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Mendeleev Communications, 2021, Volume 31, Issue 2, Pages 262–264
DOI: https://doi.org/10.1016/j.mencom.2021.03.040
(Mi mendc900)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Utilizing o-quinone methide chemistry: synthesis of sterically hindered acridin-4-ols

S. K. Polyakovaab, T. V. Balashovaa, R. V. Rumyantceva, M. V. Arsenyevab, G. K. Fukina, S. A. Chesnokova

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
Full-text PDF (540 kB) Citations (8)
Abstract: Three new sterically hindered acridin-4-ols have been prepared by alkylation of anilines with 3,5-di-tert-butyl-6-methoxymethylcatechol followed by oxidation of the reaction mixture. Formation of the acridine moiety was found to occur in the course of oxidation of the intermediate (anilinomethyl)catechol on contact with air in the Et2O/H2O–KOH system. The molecular structure of two acridin-4-ols was determined by single-crystal X-ray diffraction.
Keywords: acridines, heterocyclization, quinone methides, alkylation, catechols, anilines, X-ray diffraction analysis.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (765.9 Kb)


Citation: S. K. Polyakova, T. V. Balashova, R. V. Rumyantcev, M. V. Arsenyev, G. K. Fukin, S. A. Chesnokov, “Utilizing o-quinone methide chemistry: synthesis of sterically hindered acridin-4-ols”, Mendeleev Commun., 31:2 (2021), 262–264
Linking options:
  • https://www.mathnet.ru/eng/mendc900
  • https://www.mathnet.ru/eng/mendc/v31/i2/p262
  • This publication is cited in the following 8 articles:
    1. Faeze Namayandeh Niasar, Mohsen Moradian, “Synthesis of some derivatives of 1,8-dioxo-octa-hydro xanthene and 9-aryl-hexahydro acridine-1,8-dione using metal ion-exchanged NaY zeolite as heterogeneous catalyst”, RSC Adv., 14:15 (2024), 10322  crossref
    2. L. Wang, M. Liu, J. Cheng, Knowledge Updates 2024/1, 2024  crossref
    3. Tatyana V. Balashova, Maxim V. Arsenyev, Svetlana K. Polyakova, Vasily A. Ilichev, Roman V. Rumyantcev, Georgy K. Fukin, Artem N. Yablonskiy, Mikhail N. Bochkarev, “New NIR-luminescent lanthanide complexes with tridentate oxybenzophenanthroline ligands”, New J. Chem., 47:19 (2023), 9164  crossref
    4. A. E. Tarakanova, N. D. Anisimova, D. A. Martynova, N. M. Khamaletdinova, E. V. Baranov, M. V. Arsenyev, S. A. Chesnokov, “Alkylation of Phenols with 4,6-Di-tert-butyl-3-methoxymethylcatechol. Antiradical Activity of Sterically Hindered Catecholphenols”, Russ J Gen Chem, 93:S3 (2023), S629  crossref
    5. D. V. Tsyganov, D. V. Demchuk, O. I. Adaeva, L. D. Konyushkin, M. E. Minyaev, V. N. Khrustalev, V. V. Semenov, “Synthesis and X-ray diffraction analysis of coenzyme Q derivatives obtained from natural polyalkoxyallylbenzenes”, Mendeleev Commun., 33:4 (2023), 539–542  mathnet  crossref
    6. M. P. Vlasenko, A. F. Pozharskii, O. P. Demidov, V. A. Ozeryanskii, G. S. Borodkin, “α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1,4-naphthoquinone nitrogen derivatives”, Mendeleev Commun., 33:2 (2023), 197–200  mathnet  crossref
    7. Ivan V. Smolyaninov, Daria A. Burmistrova, Maxim V. Arsenyev, Maria A. Polovinkina, Nadezhda P. Pomortseva, Georgy K. Fukin, Andrey I. Poddel'sky, Nadezhda T. Berberova, “Synthesis and Antioxidant Activity of New Catechol Thioethers with the Methylene Linker”, Molecules, 27:10 (2022), 3169  crossref
    8. T. V. Balashova, S. K. Polyakova, A. A. Kukinov, R. V. Rumyantsev, G. K. Fukin, V. A. Ilichev, Yu. A. Gracheva, T. A. Antonenko, E. R. Milaeva, M. N. Bochkarev, “Effect of the Nature of Substituents in the Oxyacridine Ligands on the Luminescence Properties and Cytotoxicity of the Zinc Complexes”, Russ J Coord Chem, 47:11 (2021), 730  crossref
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