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Mendeleev Communications, 2013, Volume 23, Issue 2, Pages 113–115
DOI: https://doi.org/10.1016/j.mencom.2013.03.022
(Mi mendc2634)
 

This article is cited in 10 scientific papers (total in 10 papers)

Microwave-assisted Alkylation of p-tert-butylcalix[4]arene Lower Rim: The Effect of Alkyl Halides

V. A. Burilovab, R. I. Nugmanovab, R. R. Ibragimovab, S. E. Solovievaa, I. S. Antipinab, A. I. Konovalovab

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
Abstract: Alkylation of p-tert-butylcalix[4]arenes with alkyl bromides or iodides under microwave irradiation affords mostly the corresponding distal disubstituted ethers, whereas in case of alkyl chlorides reasonable yields of monoethers were achieved.
Keywords: microwave synthesis, calixarene, supramolecular chemistry.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.5 Mb)


Citation: V. A. Burilov, R. I. Nugmanov, R. R. Ibragimova, S. E. Solovieva, I. S. Antipin, A. I. Konovalov, “Microwave-assisted Alkylation of p-tert-butylcalix[4]arene Lower Rim: The Effect of Alkyl Halides”, Mendeleev Commun., 23:2 (2013), 113–115
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  • https://www.mathnet.ru/eng/mendc/v23/i2/p113
  • This publication is cited in the following 10 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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