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Mendeleev Communications, 2015, Volume 25, Issue 4, Pages 312–314
DOI: https://doi.org/10.1016/j.mencom.2015.07.029
(Mi mendc2393)
 

This article is cited in 25 scientific papers (total in 25 papers)

Communications

New bis-o-quinone with azine spacer and its cyclization into indazolo[2,1-a]indazole system

M. V. Arsenyevab, E. V. Baranovab, A. Yu. Fedorovb, S. A. Chesnokova, G. A. Abakumovab

a G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhnii Novgorod, Russian Federation
b N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, Russian Federation
Abstract: Reaction of 4,6-di-tert-butyl-2,3-dyhydroxybenzaldehyde with hydrazine gives a new sterically hindered bis-catecholimine which on oxidation and heating undergoes cyclization into indazolo[2,1-a]indazole derivative.
Document Type: Article
Language: English


Citation: M. V. Arsenyev, E. V. Baranov, A. Yu. Fedorov, S. A. Chesnokov, G. A. Abakumov, “New bis-o-quinone with azine spacer and its cyclization into indazolo[2,1-a]indazole system”, Mendeleev Commun., 25:4 (2015), 312–314
Linking options:
  • https://www.mathnet.ru/eng/mendc2393
  • https://www.mathnet.ru/eng/mendc/v25/i4/p312
  • This publication is cited in the following 25 articles:
    1. Azamat Bikmukhametov, Natalia Vasilevskaya, Maxim Arsenyev, Alexander Gerasimov, Mikhail Bukharov, Daut Islamov, Svetlana Belyakova, Yury Kuzin, Gennady Evtugyn, Pavel Padnya, Ivan Stoikov, “Task-specific ionic liquid and organic salts based on catechol-containing hydrazones: Synthesis, selective Cu(II) binding, thermal properties, and redox-activity”, Journal of Molecular Liquids, 425 (2025), 127234  crossref
    2. A. V. Bogdanov, A. V. Samorodov, Z. A. Valiullina, N. I. Akylbekov, A. D. Voloshina, A. P. Lyubina, S. K. Amerkhanova, A. M. Saitova, T. N. Pashirova, O. M. Tsivileva, V. F. Mironov, “Biologically Active Ammonium Isatin-3-acylhydrazones Bearing Long-Chain Alkyl Substituent of Various Structures”, Russ J Gen Chem, 94:3 (2024), 539  crossref
    3. M. A. Zherebtsov, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, “Synthesis and Structure of an o-Quinone Based Cuban Copper Complex with a Benzoxazole Substituent”, J Struct Chem, 64:11 (2023), 2051  crossref
    4. M. A. Zherebtsov, M. V. Arsenyev, N. M. Khamaletdinova, E. V. Baranov, S. A. Chesnokov, “Di-tert-alkyl-substituted catechols with an imidazole substituent: synthesis, structure, and properties”, Russ Chem Bull, 72:9 (2023), 2102  crossref
    5. A. V. Bogdanov, S. V. Bukharov, R. A. Garifullina, A. D. Voloshina, A. P. Lyubina, S. K. Amerkhanova, M. S. Bezsonova, Z. Yu. Khaptsev, O. M. Tsivileva, “Synthesis and Antimicrobial Activity Evaluation of Ammonium Acylhydrazones Based on 4,6-Di-tert-butyl-2,3-dihydroxybenzaldehyde”, Russ J Gen Chem, 92:10 (2022), 1875  crossref
    6. M. A. Zherebtsov, E. R. Zhiganshina, N. A. Lenshina, R. S. Kovylin, E. V. Baranov, N. Yu. Shushunova, M. P. Shurygina, M. V. Arsenyev, S. A. Chesnokov, V. K. Cherkasov, “Synthesis and photoinitiating ability of substituted 4,5-di-tert-alkyl-o-benzoquinones in radical polymerization”, Russ Chem Bull, 70:4 (2021), 780  crossref
    7. Pavel Padnya, Ksenia Shibaeva, Maxim Arsenyev, Svetlana Baryshnikova, Olga Terenteva, Igor Shiabiev, Artur Khannanov, Artur Boldyrev, Alexander Gerasimov, Denis Grishaev, Yurii Shtyrlin, Ivan Stoikov, “Catechol-Containing Schiff Bases on Thiacalixarene: Synthesis, Copper (II) Recognition, and Formation of Organic-Inorganic Copper-Based Materials”, Molecules, 26:8 (2021), 2334  crossref
    8. M. A. Zherebtsov, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, V. K. Cherkasov, “Synthesis and structure of sterically hindered o-benzoquinone carboxylic acid”, Mendeleev Commun., 31:2 (2021), 268–270  mathnet  crossref
