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Mendeleev Communications, 2002, Volume 12, Issue 6, Pages 231–233
DOI: https://doi.org/10.1070/MC2002v012n06ABEH001688
(Mi mendc4177)
 

This article is cited in 4 scientific papers (total in 4 papers)

Consecutive substitution for three nitro groups in 1,3,5-trinitrobenzene under the action of benzotriazole and other nucleophiles

O. Yu. Sapozhnikov, M. D. Dutov, V. V. Kachala, S. A. Shevelev

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (81 kB) Citations (4)
Abstract: The N-benzotriazole unit and the nitro group are similar in the activating effect of nucleophilic substitution for an aromatic nitro group at the meta position; this fact makes it possible to replace consecutively all of the three nitro groups in 1,3,5-trinitrobenzene.
Document Type: Article
Language: English


Citation: O. Yu. Sapozhnikov, M. D. Dutov, V. V. Kachala, S. A. Shevelev, “Consecutive substitution for three nitro groups in 1,3,5-trinitrobenzene under the action of benzotriazole and other nucleophiles”, Mendeleev Commun., 12:6 (2002), 231–233
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  • https://www.mathnet.ru/eng/mendc/v12/i6/p231
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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