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Mendeleev Communications, 2019, Volume 29, Issue 1, Pages 50–52
DOI: https://doi.org/10.1016/j.mencom.2019.01.015
(Mi mendc1417)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

A catalyst-free one-step synthesis of N-pyrimidinyl amidines from endocyclic enamines and 4-azidopyrimidines

N. A. Beliaeva, T. V. Beryozkinaa, G. Lubecb, V. A. Bakuleva

a Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
b Paracelsus Medical University, Salzburg, Austria
Abstract: Novel N-pyrimidyl amidines of alycyclic acids were obtained in one step from of 4-azidopyrimidines and endocyclic enamines. The reaction mechanism involves [3 + 2]-addition of azide at the double bond followed by cleavage of thus formed 1,2,3-triazoline ring, and a contraction of alicycle.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.4 Mb)


Citation: N. A. Beliaev, T. V. Beryozkina, G. Lubec, V. A. Bakulev, “A catalyst-free one-step synthesis of N-pyrimidinyl amidines from endocyclic enamines and 4-azidopyrimidines”, Mendeleev Commun., 29:1 (2019), 50–52
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  • https://www.mathnet.ru/eng/mendc/v29/i1/p50
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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