    9. M. A. Zherebtsov, M. V. Arsenyev, S. A. Chesnokov, V. K. Cherkasov, “Synthesis of 1-Substituted 5,5,8,8-Tetramethyl5,6,7,8-tetrahydronaphthalene-2,3-diols and 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalene-2,3-dione”, Russ J Org Chem, 56:3 (2020), 534  crossref
    10. Tatiana V. Astaf'eva, Maxim V. Arsenyev, Roman V. Rumyantcev, Georgy K. Fukin, Vladimir K. Cherkasov, Andrey I. Poddel'sky, “Imine-Based Catechols and o-Benzoquinones: Synthesis, Structure, and Features of Redox Behavior”, ACS Omega, 5:35 (2020), 22179  crossref
    11. Andrei V. Bogdanov, Kamilla R. Iskhakova, Alexandra D. Voloshina, Anastasia S. Sapunova, Natalia V. Kulik, Natalia V. Terekhova, Maxim V. Arsenyev, Guzel K. Ziyatdinova, Sergey V. Bukharov, “Ammonium‐Charged Sterically Hindered Phenols with Antioxidant and Selective Anti‐Gram‐Positive Bacterial Activity”, Chemistry & Biodiversity, 17:5 (2020)  crossref
    12. Margarita P. Shurygina, Maria Yu. Zakharina, Maxim A. Baten'kin, Alexey N. Konev, Andrey S. Shavyrin, Egor A. Chelnokov, Nataliya Yu. Shushunova, Maxim V. Arsenyev, Sergey A. Chesnokov, Gleb A. Abakumov, “A blue to red light sensitive photoinitiating systems based on 3,5-di-tert-butyl-o-benzoquinone derivatives for free radical polymerization”, European Polymer Journal, 127 (2020), 109573  crossref
    13. S. Yu. Bukhvalova, E. R. Zhiganshina, T. V. Astaf'eva, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, A. I. Poddel'sky, “New Sterically Hindered Bis-o-Benzoquinones with Electron-Donor Bridging Groups and Related Binuclear Triphenylantimony(V) Catecholate Complexes”, Russ J Coord Chem, 46:12 (2020), 817  crossref
    14. Thomas H. Do, Seth N. Brown, “Mono- and bimetallic pentacoordinate silicon complexes of a chelating bis(catecholimine) ligand”, Dalton Trans., 48:30 (2019), 11565  crossref
    15. Ligia R. Gomes, John N. Low, Nathasha R. de L. Correira, Thais C.M. Noguiera, Alessandra C. Pinheiro, Marcus V.N. de Souza, James L. Wardell, Solange M.S.V. Wardell, “Crystal structures and Hirshfeld surface analysis of four 1,4-bis(methoxyphenyl)-2,3-diazabuta-1,3-dienes: comparisons of the intermolecular interactions in related compounds”, Zeitschrift für Kristallographie - Crystalline Materials, 234:1 (2019), 59  crossref
    16. E. R. Zhiganshina, M. V. Arsenyev, A. S. Shavyrin, E. V. Baranov, S. A. Chesnokov, “Trans-etherification of catechol-type benzylic ether with diols as a route to new sterically hindered bis-catechols”, Mendeleev Commun., 29:1 (2019), 91–93  mathnet  crossref
    17. M. V. Arsen'ev, L. S. Okhlopkova, A. I. Poddel'skii, G. K. Fukin, “Binuclear Triphenylantimony(V) Catecholate Based on Redox-Active Bis-o-Benzoquinone, a Bis-Catechol-Aldimine Derivative”, Russ J Coord Chem, 44:2 (2018), 162  crossref
    18. M. V. Arsenyev, T. V. Astaf'eva, E. V. Baranov, A. I. Poddel'sky, S. A. Chesnokov, “New sterically hindered bis-catechol, bis-o-quinone and its bis-triphenylantimony(v) bis-catecholate. 3,5-Di-tert-butyl-6-methoxymethylcatechol as alkylating agent”, Mendeleev Commun., 28:1 (2018), 76–78  mathnet  crossref
    19. Andrey I. Poddel'sky, Maxim V. Arsenyev, Tatyana V. Astaf'eva, Sergey A. Chesnokov, Georgy K. Fukin, Gleb A. Abakumov, “New sterically-hindered 6th-substituted 3,5-di- tert -butylcatechols/ o -quinones with additional functional groups and their triphenylantimony(V) catecholates”, Journal of Organometallic Chemistry, 835 (2017), 17  crossref
    20. A. I. Poddel'sky, M. V. Arsen'ev, L. S. Okhlopkova, I. V. Smolyaninov, G. K. Fukin, “New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group”, Russ J Coord Chem, 43:12 (2017), 843  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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