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Yu. A. Strelenko
Researcher at Russian Academy of Sciences
Publications - 273
Citations - 1168
Yu. A. Strelenko is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Azoxy & Nuclear magnetic resonance spectroscopy. The author has an hindex of 16, co-authored 268 publications receiving 1042 citations.
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Selective reduction of the nitro group in the presence of the azoxy group. Synthesis of 2- (alkyl-NNO-azoxy)anilines
TL;DR: In this article, the presence of electron-withdrawing substituents at the azoxy group (for example, CO2Et) leads to a change in the direction of the reaction resulting in selective reduction of the Azoxy group to the hydrazo group.
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New regiospecific methods for the synthesis of N′-cyanodiazene N-oxides
S. G. Zlotin,N. V. Airapetova,E. A. Vinogradova,A. I. Podgurskii,Yu. A. Strelenko,O. A. Luk'yanov +5 more
TL;DR: In this article, new regiospecific methods have been developed for the synthesis of aliphatic, aromatic, and heterocyclic N′-cyanodiazene N-oxides based on the reactions of nitroso compounds.
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The role of ph in the synthesis of diaziridines
TL;DR: In the synthesis of diaziridines from amines, carbonyl compounds, and NaOCl in water, the yields of 1,2-dialkyldiaziridis and 1, 2,3-trisubstituted diazidines with electron-withdrawing substituents in the side chain are less sensitive to changes in pH than those of simple alkyl substituent.
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Synthesis of 4-R-3-(4-R1-5-R2-1,2,3-triazol-1-YL)furazans. 1. Azidofurazans in 1,3-dipolar cycloaddition reactions with substituted acetylenes
L. V. Batog,L. S. Konstantinova,V. Yu. Rozhkov,Yu. A. Strelenko,Oleg V. Lebedev,Lenor I. Khmel’nitskii +5 more
TL;DR: In this paper, the 1,3-dipolar cycloaddition of azidofurazans to substituted acetylenes has been studied and substituted 3-(1, 2, 3-triazol-l-yl)furazans have been synthesized.
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An unusual cascade of SN reactions of benzotetrazine 1,3-dioxide derivatives
TL;DR: An unusual cascade of S NAr reactions was discovered in the series of benzo-1,2,3,4-tetrazine 1,3-dioxides containing two adjacent nucleofuges X and Y in the benzene ring as discussed by the authors.