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Mendeleev Communications, 2014, Volume 24, Issue 4, Pages 206–208
DOI: https://doi.org/10.1016/j.mencom.2014.06.005
(Mi mendc2524)
 

This article is cited in 2 scientific papers (total in 2 papers)

Communications

1,3-Dipolar cycloaddition of alkenes to 3-azido-3-deoxythymidine as a route to 3-deoxythymidin-3-yl derivatives

P. N. Solyeva, R. A. Novikovb, M. K. Kukhanovaa, M. V. Jaskoa

a V.A. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: 1,3-Cycloaddition of acrylonitrile, acrylamide, vinyl acetate and allyl alcohol to azido group of 3-azido-3-deoxythymidine under mild conditions afforded the corresponding adducts which were tested as inhibitors of HIV reverse transcriptase.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (4.9 Mb)


Citation: P. N. Solyev, R. A. Novikov, M. K. Kukhanova, M. V. Jasko, “1,3-Dipolar cycloaddition of alkenes to 3-azido-3-deoxythymidine as a route to 3-deoxythymidin-3-yl derivatives”, Mendeleev Commun., 24:4 (2014), 206–208
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  • https://www.mathnet.ru/eng/mendc/v24/i4/p206
  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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