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Reconstructive Methodology in the Synthesis of 2-Aminopurine. / Neymash, Artyom; Ulomsky, Evgeny; Fedotov, Victor et al.
In: Molecules, Vol. 29, No. 1, 134, 2024.

Research output: Contribution to journal › Article › peer-review

Harvard

Neymash, A, Ulomsky, E, Fedotov, V, Aminov, S, Lyapustin, D, Gorbunov, E, Ishimnikov, VA, Slepukhin, P & Rusinov, V 2024, 'Reconstructive Methodology in the Synthesis of 2-Aminopurine', Molecules, vol. 29, no. 1, 134. https://doi.org/10.3390/molecules29010134

APA

Neymash, A., Ulomsky, E., Fedotov, V., Aminov, S., Lyapustin, D., Gorbunov, E., Ishimnikov, V. A., Slepukhin, P., & Rusinov, V. (2024). Reconstructive Methodology in the Synthesis of 2-Aminopurine. Molecules, 29(1), [134]. https://doi.org/10.3390/molecules29010134

Vancouver

Neymash A, Ulomsky E, Fedotov V, Aminov S, Lyapustin D, Gorbunov E et al. Reconstructive Methodology in the Synthesis of 2-Aminopurine. Molecules. 2024;29(1):134. doi: 10.3390/molecules29010134

Author

Neymash, Artyom ; Ulomsky, Evgeny ; Fedotov, Victor et al. / Reconstructive Methodology in the Synthesis of 2-Aminopurine. In: Molecules. 2024 ; Vol. 29, No. 1.

BibTeX

@article{e0baab4b0dbb4cb6975c73da7f2c8d57,
title = "Reconstructive Methodology in the Synthesis of 2-Aminopurine",
abstract = "A fundamentally new synthetic approach to the synthesis of 2-aminopurine has been developed. It consists in the combination of the creation of a condensed polyazotic heterocyclic tetrazolopyrimidine structure, its transformation into triaminopyrimidine, and its subsequent cyclization into 2-aminopurine. The structure of the obtained compounds was established based on spectral characteristics, and the structure of the intermediate compound 5 was established directly by X-ray diffraction analysis. {\textcopyright} 2023 by the authors.",
author = "Artyom Neymash and Evgeny Ulomsky and Victor Fedotov and Semen Aminov and Daniil Lyapustin and Evgeny Gorbunov and Ishimnikov, {Vladislav A.} and Pavel Slepukhin and Vladimir Rusinov",
note = "The research was financially supported by the Russian Science Foundation (Project No. 23-23-00642).",
year = "2024",
doi = "10.3390/molecules29010134",
language = "English",
volume = "29",
journal = "Molecules",
issn = "1420-3049",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "1",

}

RIS

TY - JOUR

T1 - Reconstructive Methodology in the Synthesis of 2-Aminopurine

AU - Neymash, Artyom

AU - Ulomsky, Evgeny

AU - Fedotov, Victor

AU - Aminov, Semen

AU - Lyapustin, Daniil

AU - Gorbunov, Evgeny

AU - Ishimnikov, Vladislav A.

AU - Slepukhin, Pavel

AU - Rusinov, Vladimir

N1 - The research was financially supported by the Russian Science Foundation (Project No. 23-23-00642).

PY - 2024

Y1 - 2024

N2 - A fundamentally new synthetic approach to the synthesis of 2-aminopurine has been developed. It consists in the combination of the creation of a condensed polyazotic heterocyclic tetrazolopyrimidine structure, its transformation into triaminopyrimidine, and its subsequent cyclization into 2-aminopurine. The structure of the obtained compounds was established based on spectral characteristics, and the structure of the intermediate compound 5 was established directly by X-ray diffraction analysis. © 2023 by the authors.

AB - A fundamentally new synthetic approach to the synthesis of 2-aminopurine has been developed. It consists in the combination of the creation of a condensed polyazotic heterocyclic tetrazolopyrimidine structure, its transformation into triaminopyrimidine, and its subsequent cyclization into 2-aminopurine. The structure of the obtained compounds was established based on spectral characteristics, and the structure of the intermediate compound 5 was established directly by X-ray diffraction analysis. © 2023 by the authors.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85181935705

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001140615800001

U2 - 10.3390/molecules29010134

DO - 10.3390/molecules29010134

M3 - Article

VL - 29

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 1

M1 - 134

ER -

ID: 51603738