Microwave assisted cycloaddition of benzonitrile oxides to 1-iodobuta-1,3-diynes

Ефремова, М. М., Хашимова, Д. Д., Калинин, Н. С., Штыров, А. А., Рязанцев, М. Н., Спиридонова, Д. В., Говди, А. И. & Балова, И. А., 1 Jul 2024, In: Mendeleev Communications. 34, 4, p. 536-539 4 p.

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The chemistry of heterocycles in the 21st century

Charushin, V. N., Verbitskiy, E. V., Chupakhin, O. N., Vorobyeva, D. V., Gribanov, P. S., Osipov, S. N., Ivanov, A. V., Martynovskaya, S. V., Sagitova, E. F., Dyachenko, V. D., Dyachenko, I. V., Krivokolylsko, S. G., Dotsenko, V. V., Aksenov, A. V., Aksenov, D. A., Aksenov, N. A., Larin, A. A., Fershtat, L. L., Muzalevskiy, V. M., Nenajdenko, V. G. & 66 others, Gulevskaya, A. V., Pozharskii, A. F., Filatova, E. A., Belyaeva, K. V., Trofimov, B. A., Balova, I. A., Danilkina, N. A., Govdi, A. I., Tikhomirov, A. S., Shchekotikhin, A. E., Novikov, M. S., Rostovskii, N. V., Khlebnikov, A. F., Klimochkin, Y. N., Leonova, M. V., Tkachenko, I. M., Mamedov, V. A. O., Mamedova, V. L., Zhukova, N. A., Semenov, V. E., Sinyashin, O. G., Borshchev, O. V., Luponosov, Y. N., Ponomarenko, S. A., Fisyuk, A. S., Kostyuchenko, A. S., Ilkin, V. G., Beryozkina, T. V., Bakulev, V. A., Gazizov, A. S., Zagidullin, A. A., Karasik, A. A., Kukushkin, M. E., Beloglazkina, E. K., Golantsov, N. E., Festa, A. A., Voskresenskii, L. G., Moshkin, V. S., Buev, E. M., Sosnovskikh, V. Y., Mironova, I. A., Postnikov, P. S., Zhdankin, V. V., Yusubov, M. S. O., Yaremenko, I. A., Vil', V. A., Krylov, I. B., Terent'ev, A. O., Gorbunova, Y. G., Martynov, A. G., Tsivadze, A. Y., Stuzhin, P. A., Ivanova, S. S., Koifman, O. I., Burov, O. N., Kletskii, M. E., Kurbatov, S. V., Yarovaya, O. I., Volcho, K. P., Salakhutdinov, N. F., Panova, M. A., Burgart, Y. V., Saloutin, V. I., Sitdikova, A. R., Shchegravina, E. S. & Fedorov, A. Y., 1 Jul 2024, In: Russian Chemical Reviews. 93, 7, RCR5125.

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Facile synthesis of diiodoheteroindenes and understanding their Sonogashira cross-coupling selectivity for the construction of unsymmetrical enediynes

Пономарев, А. В., Данилкина, Н. А., Окунева, Ю. С., Видякина, А. А., Хмелевская, Е. А., Бунев, А. С., Румянцев, А. М., Говди, А. И., Suarez, T., Алабугин, И. & Балова, И. А., 24 Apr 2024, In: Organic and Biomolecular Chemistry. 22, 20, p. 4096-4107 12 p.

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Docking and Molecular Dynamics Studies on DNA-Heterocyclic Enediynes Interaction to Identify the Preferred Binding Mode

Гуреев, М. А., Данилкина, Н. А., Хлебников, А. Ф. & Балова, И. А., 21 Mar 2024, In: Russian Journal of General Chemistry. 94, Suppl 1, p. S100-S119

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Cu-catalyzed cycloaddition of aryl azides to 1-iodobuta-1,3-diynes: an experimental and quantum chemical study of unusual regiochemistry

Govdi, A. I., Danilkina, N. A., Shtyrov, A. A., Ryazantsev, M. N., Kim, M. D., Kryukova, M. A. & Balova, I. A., 2024, In: New Journal of Chemistry.

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The green chemistry paradigm in modern organic synthesis

Zlotin, S. G., Egorova, K. S., Ananikov, V. P., Akulov, A. A., Varaksin, M. V., Chupakhin, O. N., Charushin, V. N., Bryliakov, K. P., Averin, A. D., Beletskaya, I. P., Dolengovski, E. L., Budnikova, Y. H., Sinyashin, O. G., Gafurov, Z. N., Kantyukov, A. O., Yakhvarov, D. G., Aksenov, A. V., Elinson, M. N., Nenajdenko, V. G., Chibiryaev, A. M. & 20 others, Nesterov, N. S., Kozlova, E. A., Martyanov, O. N., Balova, I. A., Sorokoumov, V. N., Guk, D. A., Beloglazkina, E. K., Lemenovskii, D. A., Chukicheva, I. Y., Frolova, L. L., Izmest'ev, E. S., Dvornikova, I. A., Popov, A. V., Kutchin, A. V., Borisova, D. M., Kalinina, A. A., Muzafarov, A. M., Kuchurov, I. V., Maximov, A. L. & Zolotukhina, A. V., 1 Dec 2023, In: Russian Chemical Reviews. 92, 12, RCR5104.

Research output: Contribution to journal › Review article › peer-review

Development of Fluorescent Isocoumarin‐Fused Oxacyclononyne – 1,2,3‐Triazole Pairs

Vidyakina, A. A., Shtyrov, A. A., Ryazantsev, M. N., Khlebnikov, A. F., Kolesnikov, I. E., Sharoyko, V. V., Spiridonova, D. V., Balova, I. A., Bräse, S. & Danilkina, N. A., 9 Jun 2023, (E-pub ahead of print) In: Chemistry - A European Journal. e202300540.

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