The chemistry of heterocycles in the 21st century-Reference-Cited by-同舟云学术

The chemistry of heterocycles in the 21st century

Published:2024-07 Issue:7 Volume:93 Page:RCR5125
ISSN:0036-021X
Container-title:Russian Chemical Reviews
language:en
Short-container-title:RUSS CHEM REV

Author:

Charushin V. N.¹²^ORCID,Verbitskiy E. V.¹²^ORCID,Chupakhin O. N.¹²^ORCID,Vorobyeva D. V.³^ORCID,Gribanov P. S.³^ORCID,Osipov S. N.³^ORCID,Ivanov A. V.⁴^ORCID,Martynovskaya S. V.⁴^ORCID,Sagitova E. F.⁴^ORCID,Dyachenko V. D.⁵^ORCID,Dyachenko I. V.⁵^ORCID,Krivokolylsko S. G.⁶^ORCID,Dotsenko V. V.⁷⁸⁶^ORCID,Aksenov A. V.⁸^ORCID,Aksenov D. A.⁸^ORCID,Aksenov N. A.⁸^ORCID,Larin A. A.⁹^ORCID,Fershtat L. L.⁹^ORCID,Muzalevskiy V. M.¹⁰^ORCID,Nenajdenko V. G.¹⁰^ORCID,Gulevskaya A. V.¹¹^ORCID,Pozharskii A. F.¹¹^ORCID,Filatova E. A.¹¹^ORCID,Belyaeva K. V.⁴^ORCID,Trofimov B. A.⁴,Balova I. A.¹²^ORCID,Danilkina N. A.¹²^ORCID,Govdi A. I.¹²^ORCID,Tikhomirov A. S.¹³¹⁴^ORCID,Shchekotikhin A. E.¹³¹⁴^ORCID,Novikov M. S.¹²^ORCID,Rostovskii N. V.¹²^ORCID,Khlebnikov A. F.¹²^ORCID,Klimochkin Yu. N.¹⁵^ORCID,Leonova M. V.¹⁵^ORCID,Tkachenko I. M.¹⁵^ORCID,Mamedov V. A O.¹⁶^ORCID,Mamedova V. L.¹⁶^ORCID,Zhukova N. A.¹⁶^ORCID,Semenov V. E.¹⁶^ORCID,Sinyashin O. G.¹⁶^ORCID,Borshchev O. V.¹⁷^ORCID,Luponosov Yu. N.¹⁷^ORCID,Ponomarenko S. A.¹⁷^ORCID,Fisyuk A. S.¹⁸^ORCID,Kostyuchenko A. S.¹⁸^ORCID,Ilkin V. G.¹^ORCID,Beryozkina T. V.¹^ORCID,Bakulev V. A.¹^ORCID,Gazizov A. S.¹⁶^ORCID,Zagidullin A. A.¹⁶^ORCID,Karasik A. A.¹⁶^ORCID,Kukushkin M. E.¹⁰^ORCID,Beloglazkina E. K.¹⁰^ORCID,Golantsov N. E.¹⁹^ORCID,Festa A. A.¹⁹^ORCID,Voskresenskii L. G.¹⁹^ORCID,Moshkin V. S.¹^ORCID,Buev E. M.¹^ORCID,Sosnovskikh V. Ya.¹^ORCID,Mironova I. A.²⁰^ORCID,Postnikov P. S.²⁰^ORCID,Zhdankin V. V.²⁰,Yusubov M. S O.²⁰^ORCID,Yaremenko I. A.⁹^ORCID,Vil' V. A.⁹^ORCID,Krylov I. B.⁹^ORCID,Terent'ev A. O.⁹^ORCID,Gorbunova Yu. G.²¹²²^ORCID,Martynov A. G.²¹^ORCID,Tsivadze A. Yu.²¹²²^ORCID,Stuzhin P. A.²³^ORCID,Ivanova S. S.²³^ORCID,Koifman O. I.²³^ORCID,Burov O. N.¹¹^ORCID,Kletskii M. E.¹¹,Kurbatov S. V.¹¹,Yarovaya O. I.²⁴^ORCID,Volcho K. P.²⁴^ORCID,Salakhutdinov N. F.²⁴^ORCID,Panova M. A.²^ORCID,Burgart Ya. V.²^ORCID,Saloutin V. I.²^ORCID,Sitdikova A. R.²⁵^ORCID,Shchegravina E. S.²⁵^ORCID,Fedorov A. Yu.²⁵^ORCID

