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Mendeleev Communications, 2019, Volume 29, Issue 1, Pages 91–93
DOI: https://doi.org/10.1016/j.mencom.2019.01.031
(Mi mendc1433)
 

This article is cited in 9 scientific papers (total in 9 papers)

Communications

Trans-etherification of catechol-type benzylic ether with diols as a route to new sterically hindered bis-catechols

E. R. Zhiganshina, M. V. Arsenyev, A. S. Shavyrin, E. V. Baranov, S. A. Chesnokov

G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhnii Novgorod, Russian Federation
Full-text PDF (319 kB) Citations (9)
Abstract: The trans-etherification of 4,6-di-tert-butyl-2,3-dihydroxybenzyl methyl ether with α,ω-alkanediols under mild conditions (CHCl3, 65°C) leads to new sterically hindered biscatechols in high yields. The molecular structures of three of them was determined by single-crystal X-ray diffraction.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.3 Mb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc1433
  • https://www.mathnet.ru/eng/mendc/v29/i1/p91
  • This publication is cited in the following 9 articles:
    1. Zhanpeng Jiang, Jingyi He, Huijie Li, Yiming Liu, Jiuyin Pang, Chuanpeng Li, Guiquan Jiang, “Straw Tar Epoxy Resin for Carbon Fiber-Reinforced Plastic: A Review”, Polymers, 16:17 (2024), 2433  crossref
    2. 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
    3. E. R. Zhiganshina, V. S. Lysenkov, T. I. Lopatina, M. V. Arsenyev, S. A. Chesnokov, “(Met)acrylate-Containing Sterically Hindered o-Benzoquinones for free Radical Polymerization”, High Energy Chem, 56:3 (2022), 163  crossref
    4. 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
    5. 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
    6. 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  mathnet  crossref
    7. Elnara Zhiganshina, Maxim Arsenyev, Alexey Konev, Yuri Chechet, Sergey Chesnokov, “Photopolymerization of OCDMA Dimetacrylate Initiated by 3,5-Di-tert-Butyl-o- Quinone and its Bis-O-Benzoquinone”, KEM, 869 (2020), 129  crossref
    8. 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
    9. 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
    Citing articles in Google Scholar: Russian citations, English citations
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