· Synthesis of 5,6-dicyanobenzofurans based on 4-bromo-5-nitrophthalonitrile / Zh. V. Chirkova, S. I. Filimonov, I. G. Abramov, S. I. Firgang, G. A. Stashina, A. S. Shashkov // Mendeleev Commun.. – 2009. – V. 19. – P. 332-333;
· Synthesis of 2-oxo- and 2-thioxo-5-(benzofuran-2-yl)tetrahydropyrimidines / Zh. V. Chirkova, S. I. Filimonov, I. G. Abramov, S. I. Firgang, G. A. Stashina // Mendeleev Commun. – 2011. – V. 21. – P. 46-47;
· Synthesis of novel substituted 4-hydroxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6,7-dicarbonitriles / Zh. V. Chirkova, S. I. Filimonov, I. G. Abramov, S. I. Firgang, G. A. Stashina, K. Yu. Suponitsky // Heterocycles. – 2011. - Vol. 83, N 4. – P 755-763;
· Base-induced transformations of orthonitrobenzylketones: Intramolecular displacement of nitro group versus nitro-nitrite rearrangement / S.I. Filimonov, Zh.V. Chirkova, I.G. Abramov, S. I. Firgang, G. A. Stashina, Yu.A. Strelenko, D. V. Khakimov, T. S. Pivina, A. V. Samet, K. Yu. Suponitsky // Tetrahedron – 2012. – Vol. 68, N 30. – P. 5991-5997;
· Synthesis of 3-substituted 2-amino-1-hydroxy-1H-Indole-5, 6-dicarbonitriles / S.I. Filimonov, Zh.V. Chirkova, V. S. Sharunov, I.G. Abramov, S. I. Firgang, G. A. Stashina, K. Yu. Suponitsky // Chem. Heterocycl. Compd. – 2012. Vol. 48, N 3. – P. 427-435;
· Inhibition of monoamine oxidase by indole-5,6-dicarbonitrile derivatives / Zh.V. Chirkova, M.V. Kabanova, S.I. Filimonov, I.G. Abramov, A. Petzer, J.P. Petzer, S.I. Firgang, K.Yu. Suponitsky // Bioorg. Med. Chem. Lett. - 2015. - Vol. 25, N 6. – P. 1206–1211;
· Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles / Zh.V. Chirkova, M.V. Kabanova, S.S. Sergeev, S.I. Filimonov, I.G. Abramov, A.V. Samet, K.Yu. Suponitsky // Mendeleev Commun. – 2015. - Vol. 25, N 4. – P. 315–317;
· An evaluation of synthetic indole derivatives as inhibitors of monoamine oxidase / Zh.V. Chirkova, M.V. Kabanova, S.I. Filimonov, I.G. Abramov, A. Petzer, J.P. Petzer, K.Yu. Suponitsky // Bioorg. Med. Chem. Lett. – 2016. – Vol. 26, N 9. – P. 2214–2219;
· Синтез функциональных производных индол-5,6-дикарбоновых и карбазол-2,3-дикарбоновых кислот / Ж.В. Чиркова, C.И. Филимонов // Изв. АН. Серия химическая – 2017. – Т. 66, № 3. – С. 379-394 (обзор);
· Синтез N-гидроксииндолов / Ж.В. Чиркова // Изв. вузов. Сер. Химия и хим. технология. – 2017. – Т. 60, № 4. – С. 4-20 (обзор);
· The C-3 acylation of 1-hydroxyindoles / Zh.V. Chirkova, M.V. Kabanova, S.I. Filimonov, I.G. Abramov, A.V. Samet, G.A. Stashina, K.Yu. Suponitsky // Tetrahedron Lett. – 2017. – Vol. 58, N 8. – P. 755–757;
· The С-3 chlorination of 1-hydroxyindoles / Zh.V. Chirkova, M.V. Kabanova, S.I. Filimonov, I.G. Abramov, A.V. Samet, G.A. Stashina // Mendeleev Commun. – 2017. – Vol. 27, N 5. – P. 498-499;
· Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles / Zh. V. Chirkova, S. I. Filimonov, I. G. Abramov // Mendeleev Commun. – 2018. – Vol. 28, N 1. – P. 86-87;
· An investigation of the monoamine oxidase inhibition properties of pyrrolo[3,4-f]indole-5,7-dione and indole-5,6-dicarbonitrile derivatives / Zh. V. Chirkova, M. V. Kabanova, S. I. Filimonov, I. G. Abramov, A. Petzer, I. Engelbrecht, J. P. Petzer, K. Yu. Suponitsky, A. V. Veselovsky // Drug Development Research. – 2018. - Vol. 38, N 2. - P. 81-93;
· Novel monoamine oxidase inhibitors based on the privileged 2-imidazoline molecular framework / A. Shetnev, A. Osipyan, S. Baykov, A. Sapegin, Zh. Chirkova, M. Korsakov, A. Petzer, I. Engelbrecht, J.P. Petzer // Bioorg. Med. Chem. Lett. – 2019. – Vol. 29, N 1. – P. 40–46.