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Mendeleev Communications, 2014, Volume 24, Issue 6, Page 345
DOI: https://doi.org/10.1016/j.mencom.2014.11.010
(Mi mendc2575)
 

This article is cited in 16 scientific papers (total in 16 papers)

Communications

A convenient synthesis of cyclopropane malonyl peroxide

A. O. Terent'ev, V. A. Vil', O. M. Mulina, K. K. Pivnitsky, G. I. Nikishin

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Cyclopropane-1,1-dicarbonyl peroxide was prepared in 85% yield by the reaction of diethyl cyclopropane-1,1-dicarboxylate with the urea hydrogen peroxide clathrate in the presence of methanesulfonic acid.
Document Type: Article
Language: English


Citation: A. O. Terent'ev, V. A. Vil', O. M. Mulina, K. K. Pivnitsky, G. I. Nikishin, “A convenient synthesis of cyclopropane malonyl peroxide”, Mendeleev Commun., 24:6 (2014), 345
Linking options:
  • https://www.mathnet.ru/eng/mendc2575
  • https://www.mathnet.ru/eng/mendc/v24/i6/p345
  • This publication is cited in the following 16 articles:
    1. Debkanta Bhattacharya, Armido Studer, “meta‐Hydroxylation of Pyridines, Quinolines, and Isoquinolines Using Dearomatized Intermediates”, Angewandte Chemie, 2025  crossref
    2. Debkanta Bhattacharya, Armido Studer, “meta‐Hydroxylation of Pyridines, Quinolines, and Isoquinolines Using Dearomatized Intermediates”, Angew Chem Int Ed, 2025  crossref
    3. Y. Barsegyan, V. A. Vil', N. C. O. Tomkinson, A. O. Terent'ev, Knowledge Updates 2022/1, 2022  crossref
    4. Vera A. Vil', Evgenii S. Gorlov, Alexander O. Terent'ev, “4,4′-(Butane-1,4-diyl)bis(4-methyl-1,2-dioxolane-3,5-dione)”, Molbank, 2022:4 (2022), M1497  crossref
    5. Vera A. Vil', Evgenii S. Gorlov, Bing Yu, Alexander O. Terent'ev, “Oxidative α-acyloxylation of acetals with cyclic diacyl peroxides”, Org. Chem. Front., 8:12 (2021), 3091  crossref
    6. Vera A. Vil', Evgenii S. Gorlov, Oleg V. Bityukov, Yana A. Barsegyan, Yulia E. Romanova, Valentina M. Merkulova, Alexander O. Terent'ev, “C-O coupling of Malonyl Peroxides with Enol Ethers via [5+2] Cycloaddition: Non‐Rubottom Oxidation”, Adv Synth Catal, 361:13 (2019), 3173  crossref
    7. O. V. Bityukov, V. A. Vil', N. V. Lukashin, A. G. Cherednichenko, G. I. Nikishin, A. O. Terent'ev, “Solvent-free silica gel mediated decarboxylation of C–O coupling products of β-diketones and β-oxo esters with malonyl peroxides”, Mendeleev Commun., 29:1 (2019), 55–56  mathnet  crossref
    8. Vera A. Vil', Gabriel dos Passos Gomes, Maria V. Ekimova, Konstantin A. Lyssenko, Mikhail A. Syroeshkin, Gennady I. Nikishin, Igor V. Alabugin, Alexander O. Terent'ev, “Five Roads That Converge at the Cyclic Peroxy-Criegee Intermediates: BF3-Catalyzed Synthesis of β-Hydroperoxy-β-peroxylactones”, J. Org. Chem., 83:21 (2018), 13427  crossref
    9. M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity”, Mendeleev Commun., 28:5 (2018), 505–507  mathnet  crossref
    10. V. P. Ananikov, D. B. Eremin, S. A. Yakukhnov, A. D. Dilman, V. V. Levin, M. P. Egorov, S. S. Karlov, L. M. Kustov, A. L. Tarasov, A. A. Greish, A. A. Shesterkina, A. M. Sakharov, Z. N. Nysenko, A. B. Sheremetev, A. Yu. Stakheev, I. S. Mashkovsky, A. Yu. Sukhorukov, S. L. Ioffe, A. O. Terent'ev, V. A. Vil', Yu. V. Tomilov, R. A. Novikov, S. G. Zlotin, A. S. Kucherenko, N. E. Ustyuzhanina, V. B. Krylov, Yu. E. Tsvetkov, M. L. Gening, N. E. Nifantiev, “Organic and hybrid systems: from science to practice”, Mendeleev Commun., 27:5 (2017), 425–438  mathnet  crossref
    11. M. A. Lapitskaya, V. A. Vil', L. L. Vasiljeva, E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Spontaneous reaction of malonyl peroxides with methanol”, Mendeleev Commun., 27:3 (2017), 243–245  mathnet  crossref
    12. Alexander O. Terent'ev, Vera A. Vil', Evgenii S. Gorlov, Gennady I. Nikishin, Kasimir K. Pivnitsky, Waldemar Adam, “Lanthanide-Catalyzed Oxyfunctionalization of 1,3-Diketones, Acetoacetic Esters, And Malonates by Oxidative C–O Coupling with Malonyl Peroxides”, J. Org. Chem., 81:3 (2016), 810  crossref
    13. Nicholas C. O. Tomkinson, Encyclopedia of Reagents for Organic Synthesis, 2016, 1  crossref
    14. Carla Alamillo-Ferrer, Marianna Karabourniotis-Sotti, Alan R. Kennedy, Matthew Campbell, Nicholas C. O. Tomkinson, “Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans”, Org. Lett., 18:13 (2016), 3102  crossref
    15. Andrei Dragan, D. Heulyn Jones, Alan R. Kennedy, Nicholas C. O. Tomkinson, “Stereoselective Synthesis of Alkylidene Phthalides”, Org. Lett., 18:13 (2016), 3086  crossref
    16. M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Alcoholysis of malonyl peroxides to give peracids”, Mendeleev Commun., 26:1 (2016), 14–15  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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