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Synthesis and reactivity of 1,2,4-oxadiazolium salts. / Il’in, Mikhail V.; Bolotin, Dmitrii S.

в: Chemistry of Heterocyclic Compounds, Том 56, № 7, 01.07.2020, стр. 824-828.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Il’in, MV & Bolotin, DS 2020, 'Synthesis and reactivity of 1,2,4-oxadiazolium salts', Chemistry of Heterocyclic Compounds, Том. 56, № 7, стр. 824-828. https://doi.org/10.1007/s10593-020-02738-w

APA

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Author

Il’in, Mikhail V. ; Bolotin, Dmitrii S. / Synthesis and reactivity of 1,2,4-oxadiazolium salts. в: Chemistry of Heterocyclic Compounds. 2020 ; Том 56, № 7. стр. 824-828.

BibTeX

@article{3e52f248a5c944d3bc608700b06ee749,
title = "Synthesis and reactivity of 1,2,4-oxadiazolium salts",
abstract = "This review summarizes the reports related to the chemistry of 1,2,4-oxadiazolium salts and published until 2020. Emphasis has been put on the information revealing convenient synthetic methods for the preparation of these specific organic compounds. Importantly, this review sheds the light on reactivity and thereby synthetic potential of 1,2,4-oxadiazolium salts.",
keywords = "1,2,4-oxadiazole, 1,2,4-oxadiazolium salt, electrophilic reactant, heterocycle, nucleophilic substitution, ROUTE, RING, REARRANGEMENTS",
author = "Il{\textquoteright}in, {Mikhail V.} and Bolotin, {Dmitrii S.}",
note = "Funding Information: This work was supported by the Russian Foundation for Basic Research (grant 18-33-20012). Publisher Copyright: {\textcopyright} 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2020",
month = jul,
day = "1",
doi = "10.1007/s10593-020-02738-w",
language = "English",
volume = "56",
pages = "824--828",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "7",

}

RIS

TY - JOUR

T1 - Synthesis and reactivity of 1,2,4-oxadiazolium salts

AU - Il’in, Mikhail V.

AU - Bolotin, Dmitrii S.

N1 - Funding Information: This work was supported by the Russian Foundation for Basic Research (grant 18-33-20012). Publisher Copyright: © 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2020/7/1

Y1 - 2020/7/1

N2 - This review summarizes the reports related to the chemistry of 1,2,4-oxadiazolium salts and published until 2020. Emphasis has been put on the information revealing convenient synthetic methods for the preparation of these specific organic compounds. Importantly, this review sheds the light on reactivity and thereby synthetic potential of 1,2,4-oxadiazolium salts.

AB - This review summarizes the reports related to the chemistry of 1,2,4-oxadiazolium salts and published until 2020. Emphasis has been put on the information revealing convenient synthetic methods for the preparation of these specific organic compounds. Importantly, this review sheds the light on reactivity and thereby synthetic potential of 1,2,4-oxadiazolium salts.

KW - 1,2,4-oxadiazole

KW - 1,2,4-oxadiazolium salt

KW - electrophilic reactant

KW - heterocycle

KW - nucleophilic substitution

KW - ROUTE

KW - RING

KW - REARRANGEMENTS

UR - http://www.scopus.com/inward/record.url?scp=85089693751&partnerID=8YFLogxK

U2 - 10.1007/s10593-020-02738-w

DO - 10.1007/s10593-020-02738-w

M3 - Article

AN - SCOPUS:85089693751

VL - 56

SP - 824

EP - 828

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 7

ER -

ID: 70789966