Affiliation:

1. Ural Federal University named after the first President of Russia B.N.Yeltsin, Ekaterinburg, Russian Federation

2. I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

3. A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation

4. A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation

5. Lugansk State Pedagogical University, Lugansk, Russian Federation

6. Vladimir Dahl Lugansk State University, Lugansk, Russian Federation

7. Kuban State University, Krasnodar, Russian Federation

8. North Caucasus Federal University, Stavropol, Russian Federation

9. N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

10. Faculty of Chemistry, Lomonosov Moscow State University, Moscow, Russian Federation

11. Department of Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation

12. Institute of Chemistry, Saint Petersburg State University, Saint Petersburg, Russian Federation

13. Gause Institute of New Antibiotics, Moscow, Russian Federation

14. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation

15. Samara State Technical University, Samara, Russian Federation

16. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Kazan, Russian Federation

17. Enikolopov Institute of Synthetic Polymeric Materials, Russian Academy of Sciences, Moscow, Russian Federation

18. Dostoevsky Omsk State University, Omsk, Russian Federation

19. Peoples' Friendship University of Russia named after Patrice Lumumba (RUDN University), Moscow, Russian Federation

20. National Research Tomsk Polytechnic University, Tomsk, Russian Federation

21. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

22. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Moscow, Russian Federation

23. Institute of Macroheterocyclic Compounds, Ivanovo State University of Chemistry and Technology, Russian Federation

24. N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

25. Faculty of Chemistry, N.I. Lobachevskii Nizhnii Novgorod State University, Nizhnii Novgorod, Russian Federation

Abstract

The chemistry of heterocyclic compounds has traditionally been and remains a bright area of chemical science in Russia. This is due to the fact that many heterocycles find the widest application. These compounds are the key structural fragments of most drugs, plant protection agents. Many natural compounds are also derivatives of heterocycles. At present, more than half of the hundreds of millions of known chemical compounds are heterocycles. This collective review is devoted to the achievements of Russian chemists in this field over the last 15–20 years. The review presents the achievements of leading heterocyclists representing both RAS institutes and university science. It is worth noting the wide scope of the review, both in terms of the geography of author teams, covering the whole of our large country, and in terms of the diversity of research areas. Practically all major types of heterocycles are represented in the review. The special attention is focused on the practical applications of heterocycles in the design of new drugs and biologically active compounds, high-energy molecules, materials for organic electronics and photovoltaics, new ligands for coordination chemistry, and many other rapidly developing areas. These practical advances would not be possible without the development of new fundamental transformations in heterocyclic chemistry.<br> Bibliography — 2237 references.

Publisher

Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii

Reference2235 articles.

1. Semiconducting π-Conjugated Systems in Field-Effect Transistors: A Material Odyssey of Organic Electronics

2. Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds: Synthetic Routes, Properties, and Applications

3. Recent Advances in Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds

4. G.V.Zaryanov, G.N.Lipunova, E.V.Nosova, O.S.Taniya, D.S.Kopchuk. Push-pulnue Fluorofory Azinovogo Ryada. Chast 1. Proizvodnye Monoazinov i ikh Annelirovannye Analogi. (Push-pull Fluorophores of the Azine Series. Part 1. Monoazine Derivatives and their Annelated Analogues). (Ekaterinburg: Izd. AMB, 2022). 240 p.

5. E.V.Verbitskiy, G.N.Lipunova, E.V.Nosova, G.V.Zaryanov, V.N.Charushin. Push-pulnue Fluorofory Azinovogo Ryada. Chast 2. Aziny s Dbumya i Bolee Atomami Azota i ikh Annelirovannye Analogi. (Push-pull Fluorophores of the Azine Series. Part 2. Azines with Two or More Nitrogen Atoms and their Annelated Analogues). (Ekaterinburg: UB RAS, 2023). 428 p.

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis, enantiomeric composition, separation of (L)-menthyl 3-arylglycidates and their reactions with benzene-1,2-diamine;Tetrahedron;2024-09