1. Radomir Jasiński, “Synthesis of 1,2-oxazine N-oxides via noncatalyzed hetero-Diels–Alder reactions of nitroalkenes (microreview)”, Chem Heterocycl Comp, 60:3-4 (2024), 121  crossref
  2. Manzarbanou Asnaashariisfahani, Bayan Azizi, Mohammad Reza Poor Heravi, Sepideh Habibzadeh, Abdol Ghaffar Ebadi, Sheida Ahmadi, “Stereoselective cycloaddition of biologically active thioindoline with the smallest nanocage in gas phase versus solution via density functional theory”, J of Physical Organic Chem, 35:9 (2022)  crossref
  3. Max M. Majireck, John M. Bennett, Comprehensive Heterocyclic Chemistry IV, 2022, 283  crossref
  4. Radomir Jasiński, “On the Question of Stepwise [4+2] Cycloaddition Reactions and Their Stereochemical Aspects”, Symmetry, 13:10 (2021), 1911  crossref
  5. Agnieszka Kącka-Zych, Radomir Jasiński, “Molecular mechanism of Hetero Diels-Alder reactions between (E)-1,1,1-trifluoro-3-nitrobut-2-enes and enamine systems in the light of Molecular Electron Density Theory”, Journal of Molecular Graphics and Modelling, 101 (2020), 107714  crossref
  6. Agnieszka Kącka-Zych, “Participation of Phosphorylated Analogues of Nitroethene in Diels–Alder Reactions with Anthracene: A Molecular Electron Density Theory Study and Mechanistic Aspect”, Organics, 1:1 (2020), 36  crossref
  7. Radomir Jasiński, “β-Trifluoromethylated nitroethenes in Diels-Alder reaction with cyclopentadiene: A DFT computational study”, Journal of Fluorine Chemistry, 206 (2018), 1  crossref
  8. Irina Kostiv, “Investigation of the reaction mechanism of [4 + 2] cyclization of 2,3 dimethylbuta-1,3-diene to methylacrylate using the Michaelis-Menten equation”, Fr. Ukr. J. Chem., 6:1 (2018), 74  crossref
  9. Alexey Yu. Barkov, Nikolay S. Zimnitskiy, Igor B. Kutyashev, Vladislav Yu. Korotaev, Vladimir S. Moshkin, Vyacheslav Ya. Sosnovskikh, “Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: Synthesis of trihalomethylated spiroindenepyrroli(zi)dines”, Journal of Fluorine Chemistry, 204 (2017), 37  crossref
  10. Vladislav Y. Korotaev, Igor B. Kutyashev, Alexey Y. Barkov, Vyacheslav Y. Sosnovskikh, “Highly diastereoselective synthesis of novel 2,3,4-trisubstituted chromanes via the reaction of 3-nitro-2-(trihalomethyl)- and 3-nitro-2-phenyl-2 H -chromenes with 1-morpholinocyclopentene”, Tetrahedron, 73:34 (2017), 5122  crossref
  11. Alexey Yu. Barkov, Nikolay S. Zimnitskiy, Vladislav Yu. Korotaev, Igor B. Kutyashev, Vladimir S. Moshkin, Vyacheslav Ya. Sosnovskikh, “Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: synthesis of trihalomethylated spiro[indoline-3,2′-pyrrolidin]-2-ones and spiro[indoline-3,3′-pyrrolizin]-2-ones”, Tetrahedron, 72:43 (2016), 6825  crossref
  12. Radomir Jasiński, “First example of stepwise, zwitterionic mechanism for bicyclo[2.2.1]hept-5-ene (norbornene) formation process catalyzed by the 1-butyl-3-methylimidazolium cations”, Monatsh Chem, 147:7 (2016), 1207  crossref
  13. Radomir Jasiński, “A reexamination of the molecular mechanism of the Diels–Alder reaction between tetrafluoroethene and cyclopentadiene”, Reac Kinet Mech Cat, 119:1 (2016), 49  crossref
  14. V. Yu. Korotaev, V. Ya. Sosnovskikh, A. Yu. Barkov, P. A. Slepukhin, Yu. V. Shklyaev, “Synthesis of 1-hetaryl-5,6-dihydropyrrolo[2,1-a]isoquinolines from 1-hetarylmethyl-3,4-dihydroisoquinolines and 1,1,1-trifluoro-3-nitrobut-2-ene”, Russ Chem Bull, 64:4 (2015), 891  crossref
  15. Vladislav Yu. Korotaev, Alexey Yu. Barkov, Evgeniya G. Matochkina, Mikhail I. Kodess, Vyacheslav Ya. Sosnovskikh, “Synthesis of chromeno[3,4-c][1,2]oxazine-N-oxides via formal [4+2] cycloaddition of 3-nitro-2-trihalomethyl-2H-chromenes with cyclohexanone and pinacolone enamines”, Tetrahedron, 70:34 (2014), 5161  crossref
  16. Radomir Jasiński, Magdalena Kubik, Agnieszka Łapczuk-Krygier, Agnieszka Kącka, Ewa Dresler, Anna Boguszewska-Czubara, “An experimental and theoretical study of the hetero Diels–Alder reactions between (E)-2-aryl-1-cyano-1-nitroethenes and ethyl vinyl ether: one-step or zwitterionic, two-step mechanism?”, Reac Kinet Mech Cat, 113:2 (2014), 333  crossref
  17. Agnieszka Łapczuk-Krygier, Vladislav Yu. Korotaev, Alexey Yu. Barkov, Vyacheslav Ya. Sosnovskikh, Ewa Jasińska, Radomir Jasiński, “A DFT computational study on the molecular mechanism of the nitro group migration in the product derived from 3-nitro-2-(trifluoromethyl)-2 H -chromene and 2-(1-phenylpropylidene)malononitrile”, Journal of Fluorine Chemistry, 168 (2014), 236  crossref
  18. Radomir Jasiński, Magda Ziółkowska, Oleh Demchuk, Agata Maziarka, “Regio- and stereoselectivity of polar [2+3] cycloaddition reactions between (Z)-C-(3,4,5-trimethoxyphenyl)-N-methylnitrone and selected (E)-2-substituted nitroethenes”, Open Chemistry, 12:5 (2014), 586  crossref
  19. Radomir Jasiński, “Searching for zwitterionic intermediates in Hetero Diels–Alder reactions between methyl α,p-dinitrocinnamate and vinyl-alkyl ethers”, Computational and Theoretical Chemistry, 1046 (2014), 93  crossref
  20. Luis R. Domingo, “A new C–C bond formation model based on the quantum chemical topology of electron density”, RSC Adv., 4:61 (2014), 32415  crossref
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