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Mendeleev Communications, 1991, Volume 1, Issue 2, Pages 46–47
DOI: https://doi.org/10.1070/MC1991v001n02ABEH000026
(Mi mendc5487)
 

This article is cited in 6 scientific papers (total in 6 papers)

Different Behaviour of Fervenulin 4-Oxide and 1,3-Dimethyllumazine 5-Oxide towards Nucleophiles

A. V. Gulevskayaa, A. F. Pozharskiia, S. V. Shorshnevb, V. V. Kuz'menkoc

a Department of Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
b Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
c Southern Federal University, Rostov-on-Don, Russian Federation
Full-text PDF (265 kB) Citations (6)
Abstract: Fervenulin 4-oxide reacts with secondary amines and carbanions to give derivatives of 1,3-dimethyl-5-nitroso-6-hydrazinouracil 9 and 10; under similar conditions 1,3-dimethyllumazine 5-oxide reacts with piperidine and morpholine to give products 14 in high yield, by nucleophilic substitution of hydrogen at C(6).
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Document Type: Article
Language: English


Citation: A. V. Gulevskaya, A. F. Pozharskii, S. V. Shorshnev, V. V. Kuz'menko, “Different Behaviour of Fervenulin 4-Oxide and 1,3-Dimethyllumazine 5-Oxide towards Nucleophiles”, Mendeleev Commun., 1:2 (1991), 46–47
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  • This publication is cited in the following 6 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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