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Mendeleev Communications, 2011, Volume 21, Issue 2, Pages 108–109
DOI: https://doi.org/10.1016/j.mencom.2011.03.018
(Mi mendc2883)
 

This article is cited in 13 scientific papers (total in 13 papers)

Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides

I. Yavari, T. Sanaeishoar, L. Azad, M. Ghazvini

Department of Chemistry, Science and Research Branch, Islamic Azad Univeristy, Ponak, Tehran, Iran
Abstract: The zwitterionic 1:1 intermediates formed in the reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates are trapped by 2,4-thiazolidine-2,4-diones to afford N-functionalized 2,4-dioxothiazolidines containing a ketenimine moiety.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (179.3 Kb)


Citation: I. Yavari, T. Sanaeishoar, L. Azad, M. Ghazvini, “Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides”, Mendeleev Commun., 21:2 (2011), 108–109
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  • https://www.mathnet.ru/eng/mendc/v21/i2/p108
  • This publication is cited in the following 13 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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