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Mendeleev Communications, 2020, Volume 30, Issue 5, Pages 607–609
DOI: https://doi.org/10.1016/j.mencom.2020.09.018
(Mi mendc1267)
 

This article is cited in 1 scientific paper (total in 1 paper)

Communications

Convenient synthesis of furo[2,3-c][1,2]dioxoles from 1-aryl-2-allylalkane-1,3-diones

A. T. Zdvizhkova, P. S. Radulovb, R. A. Novikovb, V. A. Tafeenkoc, V. V. Chernyshevcd, A. I. Ilovaiskyb, A. O. Terent'evb, G. I. Nikishinb

a Interbranch Engineering Center 'Composites of Russia', Bauman Moscow State University, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
d A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (229 kB) Citations (1)
Abstract: Treatment of 1-aryl-2-allylalkane-1,3-diones with I2/H2O2 system in the presence of catalytic amount of phosphomolybdic acid affords furo[2,3-c][1,2]dioxole derivatives. With other acidic catalysts such as BF3 · Et2O, SnCl4, H2SO4 or TsOH, mixtures with linear 4-acyloxy-2,5-diiodoalkan-1-ones are formed.
Keywords: furo[2,3-c][1,2]dioxoles, iodination, peroxides, cyclization, hydrogen peroxide, iodine, acetals, phosphomolybdic acid, catalysis.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.6 Mb)


Citation: A. T. Zdvizhkov, P. S. Radulov, R. A. Novikov, V. A. Tafeenko, V. V. Chernyshev, A. I. Ilovaisky, A. O. Terent'ev, G. I. Nikishin, “Convenient synthesis of furo[2,3-c][1,2]dioxoles from 1-aryl-2-allylalkane-1,3-diones”, Mendeleev Commun., 30:5 (2020), 607–609
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  • https://www.mathnet.ru/eng/mendc/v30/i5/p607
  • This publication is cited in the following 1 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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