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Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones. / Steparuk, Elena V.; Obydennov, Dmitrii L.; Sosnovskikh, Vyacheslav Y.
In: Molbank, Vol. 2023, No. 2, M1668, 2023.

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

Harvard

Steparuk, EV, Obydennov, DL & Sosnovskikh, VY 2023, 'Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones', Molbank, vol. 2023, no. 2, M1668. https://doi.org/10.3390/M1668

APA

Steparuk, E. V., Obydennov, D. L., & Sosnovskikh, V. Y. (2023). Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones. Molbank, 2023(2), [M1668]. https://doi.org/10.3390/M1668

Vancouver

Steparuk EV, Obydennov DL, Sosnovskikh VY. Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones. Molbank. 2023;2023(2):M1668. doi: 10.3390/M1668

Author

Steparuk, Elena V. ; Obydennov, Dmitrii L. ; Sosnovskikh, Vyacheslav Y. / Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones. In: Molbank. 2023 ; Vol. 2023, No. 2.

BibTeX

@article{5f19039e2b3340aea264207aaed6ce46,
title = "Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones",
abstract = "A two-stage synthesis of 5-aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones (56–66% overall yields) was carried out by refluxing 5-aroyl-3-(benzyloxy)-2-(het)aryl-4H-pyran-4-ones with ammonium acetate in AcOH and subsequent debenzylation. The prepared N-unsubstituted 4-pyridones exist in the pyridone tautomeric form. {\textcopyright} 2023 by the authors.",
author = "Steparuk, {Elena V.} and Obydennov, {Dmitrii L.} and Sosnovskikh, {Vyacheslav Y.}",
note = "This research was funded by the Russian Science Foundation, grant number 22-73-10236 (https://rscf.ru/project/22-73-10236/ (accessed on 24 April 2023)).",
year = "2023",
doi = "10.3390/M1668",
language = "English",
volume = "2023",
journal = "Molbank",
issn = "1422-8599",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "2",

}

RIS

TY - JOUR

T1 - Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones

AU - Steparuk, Elena V.

AU - Obydennov, Dmitrii L.

AU - Sosnovskikh, Vyacheslav Y.

N1 - This research was funded by the Russian Science Foundation, grant number 22-73-10236 (https://rscf.ru/project/22-73-10236/ (accessed on 24 April 2023)).

PY - 2023

Y1 - 2023

N2 - A two-stage synthesis of 5-aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones (56–66% overall yields) was carried out by refluxing 5-aroyl-3-(benzyloxy)-2-(het)aryl-4H-pyran-4-ones with ammonium acetate in AcOH and subsequent debenzylation. The prepared N-unsubstituted 4-pyridones exist in the pyridone tautomeric form. © 2023 by the authors.

AB - A two-stage synthesis of 5-aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones (56–66% overall yields) was carried out by refluxing 5-aroyl-3-(benzyloxy)-2-(het)aryl-4H-pyran-4-ones with ammonium acetate in AcOH and subsequent debenzylation. The prepared N-unsubstituted 4-pyridones exist in the pyridone tautomeric form. © 2023 by the authors.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85163774687

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001017254100001

U2 - 10.3390/M1668

DO - 10.3390/M1668

M3 - Article

VL - 2023

JO - Molbank

JF - Molbank

SN - 1422-8599

IS - 2

M1 - M1668

ER -

ID: 41528523