuznetsov, Nina N. Makhova, Sergei S. Bukalov, “Equilibrium Molecular Structure of 3,3,6-trimethyl-1,5-diazabicyclo[3.1.0]hexane: the joint analysis of the gas-phase electron diffraction data and quantum chemical simulations”, Struct Chem, 33:1 (2022), 113
Kento Iwai, Khimiya Wada, Feiyue Hao, Haruyasu Asahara, Nagatoshi Nishiwaki, “A Mechanistic Study for Aziridination of Nitroalkenes Mediated by N-Chlorosuccinimide”, J. Oleo Sci., 71:6 (2022), 897
V.V. Kuznetsov, D.V. Khakimov, A.S. Dmitrenok, A.S. Goloveshkin, “Synthesis, structure and peculiarity of conformational behavior of 1,5-diazabicyclo[3.1.0]hexanes”, Journal of Molecular Structure, 1269 (2022), 133856
Inna Nikolaevna Kolesnikova, Vladimir Vladimirovich Kuznetsov, Alexander Sergeevich Goloveshkin, Nikolai Andreevich Chegodaev, Nina Nikolaevna Makhova, Igor Fedorovich Shishkov, “6,6′-Dimethyl-1,1′,5,5′-tetraaza-6,6′-bi(bicyclo[3.1.0]hexane): synthesis and investigation of molecular structure by quantum-chemical calculations, NMR spectroscopy and X-ray diffraction analysis”, Struct Chem, 32:6 (2021), 2303
Zetryana Puteri Tachrim, Lei Wang, Yuta Murai, Makoto Hashimoto, “New Trends in Diaziridine Formation and Transformation (a Review)”, Molecules, 26:15 (2021), 4496
Dmitry V. Khakimov, Leonid L. Fershtat, Tatyana S. Pivina, Nina N. Makhova, “Nitrodiaziridines: Unattainable yet, but Desired Energetic Materials”, J. Phys. Chem. A, 125:18 (2021), 3920
Sundaresan Ravindra, C. P. Irfana Jesin, Arivalagan Shabashini, Ganesh Chandra Nandi, “Recent Advances in the Preparations and Synthetic Applications of Oxaziridines and Diaziridines”, Adv Synth Catal, 363:7 (2021), 1756
Leonid S. Khaikin, Georgiy G. Ageev, Anatoliy N. Rykov, Olga E. Grikina, Igor F. Shishkov, Igor V. Kochikov, Vladimir V. Kuznetsov, Nina N. Makhova, Sergei S. Bukalov, Larisa A. Leites, “Equilibrium molecular structure and spectra of 6-methyl-1,5-diazabicyclo[3.1.0]hexane: joint analysis of gas phase electron diffraction, quantum chemistry, and spectroscopic data”, Phys. Chem. Chem. Phys., 22:39 (2020), 22477
L. S. Khaikin, G. G. Ageev, O. E. Grikina, I. F. Shishkov, V. V. Kuznetsov, N. N. Makhova, “Intramolecular Motions in 1,2,3-Triethyldiaziridine: A Quantum Chemistry Study”, Russ. J. Phys. Chem., 94:9 (2020), 1836
Н. Н. Махова, Л. И. Беленький, Г. А. Газиева, И. Л. Далингер, Л. С. Константинова, В. В. Кузнецов, А. Н. Кравченко, М. М. Краюшкин, О. А. Ракитин, А. М. Старосотников, Л. Л. Ферштат, С. А. Шевелев, В. З. Ширинян, В. Н. Яровенко, “Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем”, Усп. хим., 89:1 (2020), 55–124; N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124
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