Oxidative aromatization of 4,7-dihydro-6-nitroazolo[1,5-a] pyrimidines: Synthetic possibilities and limitations, mechanism of destruction, and the theoretical and experimental substantiation

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Oxidative aromatization of 4,7-dihydro-6-nitroazolo[1,5-a] pyrimidines: Synthetic possibilities and limitations, mechanism of destruction, and the theoretical and experimental substantiation. / Lyapustin, Daniil N.; Ulomsky, Evgeny N.; Balyakin, Ilya A. и др.
в: Molecules, Том 26, № 16, 4719, 02.08.2021.

Результаты исследований: Вклад в журнал › Статья › Рецензирование

BibTeX

@article{759b7ef78ebe46b0987d20c2d0d72094,

title = "Oxidative aromatization of 4,7-dihydro-6-nitroazolo[1,5-a] pyrimidines: Synthetic possibilities and limitations, mechanism of destruction, and the theoretical and experimental substantiation",

keywords = "Azolo[1,5-a]pyrimidines, Multicomponent reactions, Nitro compounds, Nitro-synthons, Oxidation, Oxidative destruction, Synthesis of heterocycles, multicomponent reactions, DESIGN, oxidation, nitro-synthons, SALTS, DISCOVERY, POTENT, azolo[1, synthesis of heterocycles, nitro compounds, AGENTS, INHIBITORS, oxidative destruction, DERIVATIVES, 5-a]pyrimidines",

author = "Lyapustin, {Daniil N.} and Ulomsky, {Evgeny N.} and Balyakin, {Ilya A.} and Shchepochkin, {Alexander V.} and Rusinov, {Vladimir L.} and Chupakhin, {Oleg N.}",

note = "Funding Information: Funding: The synthetic part was supported by the Ministry of Science and Higher Education of the Russian Federation, State Contract no FEUZ-2020-0058 (H687.42B.223/20). The electrochemical research and the quantum chemical calculations was funded by Russian Foundation for Basic Research (RFBR), project number 20-03-00814. Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",

year = "2021",

month = aug,

day = "2",

doi = "10.3390/molecules26164719",

language = "English",

volume = "26",

journal = "Molecules",

issn = "1420-3049",

publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",

number = "16",

}

RIS

TY - JOUR

T1 - Oxidative aromatization of 4,7-dihydro-6-nitroazolo[1,5-a] pyrimidines: Synthetic possibilities and limitations, mechanism of destruction, and the theoretical and experimental substantiation

AU - Lyapustin, Daniil N.

AU - Ulomsky, Evgeny N.

AU - Balyakin, Ilya A.

AU - Shchepochkin, Alexander V.

AU - Rusinov, Vladimir L.

AU - Chupakhin, Oleg N.

N1 - Funding Information: Funding: The synthetic part was supported by the Ministry of Science and Higher Education of the Russian Federation, State Contract no FEUZ-2020-0058 (H687.42B.223/20). The electrochemical research and the quantum chemical calculations was funded by Russian Foundation for Basic Research (RFBR), project number 20-03-00814. Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

PY - 2021/8/2

Y1 - 2021/8/2

KW - Azolo[1,5-a]pyrimidines

KW - Multicomponent reactions

KW - Nitro compounds

KW - Nitro-synthons

KW - Oxidation

KW - Oxidative destruction

KW - Synthesis of heterocycles

KW - multicomponent reactions

KW - DESIGN

KW - oxidation

KW - nitro-synthons

KW - SALTS

KW - DISCOVERY

KW - POTENT

KW - azolo[1

KW - synthesis of heterocycles

KW - nitro compounds

KW - AGENTS

KW - INHIBITORS

KW - oxidative destruction

KW - DERIVATIVES

KW - 5-a]pyrimidines

UR - http://www.scopus.com/inward/record.url?scp=85112029923&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000689880300001

UR - https://elibrary.ru/item.asp?id=46985470

U2 - 10.3390/molecules26164719

DO - 10.3390/molecules26164719

M3 - Article

AN - SCOPUS:85112029923

VL - 26

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 16

M1 - 4719

ER -

ID: 22979922