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Mendeleev Communications, 2015, Volume 25, Issue 1, Pages 36–38
DOI: https://doi.org/10.1016/j.mencom.2015.01.013
(Mi mendc2292)
 

This article is cited in 30 scientific papers (total in 30 papers)

Communications

Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans

L. L. Fershtat, M. A. Epishina, A. S. Kulikov, N. N. Makhova

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Hetarylthiofuroxans were synthesized by nucleophilic substitution of the nitro group in 4-nitrofuroxans under the action of hetarylthiols in the DBU–MeCN system at room temperature, reactivity of 4-nitrofuroxans being dependent on the C(3)-substituent.
Document Type: Article
Language: English


Citation: L. L. Fershtat, M. A. Epishina, A. S. Kulikov, N. N. Makhova, “Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans”, Mendeleev Commun., 25:1 (2015), 36–38
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  • https://www.mathnet.ru/eng/mendc2292
  • https://www.mathnet.ru/eng/mendc/v25/i1/p36
  • This publication is cited in the following 30 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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