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
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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
M. A. Zherebtsov, M. V. Arsenyev, S. A. Chesnokov, V. K. Cherkasov, “Synthesis of 1-Substituted
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5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalene-2,3-dione”, Russ J Org Chem, 56:3 (2020), 534
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
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)
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
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
Thomas H. Do, Seth N. Brown, “Mono- and bimetallic pentacoordinate silicon complexes of a chelating bis(catecholimine) ligand”, Dalton Trans., 48:30 (2019), 11565
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
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
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
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
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
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