This article is cited in 19 scientific papers (total in 19 papers)
Communications
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
Abstract:
Alkylation of 1,3,5-trimethoxybenzene with 3,5-di-tert-butyl-6-methoxymethylcatechol affords new sterically hindered biscatechol, whose oxidation gives the corresponding bis-o-quinone. Its treatment with triphenylstibine leads to bis-triphenylantimony(v) bis-catecholate.
Document Type:
Article
Language: English
Citation:
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
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https://www.mathnet.ru/eng/mendc1669
https://www.mathnet.ru/eng/mendc/v28/i1/p76
This publication is cited in the following 19 articles:
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
I. V. Smolyaninov, D. A. Burmistrova, N. P. Pomortseva, M. A. Polovinkina, O. P. Demidov, N. R. Al'myasheva, A. I. Poddel'skii, N. T. Berberova, “Triphenylphosphine Thiolate Gold(I) Complexes with Redox-Active Schiff Bases: Synthesis, Electrochemical Properties, and Biological Activity”, Koordinacionnaâ himiâ, 49:9 (2023), 565
I. V. Smolyaninov, D. A. Burmistrova, N. P. Pomortseva, M. A. Polovinkina, O. P. Demidov, N. R. Al'myasheva, A. I. Poddel'skii, N. T. Berberova, “Triphenylphosphine Thiolate Gold(I) Complexes with Redox-Active Schiff Bases: Synthesis, Electrochemical Properties, and Biological Activity”, Russ J Coord Chem, 49:9 (2023), 577
Jason A. Smith, James N. Smith, Comprehensive Heterocyclic Chemistry IV, 2022, 433
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
Omar Coughlin, Sophie L. Benjamin, Comprehensive Coordination Chemistry III, 2021, 321
Andrey I. Poddel'sky, Ivan V. Smolyaninov, Nikolay O. Druzhkov, Georgy K. Fukin, “Heterometallic antimony(V)-zinc and antimony(V)-copper complexes comprising catecholate and diazadiene as redox active centers”, Journal of Organometallic Chemistry, 952 (2021), 121994
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
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
Ivan V. Smolyaninov, Andrey I. Poddel'sky, Susanna A. Smolyaninova, Maxim V. Arsenyev, Georgy K. Fukin, Nadezhda T. Berberova, “Polyfunctional Sterically Hindered Catechols with Additional Phenolic Group and Their Triphenylantimony(V) Catecholates: Synthesis, Structure, and Redox Properties”, Molecules, 25:8 (2020), 1770
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
V. V. Sharutin, A. I. Poddel'sky, O. K. Sharutina, “Aryl Compounds of Pentavalent Antimony: Syntheses, Reactions, and Structures”, Russ J Coord Chem, 46:10 (2020), 663
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
L. S. Okhlopkova, A. I. Poddel'sky, I. V. Smolyaninov, G. K. Fukin, “Triphenylantimony(V) Catecholates Based on 3,6-Di-tert-Butyl-2,5-Dihydroxy-1,4-Benzoquinone”, Russ J Coord Chem, 46:6 (2020), 386
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
V. V. Sharutin, O. K. Sharutina, Yu. O. Pupkova(Gubanova), A. S. Fominykh, O. S. Eltsov, “Synthesis and structure of a new tetranuclear macrocyclic antimony(v) complex”, Mendeleev Commun., 30:1 (2020), 97–99
Vladimir V. Sharutin, Olga K. Sharutina, Yulia O. Gubanova, Oleg S. Eltsov, “Dihydroxybenzoic acids as polydentate ligands in phenylantimony (V) complexes”, Inorganica Chimica Acta, 494 (2019), 211
Ludmila S. Okhlopkova, Andrey I. Poddel'sky, Ivan V. Smolyaninov, Georgy K. Fukin, Nadezhda T. Berberova, Vladimir K. Cherkasov, Gleb A. Abakumov, “Triphenylantimony(V) catecholato complexes with 4-(2,6-dimethylphenyliminomethyl)pyridine. Structure, redox properties: The influence of pyridine ligand”, Journal of Organometallic Chemistry, 897 (2019), 32
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
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