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Mendeleev Communications, 2018, Volume 28, Issue 1, Pages 76–78
DOI: https://doi.org/10.1016/j.mencom.2018.01.025
(Mi mendc1669)
 

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

M. V. Arsenyev, T. V. Astaf'eva, E. V. Baranov, A. I. Poddel'sky, S. A. Chesnokov

G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhnii Novgorod, Russian Federation
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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  • This publication is cited in the following 19 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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