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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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Journal ArticleDOI
1,2-Bis(methylamino)ethane-1,2-diol dihydrochloride as a new precursor of 1,2,1",2"-tetramethyl-3,3"-bidiaziridine
TL;DR: In this article, the synthesis of 1,2-bis(methylamino)ethane-1, 2-diol dihydrochloride (5) as an example, it was demonstrated that aliphatic α-aminocarbinols can be stabilized as hydrochlorides.
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Stereochemistry of the homolytic heterocyclization of alkynes with 1,2-ethanedithol into 1,4-dithianes
E. I. Troyanskii,Yu. A. Strelenko,Dmitry V. Demchuk,V. V. Samoshin,A. I. Lutsenko,G. I. Nikishin +5 more
TL;DR: In this article, the homolytic heterocyclization of dialkyl and diaryl-acetylenes with 1,2-ethanedithiol leads stereoselectively to cis-2,3-disubstituted 1,4-dithianes.
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NMR spectra and structure of 4,7-dimethylpyridazino[4,5-c]furoxane N,N′-dioxide
Yu. A. Strelenko,Oleg A. Rakitin,Vladimir A. Ogurtsov,Tamara I. Godovikova,Lenor I. Khmel’nitskii +4 more
TL;DR: In this paper, NMR spectroscopy was used to confirm the structure of 4,7-dimethylpyridazino[4,5]furoxane N,N′-dioxide obtained by the oxidation of diacetylfuroxanes dioxide by nitrogen tetroxide.
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Synthesis of First Nonannulated 1,2,3,4-Tetrazine 1,3-Dioxides
A. Yu. Tyurin,Aleksandr M. Churakov,Yu. A. Strelenko,Maxim O. Ratnikov,Vladimir A. Tartakovsky +4 more
TL;DR: The structures of these first representatives of 1,2,3,4,4-tetrazines were confirmed by 13C and 14N NMR spectroscopy as mentioned in this paper.
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Reactions ofN-nitramines and their trimethylsilyl derivatives withN,N-bis(trimethylsilyloxy)enamines
TL;DR: In this article, trimethylsilyl derivatives of methyl- and ethylnitramine react as N-centered nucleophiles with 2-N,N-bis(trimethyl-Silyloxy)aminopropene to give trimethyl-symmetric derivatives of α-(N-nitro)alkylamino-substituted acetone oximes.