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Mendeleev Communications, 2020, Volume 30, Issue 6, Pages 714–716
DOI: https://doi.org/10.1016/j.mencom.2020.11.008
(Mi mendc1301)
 

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

Communications

4-Azidotetrahydroquinazoline derivatives in CuAAC reaction

A. A. Nazarovaa, K. N. Sedenkovaab, D. A. Vasilenkoa, Yu. K. Grishina, T. S. Kuznetsovaa, E. B. Averinaab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
Full-text PDF (252 kB) Citations (7)
Abstract: 4-Azido-2-methyltetrahydroquinazoline N-oxide cleanly undergoes the copper(i)-catalyzed azide–alkyne cycloaddition (CuAAC) reaction with alkynes to give new conjugates with pyrimidine N-oxide and triazole moieties. Its deoxygenated analogue, 4-azido-2-methyltetrahydroquinazoline, is inert in CuACC process due to the shift of imidoyl azide–tetrazole equilibrium towards the tetrazole tautomer.
Keywords: pyrimidines, triazoles, CuAAC, N-oxides, tautomers, azidopyrimidine N-oxides, quantum chemical calculations.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.7 Mb)


Citation: A. A. Nazarova, K. N. Sedenkova, D. A. Vasilenko, Yu. K. Grishin, T. S. Kuznetsova, E. B. Averina, “4-Azidotetrahydroquinazoline derivatives in CuAAC reaction”, Mendeleev Commun., 30:6 (2020), 714–716
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  • https://www.mathnet.ru/eng/mendc/v30/i6/p714
  • This publication is cited in the following 7 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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