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Mendeleev Communications, 2016, Volume 26, Issue 1, Pages 14–15
DOI: https://doi.org/10.1016/j.mencom.2016.01.006
(Mi mendc2093)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

Alcoholysis of malonyl peroxides to give peracids

M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (195 kB) Citations (7)
Abstract: Potassium acetate catalyzed alcoholysis of spirocycloalkyl malonyl peroxides affords 1-alkoxycarbonylcycloalkane-1-percarboxylic acids which are suitable for epoxidation of olefins.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (443.8 Kb)


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc2093
  • https://www.mathnet.ru/eng/mendc/v26/i1/p14
  • This publication is cited in the following 7 articles:
    1. Igor V. Alabugin, Leah Kuhn, Michael G. Medvedev, Nikolai V. Krivoshchapov, Vera A. Vil', Ivan A. Yaremenko, Patricia Mehaffy, Meysam Yarie, Alexander O. Terent'ev, Mohammad Ali Zolfigol, “Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone”, Chem. Soc. Rev., 50:18 (2021), 10253  crossref
    2. 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
    3. 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
    4. 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
    5. Alexander O. Terent'ev, Vera A. Vil', Evgenii S. Gorlov, Olga N. Rusina, Alexander A. Korlyukov, Gennady I. Nikishin, Waldemar Adam, “Selective Oxidative Coupling of 3H‐Pyrazol‐3‐ones, Isoxazol‐5(2H)‐ones, Pyrazolidine‐3,5‐diones, and Barbituric Acids with Malonyl Peroxides: An Effective C‐O Functionalization”, ChemistrySelect, 2:11 (2017), 3334  crossref
    6. 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
    7. Margarita A. Lapitskaya, Vera A. Vil', Elena D. Daeva, Alexander O. Terent'ev, Kasimir K. Pivnitsky, “ChemInform Abstract: Alcoholysis of Malonyl Peroxides to Give Peracids.”, ChemInform, 47:24 (2016)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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